Patent Application
20190185437
The present invention relates to compounds for use in treating, ameliorating and/or preventing neuromuscular disorders, including the reversal of drug-induced neuromuscular blockade. The compounds as defined herein preferably inhibit the ClC-1 ion channel. The invention further relates to methods of treating, preventing and/or ameliorating neuromuscular disorders, by administering said composition to a person in need thereof.
Walking, breathing, and eye movement are examples of essential everyday physiological activities that are powered by contractile activity of skeletal muscle. Skeletal muscles are inherently resting and contractile activity exclusively occurs in response to commands from the central nervous system. Such neuronal commands take the form of action potentials that travel from the brain to the muscle fibers in several steps. The neuromuscular junction (NMJ) is the highly specialized membrane area on muscle fibers where motor neurons come into close contact with the muscle fibers, and it is at NMJ that neurofnal action potentials are transmitted to muscular action potentials in a one-to-one fashion via synaptic transmission.
Neuromuscular transmission refers to the sequence of cellular events at the NMJ whereby an action potential in the lower motor neuron is transmitted to a corresponding action potential in a muscle fiber. When a neuronal action potential arrives at the pre-synaptic terminal it triggers influx of Ca2+ through voltage gated P/Q-type Ca2+ channels in the nerve terminal membrane. This influx causes a rise in cytosolic Ca2+ in the nerve terminal that triggers exocytosis of acetylcholine (ACh). Released ACh next diffuses across the synaptic cleft to activate nicotinic ACh receptors in the post-synaptic, muscle fiber membrane. Upon activation, ACh receptors convey an excitatory current flow of Na+ into the muscle fiber, which results in a local depolarization of the muscle fiber at the NMJ that is known as the endplate potential (EPP). If the EPP is sufficiently large, voltage gated Na+ channels in the muscle fiber will activate and an action potential in the muscle fiber will ensue. This action potential then propagates from NMJ throughout the muscle fiber and triggers the Ca2+ release from the sarcoplasmic reticulum. The released Ca2+ activates the contractile proteins within the muscle fibers thus resulting in contraction of the fiber.
Failure in the neuromuscular transmission can arise from both pre-synaptic dysfunction (Lambert Eaton syndrome, amyotrophic lateral sclerosis, spinal muscular atrophy) and as a result of post-synaptic dysfunction as occurs in myasthenia gravis. Failure to excite and/or propagate action potentials in muscle can also arise from reduced muscle excitability such as in critical illness myopathy (CIM). In Lambert Eaton syndrome, an autoimmune attack against the pre-synaptic P/Q-type Ca2+ channels results in markedly reduced Ca2+ influx into the nerve terminal during the pre-synaptic action potential and, consequently, a reduced release of ACh into the synaptic cleft. In myasthenia gravis the most common finding is an autoimmune attack on the post-synaptic membrane either against the nicotinic ACh receptors or the musk-receptor in the muscle fiber membrane. Congenital forms of myasthenia are also known. Common to disorders with neuromuscular transmission failure (Lambert Eaton syndrome, amyotrophic lateral sclerosis, spinal muscular atrophy and myasthenia gravis) is that the current flow generated by ACh receptor activation is markedly reduced, and EPPs therefore become insufficient to trigger muscle fiber action potentials. Neuromuscular blocking agents also reduce EPP by antagonizing ACh receptors. In CIM with reduced muscle excitability, the EPP may be of normal amplitude but they are still insufficient to trigger muscle fiber action potentials because the membrane potential threshold for action potential excitation has become more depolarized because of loss-of-function of voltage gated Na+ channels in the muscle fibers.
While ACh release (Lambert Eaton, amyotrophic lateral sclerosis, spinal muscular atrophy), ACh receptor function (myasthenia gravis, neuromuscular blockade) and function of voltage gated Na+ channels (CIM) are essential components in the synaptic transmission at NMJ, the magnitude of the EPP is also affected by inhibitory currents flowing in the NMJ region of muscle fibers. These currents tend to outbalance excitatory current through ACh receptors and, expectedly, they thereby tend to reduce EPP amplitude. The most important ion channel for carrying such inhibitory membrane currents in muscle fibers is the muscle-specific ClC-1 Cl− ion channel.
ACh esterase (AChE) inhibitors are traditionally used in the treatment of myasthenia gravis. This treatment leads to improvement in most patients but it is associated with side effects, some of which are serious. Because ACh is an import neurotransmitter in the autonomic nervous system, delaying it's breakdown can lead to gastric discomfort, diarrhea, salivation and muscle cramping. Overdosing is a serious concern as it can lead to muscle paralysis and respiratory failure, a situation commonly referred to as cholinergic crisis. Despite the serious side effects of AChE inhibitors, these drugs are today the treatment of choice for a number of disorders involving neuromuscular impairment. In patients where pyridostigmine (a parasympathomimetic and a reversible ACHE inhibitor) is insufficient, corticosteroid treatment (prednisone) and immunosuppressive treatment (azathioprine) is used. Plasma exchange can be used to obtain a fast but transient improvement.
Unfortunately, all of the currently employed myasthenia gravis drug regimens are associated with deleterious long-term consequences. In addition, the otherwise safe use of common drugs such as anti-infectives, cardiovascular drugs, anticholinergics, anticonvulsants, antirheumatics and others have been reported to worsen the symptoms of myasthenia gravis patients.
The ClC-1 ion channel is emerging as a target for potential drugs, although its potential has been largely unrealized.
The present inventors have identified a group of compounds that alleviate neuromuscular junction disorders through inhibition of ClC-1 channels.
Thus, for the first time, it has been found that compounds that inhibit the ClC-1 ion channels are capable of restoring neuromuscular transmission, as evidenced by the data generated by investigation of the compound set in biological models described herein. These compounds thus constitute a new group of drugs that can be used to treat or ameliorate muscle weakness and muscle fatigue in neuromuscular junction disorders caused by disease or by neuromuscular blocking agents.
The present invention thus concerns the use of ClC-1 ion channel inhibitors in the treatment of a range of conditions, such as reversal of block, ALS and myasthenic conditions, in which muscle activation by the nervous system is compromised and symptoms of weakness and fatigue are prominent.
In one aspect the invention concerns a composition comprising a compound of Formula (II):
In one aspect the invention concerns a method of treating, preventing and/or ameliorating a neuromuscular disorder, said method comprising administering a therapeutically effective amount of the composition as defined herein to a person in need thereof.
In one aspect the invention concerns use of a composition as defined herein, for the manufacture of a medicament for the treatment, prevention and/or amelioration of a neuromuscular disorder, and/or for reversing and/or amelioration of a neuromuscular blockade after surgery.
In one aspect the invention concerns a method of reversing and/or ameliorating a neuromuscular blockade after surgery, said method comprising administering a therapeutically effective amount of the composition as defined herein to a person in need thereof.
In one aspect the invention concerns a method for recovery of neuromuscular transmission, said method comprising administering a therapeutically effective amount of the composition as defined herein to a person in need thereof.
In one aspect the invention concerns a composition as defined herein for use in recovery of neuromuscular transmission.
In one aspect the invention concerns use of a composition as defined herein for the manufacture of a medicament for the recovery of neuromuscular transmission.
In one aspect, the invention concerns a compound of Formula (I.3.4):
In another aspect, the invention concerns a compound of Formula (I.3.4):
In yet another aspect, the invention concerns a composition comprising a compound as defined herein.
The term “halogen” means fluoro, chloro, bromo or iodo. “Halo” means halogen.
The terms “C1-3 alkyl” and “C1-5-alkyl” refers to a branched or unbranched alkyl group having from one to three or one to five carbon atoms respectively, including but not limited to methyl, ethyl, prop-1-yl, prop-2-yl, 2-methyl-prop-1-yl, 2-methyl-prop-2-yl, 2,2-dimethyl-prop-1-yl, but-1-yl, but-2-yl, 3-methyl-but-1-yl, 3-methyl-but-2-yl, pent-1-yl, pent-2-yl and pent-3-yl.
The term “C1-5-alkenyl” refers to a branched or unbranched alkenyl group having from one to five carbon atoms, two of which are connected by a double bond, including but not limited to ethenyl, propenyl, isopropenyl, butenyl, isobutenyl, pentenyl and isopentenyl.
The term “C1-5-alkynyl” to a branched or unbranched alkynyl group having from one to five carbon atoms, two of which are connected by a triple bond, including but not limited to ethynyl, propynyl, butynyl and pentynyl.
The term “—C(═O)—” refers to a carbonyl group and is used herein followed by a specification of the group connected thereto, such as for example the term “—C(═O)—C1-5 alkyl” which refers to a carbonyl group connected to a branched or unbranched alkyl group having from one to five carbon atoms, including but not limited to a carbonyl group connected to methyl, ethyl, prop-1-yl, prop-2-yl, 2-methyl-prop-1-yl, 2-methyl-prop-2-yl, 2,2-dimethyl-prop-1-yl, but-1-yl, but-2-yl, 3-methyl-but-1-yl, 3-methyl-but-2-yl, pent-1-yl, pent-2-yl or pent-3-yl.
The term “C3-5-cycloalkyl” refers to a group having three to five carbon atoms including a monocyclic or bicyclic carbocycle, including but not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclopropylmethyl, cyclopropylethyl and cyclobutylmethyl.
The term “C5-cycloalkenyl” refers to a group having five carbon atoms including a monocyclic or bicyclic carbocycle wherein two carbon atoms in the ring are connected by a double bond, including but not limited to cyclobutenylmethyl.
The term “5-6 membered heterocycle” refers to a group having five to six carbon atoms wherein between 1 and 3 carbon atoms in the ring have been replaced with a heteroatom selected from the group comprising nitrogen, sulphur and oxygen. Binding to the heterocycle may be at the position of the heteroatom or via a carbon atom of the heterocycle.
5-membered heterocycles include but are not limited to furan, thiophene, pyrrole, imidazole, pyrazole, oxazole, thiazole, isoxazole, isothiazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,5-oxadiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,5-thiadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole, dihydrofuran, dihydrothiophene, 3-pyrroline, 2-pyrroline, 2-imidazoline, 2-pyrazolidine, dihydro-oxazole, dihydro-thiazole, dihydro-isoxazole, dihydro-isothiazole, dihydro-1,2,3-triazole, dihydro-1,2,4-triazole, dihydro-1,2,5-oxadiazole, dihydro-1,2,3-oxadiazole, dihydro-1,2,4-oxadiazole, dihydro-1,3,4-oxadiazole, dihydro-1,2,5-thiadiazole, dihydro-1,2,4-thiadiazole, dihydro-1,2,3-thiadiazole, dihydro-1,3,4-thiadiazole, tetrahydrofuran, tetrahydrothiophene, pyrrolidine, imidazolidine, pyrazolidine, oxazolidine, thiazolidine, isoxazolidine, isothiazolidine, 1,2,3-triazolidine, 1,2,4-triazolidine, 1,2,5-oxadiazolidine, 1,2,3-oxadiazolidine, 1,3,4-oxadiazolidine, 1,2,5-thiadiazolidine, 1,2,3-thiadiazolidine, 1,3,4-thiadiazolidine, 1,2-oxathiolane, 1,3-oxathiolane, 2-oxazolidinone and 2-pyrrolidinone. 6-membered heterocycles include but are not limited to pyridine, pyrazine, pyrimidine, pyridazine, tetrahydropyran, thiane, piperidine, 1,4-dioxane, morpholine, 1,4-oxathiane, 1,4-diathiane and piperazine.
The term “8-10 membered bicyclic heterocycle” refers to a group having eight to ten heavy atoms in which two ring systems have been fused together, wherein between 1 and 3 carbon atoms in the ring have been replaced with a heteroatom selected from the group comprising nitrogen, sulphur and oxygen. Binding to the heterocycle may be at the position of the heteroatom or via a carbon atom of the heterocycle.
Examples of 8-membered bicyclic heterocycles include but are not limited to tetrahydro-4H-cyclopent[d]isoxazole, hexahydro-1H-pyrrolizine, 1,4-dihydropyrrolo[3,2-b]pyrrole, 1,6-dihydropyrrolo[2,3-b]pyrrole, 6H-furo[2,3-b]pyrrole, 4H-furo[3,2-b]pyrrole, 6H-thieno[2,3-b]pyrrole and 4H-thieno[3,2-b]pyrrole.
Examples of 9-membered bicyclic heterocycles include but are not limited to benzofuran, benzothiophene, indole, benzimidazole, indazole, benzothiazole, benzoxazole, 1,2-benzisoxazole, 1,2-benzisothiazole, benzotriazole, pyrrolopyridine, pyrazolopyridine and imidazopyridine.
Examples of 10-membered bicyclic heterocycles include but are not limited to quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, phthalazine and naphthyridine.
The term “C1-8-alk(en/yn)yl” means C1-8-alkyl, C2-8-alkenyl or C2-6-alkynyl; wherein:
The term “C3-6-cycloalk(en)yl” means C3-6-cycloalkyl or C3-6-cycloalkenyl, wherein:
The term “half-life” as used herein is the time it takes for the compound to lose one-half of its pharmacologic activity. The term “plasma half-life” is the time that it takes the compound to lose one-half of its pharmacologic activity in the blood plasma.
The term “treatment” refers to the combating of a disease or disorder. “Treatment” or “treating,” as used herein, includes any desirable effect on the symptoms or pathology of a disease or condition as described herein, and may include even minimal changes or improvements in one or more measurable markers of the disease or condition being treated. “Treatment” or “treating” does not necessarily indicate complete eradication or cure of the disease or condition, or associated symptoms thereof.
The term “amelioration” refers to moderation in the severity of the symptoms of a disease or condition. Improvement in a patient's condition, or the activity of making an effort to correct, or at least make more acceptable, conditions that are difficult to endure related to patient's conditions is considered “ameliorative” treatment.
The term “prevent” or “preventing” refers to precluding, averting, obviating, forestalling, stopping, or hindering something from happening, especially by advance action.
The term “reversal” or “reversing” refers to the ability of a compound to restore nerve-stimulated force in skeletal muscle exposed either ex vivo or in vivo to a non-depolarizing neuromuscular blocking agent or another pharmaceutical that is able to depress neuromuscular transmission
The term “ester hydrolysing reagent” refers to a chemical reagent which is capable of converting an ester functional group to a carboxylic acid with elimination of the alcohol moiety of the original ester, including but not limited to acid, base, a fluoride source, PBr3, PCl3 and lipase enzymes.
The term “non-depolarizing blockers” refers to pharmaceutical agents that antagonize the activation of acetylcholine receptors at the post-synaptic muscle fibre membrane by blocking the acetylcholine binding site on the receptor. These agents are used to block neuromuscular transmission and induce muscle paralysis in connection with surgery.
The term “recovery of force in muscle with neuromuscular dysfunction” refers to the ability of a compound to recover contractile force in nerve-stimulated healthy rat muscle after exposure to submaximal concentration of (115 nM) tubocurarine for 90 mins. Recovery of force is quantified as the percentage of the force prior to tubocurarine that is recovered by the compound.
The term “total membrane conductance (Gm)” is the electrophysiological measure of the ability of ions to cross the muscle fibre surface membrane. It reflects the function of ion channels that are active in resting muscle fibres of which ClC-1 is known to contribute around 80% in most animal species.
It is within the scope of the present invention to provide a composition for use in treating, ameliorating and/or preventing neuromuscular disorders characterized in that the neuromuscular function is reduced. As disclosed herein, inhibition of ClC-1 surprisingly improves or restores neuromuscular function. The compositions of the present invention comprise compounds capable of inhibiting the ClC-1 channel thereby improving or restoring neuromuscular function.
In one aspect, the invention relates to a composition comprising a compound of Formula (I):
In one embodiment A is a monocyclic or bicyclic aromatic or heteroaromatic ring. A may for example be a monocyclic ring comprising 5 to 6 carbon atoms or a bicyclic ring comprising 8 to 10 C-atoms. In one embodiment A is five-membered or six-membered aromatic ring. A can also be a five-membered or six-membered heteroaromatic ring. In a preferred embodiment A is phenyl or naphthyl.
The heteroaromatic ring may for example comprise S, O or N atoms. In one embodiment A is a five or six-membered aromatic ring comprising at least one N. In one embodiment A is a five-membered heteroaromatic ring comprising an S and four C atoms. In another embodiment A is a five-membered heteroaromatic ring comprising an O and four C atoms.
In one aspect, the invention concerns a composition comprising a compound of Formula (I.3.4):
In one aspect, the invention relates to a composition comprising a compound of Formula (I.3.4), wherein:
In one aspect, the invention concerns a compound of Formula (I.3.4):
In one aspect, the invention concerns a compound of Formula (I.3.4):
In one embodiment, the invention relates to a composition comprising a compound of Formula (II):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof;
wherein
Y is selected from the group consisting of O, NH, N—CH3, CH2, CH2—O, S and SO2. Thus Y may be O, NH, N—CH3, CH2, CH2—O, S or SO2. In one preferred embodiment Y is selected from the group consisting of O, NH, CH2, S, and SO2. In a particular embodiment Y is O.
X1, X2 and X3 are selected from the group consisting of, CH and N. In one embodiment X1 is N, X2 is N or X3 is N. In another preferred embodiment X1 is N. In particular embodiment X2 is N.
R4 is selected from the group consisting of H, C1-6-alk(en/yn)yl, C3-6-cycloalk(en)yl, —NR9—CO—R10, —NR10—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10, cyano, O—R11, fluorinated C1-3, nitro and halo, wherein R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl
In one embodiment R4 is selected from the group consisting of H, C1-6-alk(en/yn)yl and C3-6-cycloalk(en)yl. In an embodiment thereof R4 is selected from the group consisting of H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl, from the group consisting of H, C1-4-alk(en)yl and C3-6-cycloalk(en)yl or from the group consisting of H, C1-4-alkyl and C3-6-cycloalk(en)yl. In one embodiment R4 is selected from the group consisting of H and C1-4-alkyl.
In another embodiment R4 is selected from the group consisting of NR9—CO—R10, —NR10—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10 or O—R11, wherein R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl. R9, R10 and R11 may for example be independently selected from H and C1-4-alkyl or from the group consisting of H and C1-3-alkyl. In one embodiment R9, R10 and R11 are independently selected from H and —CH3.
In another embodiment R4 is selected from the group consisting of cyano, fluorinated C1-3, nitro and halo. In one embodiment R4 is selected from the group consisting of Cl, Br, I or F. In one embodiment R4 is selected from the group consisting of Cl and Br.
R4 can be located in either ortho- meta or para-position with respect to Y.
m can be 0, 1, 2, 3, 4 or 5. In one embodiment m is 0, 1, 2, 3 or 4, such as 0, 1, 2 or 3 or such as 0, 1 or 2. In another embodiment m is 0 or 1.
In one embodiment R1 and R2 are independently selected from the group consisting of OR3, SR5, S(O)R5, S(O)2R5, NR3, NR3C(O)R9, wherein
In one embodiment R3 and/or R5 is selected from the group consisting of H, C1-8-alk(en/yn)yl and C3-6-cycloalk(en)yl. In another embodiment R3 is selected from the group consisting of H, C1-6-alkyl and C3-7-cycloalkyl. In yet another embodiment R3 is selected from the group consisting of H, C1-6-alkyl, such as from the group consisting of H and C1-4-alkyl. In another embodiment R3 is selected from the group consisting of H and CH3.
In another embodiment R1 and R2 are independently selected from the group consisting of H, C1-8-alk(en/yn)yl and C3-6-cycloalk(en)yl. C1-8-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to three substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10, —S(O)R12, S(O)2R12, cyano, O—R11, fluorinated C1-3-alkyl, nitro and halo.
R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl It is appreciated that R1 is different from R2.
In a preferred embodiment R1 is selected from the group consisting of H and —CH3. In a more preferred embodiment R1 is H.
In one embodiment R1 is H and R2 is selected from the group consisting of H, C1-8-alk(en/yn)yl and C3-6-cycloalk(en)yl. C1-8-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to three substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10, —S(O)R12, S(O)2R12, cyano, O—R11, fluorinated C1-3-alkyl, nitro and halo, wherein R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
In another embodiment R1 is H and R2 is selected from the group consisting of H, C1-4-alk(en)yl, C3-6-cycloalk(en)yl, wherein said C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to two substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10, —S(O)R12, S(O)2R12, cyano, O—R11, fluorinated C1-3-alkyl, nitro and halo, wherein R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
In yet another embodiment R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl, C3-6-cycloalkyl and amino-C14-alkyl, wherein said C1-4-alkyl and C3-6-cycloalkyl may be substituted with O—R11, wherein R11 is as defined above. In a specific embodiment R11 is —CH3.
In one embodiment R1 and R2 are independently selected from the group consisting of H and CH3. In a preferred embodiment R1 is H and R2 is selected from the group consisting of H, C1-6-alkyl and C3-7-cycloalkyl. For example, R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl and C3-5-cycloalkyl. In a further preferred embodiment R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl. In a particular embodiment, R1 is H and R2 is selected from the group consisting of H, —CH3, —CH(CH3)2 and cyclopropyl. In an embodiment thereof R1 is H and R2 is —CH(CH3)2.
In a specific embodiment R2 is —CH(CH3)CH2—O—CH3. In particular, R1 is H and R2 is —CH(CH3)CH2—O—CH3.
In a preferred embodiment the compound is the S-enantiomer with respect to the C-atom to which R2 is bound.
R1 and R2 are in one embodiment linked to form a C3-6-cycloalk(en)yl or a halo-C3-6-cycloalk(en)yl. In one particular embodiment R1 and R2 are linked to form a C3-5-cycloalk(en)yl or a halo-C3-5-cycloalk(en)yl. In another embodiment R1 and R2 are linked to form a C3-4-cycloalk(en)yl or a halo-C3-4-cycloalk(en)yl. In a preferred embodiment R1 and R2 are linked to form a cyclopropyl or a halo-cyclopropyl. In a more preferred embodiment R1 and R2 are linked to form a cyclopropyl.
In one embodiment, the invention relates to a composition comprising a compound of Formula (II.4):
In a particular embodiment R1 is H and R2 is —CH(CH3)2 and wherein said compound is the S-enantiomer with respect to the C-atom to which R2 is bound as shown in formula (III):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof;
wherein, m, Y, X1, X2 and X3 and R4 are as defined above. For example X1 is N, X2 is N or X3 is N. In another embodiment X1, X2 and X3 is C. R4 may for example be selected from the group consisting of H, halo, cyano, —CHO, C1-4-alk(en)yl, halo-C1-4-alk(en)yl, —O—C1-4-alk(en)yl
In a preferred embodiment m is 0, 1 or 2. In one embodiment m is 0 or 1. For example m is 1.
In one embodiment, the invention relates to a compound of Formula (III.4):
In an embodiment of the present invention the compound of Formula (I) is further defined by Formula (IV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein A, R2 and R4 are as defined above. In one embodiment R2 is C1-6-alkyl or C3-7-cycloalkyl. For example A is a monocyclic ring such as a phenyl. It is preferred that R4 is in ortho- or meta position.
In one embodiment, the invention relates to a compound of Formula (IV.4):
Thus, in an embodiment thereof, the compound of Formula (IV) is further defined by Formula (V):
wherein R2 and R4 are as defined above.
In one embodiment, the invention relates to a compound of Formula (V.4):
In one embodiment thereof, the compound of Formula (V) is further defined by Formula (VI):
wherein R4 is as defined above. It is preferred the R4 is in ortho- or meta position.
In one embodiment, the invention relates to a compound of Formula (VI.4):
In another embodiment of the present invention the compound of Formula (I) is further defined by Formula (VII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m is 2 and X1, X2, Y, R2 and R4 are as defined above.
In one embodiment, the invention relates to a compound of Formula (VII.4):
In one embodiment thereof Formula (VII) is further defined by Formula (VIII)
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m, X2, Y, R2 and R4 are as defined above. For example, in a preferred embodiment Y is O. Further, it is preferred that R2 is selected from the group consisting of H and C1-4-alkyl. R4 is in one embodiment selected from the group consisting of H, —CH3 and halogen.
In one embodiment, the invention relates to a compound of Formula (VIII.4):
In a specific embodiment the compound of Formula (VIII) is further defined by Formula (IX):
In one embodiment, the invention relates to a compound of Formula (IX.4):
In one embodiment of the present invention the compound of Formula (VII) is further defined by Formula (X):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH(CH3)CH2—O—CH3, —CH2—CH2—CH3, —CH2—NH2, —CH2—CHF2, —CH2—CF3, —CH2—NH—CO—CH3 and —CH2—NH—SO2—CH3 and cyclopropyl, and R4 is selected from the group consisting of H, Br, Cl, F and I. In a preferred embodiment R2 is —CH3 or —CH(CH3)2; and R4 is selected from the group consisting of H, Br, Cl, F and I. In particular, R2 is —CH(CH3)2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
In one embodiment, the invention relates to a compound of Formula (X.4):
In one embodiment, the invention relates to a compound of Formula (XI.4):
In one embodiment, the invention relates to a compound of Formula (XII.4):
In one embodiment, the invention relates to a compound of Formula (XIII.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In specific embodiments Formula (VII) is further defined by any one of Formulas (XI) to (XXVIII):
In another embodiment of the present invention the compound of Formula (VII) is further defined by Formula (XXIX):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I. In a preferred embodiment R2 is —CH3 or —CH(CH3)2; and R4 is selected from the group consisting of H, Br, Cl, F and I. In another preferred embodiment R2 is —CH3 or —CH(CH3)2 and R4 is selected from the group consisting of H, Br, Cl and F. It is further preferred that the compound of Formula (X) is the S-enantiomer with respect to the C-atom to which R2 is bound. This embodiment is exemplified by Formulas (XXIII) and (XXIV), where R2 is —CH3 and R4 is Cl or Br.
Thus, in one embodiment the compound of Formula (XXIX) is further defined by Formula (XXX):
In another specific embodiment the compound of Formula (VII) is further defined by Formula (XXXI):
In one embodiment of the present invention Y is SO2. In particular, the compound of Formula (VII) can be further defined by Formula (XXXII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I. In a preferred embodiment R2 is —CH3 or —CH(CH3)2; and R4 is selected from the group consisting of H, Br, Cl, F and I. In another preferred embodiment R2 is —CH3 or —CH(CH3)2 and R4 is selected from the group consisting of H, Br, Cl and F.
In a specific embodiment the compound of Formula (XXXII) is defined by Formula (XXXIII):
As mentioned above, in one embodiment of the present A can be a naphthyl. In one embodiment Y is O. Thus, in a preferred embodiment of the present invention the compound of Formula (I) is further defined by Formula (XXXIV):
or a salt or tautomer thereof;
wherein R2 and X1 are as defined above; and R4 and R′4 are independently selected from the group consisting of H, halo, cyano, hydroxy, —CHO, C1-6-alk(en/yn)yl, halo-C1-6-alk(en/yn)yl, O—C1-6-alk(en/yn)yl. In a preferred embodiment R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2. Preferably R2 is CH3 or —CH(CH3)2. It is preferred that R4 and R′4 are individually selected from the group consisting of H, Br, Cl, F and I. In another preferred embodiment R4 and/or R′4 are H. It is further preferred that X1 is N or C.
In a particular embodiment R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2; X1 is N or C; and R4 and R′4 are individually selected from the group consisting of H, Br, Cl, F and I. In a particular embodiment Formula (XXXIV) is further defined by Formula (XXXV):
In specific embodiments of the present invention the compound of Formula (I) is further defined by any one of Formulas (XXXVI) to (LIX):
In a specific embodiment, the compound is selected from the group consisting of:
In one aspect, the invention relates to the use of the following compounds in treating, ameliorating and/or preventing a neuromuscular disorder. In one aspect, the invention relates to the use of the following compounds in reversing and/or ameliorating a neuromuscular blockade.
Another aspect of the present invention relates to a compound of Formula (I):
In one embodiment thereof, A is a monocyclic or bicyclic aromatic or heteroaromatic ring. For example, A can be a five-membered or six-membered aromatic ring. In one embodiment A is phenyl, or naphthyl.
In one aspect, the invention concerns a compound of Formula (I.3.4):
In one aspect, the invention relates to a compound of Formula (I.3.4), wherein:
In one aspect, the invention concerns a compound of Formula (I.3.4):
In one aspect, the invention concerns a compound of Formula (I.3.4):
In another embodiment of the present invention, the compound of Formula (I) is further defined by Formula (II):
In a preferred embodiment R1 is selected from the group consisting of H and —CH3. In a particular embodiment R1 is H.
Thus, in one embodiment R1 is H and R2 is selected from the group consisting of H, C1-4-alk(en)yl, C3-6-cycloalk(en)yl, wherein said C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to two substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, NR9R10, —S(O)R12, S(O)2R12, cyano, O—R11, fluorinated C1-3-alkyl, nitro and halo, wherein R9, R10 and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl
Thus, in another embodiment R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl, C3-6-cycloalkyl and amino-C1-4-alkyl, wherein said C1-4-alkyl and C3-6-cycloalkyl may be substituted with O—R11, wherein R11 is as defined above. In one embodiment R11 is —CH3. In another embodiment R2 is —CH(CH3)CH2—O—CH3.
In a preferred embodiment of the present invention R1 is H and R2 is selected from the group consisting of H, C1-6-alkyl and C3-7-cycloalkyl. For example, R1 is H and R2 is selected from the group consisting of H, —CH3, —CH(CH3)2 and cyclopropyl. In a particular embodiment, R1 is H and R2 is —CH(CH3)2.
It is preferred that R1 is different from R2.
It is appreciated that the compound as defined herein is the S-enantiomer with respect to the C-atom to which R2 is bound.
In one embodiment, the invention relates to a compound of Formula (II.4):
In one embodiment thereof, R1 is H and R2 is C1-6-alkyl or C3-7-cycloalkyl and wherein said compound is the S-enantiomer with respect to the C-atom to which R2 is bound as shown in Formula (III):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein, Y, X1, X2 and X3 and R4 are as defined above.
In one preferred embodiment of the invention, R4 is selected from the group consisting of H, halo, cyano, —CHO, C1-4-alk(en)yl, halo-C1-4-alk(en)yl, —O—C1-4-alk(en)yl.
In one embodiment m is 0, 1 or 2. For example m is 1.
In one embodiment of the invention X1 is N, X2 is N or X3 is N. In another embodiment X1, X2 and X3 is C.
In one embodiment, the invention relates to a compound of Formula (III.4):
The compound may in one embodiment be defined by Formula (I), which is further defined by Formula (IV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof;
wherein A, R2 and R4 are as defined above.
In one embodiment, the invention relates to a compound of Formula (IV.4):
Also, the compound of Formula (IV) can be further defined by Formula (V):
wherein R2 and R4 are as defined above. It is preferred that R2 is C1-6-alkyl or C3-7-cycloalkyl.
In one embodiment, the invention relates to a compound of Formula (V.4):
In one embodiment thereof, the compound of Formula (V) is further defined by Formula (VI):
wherein R4 is as defined above. Preferably, R4 is in ortho- or meta position.
In one embodiment, the invention relates to a compound of Formula (VI.4):
In one embodiment of the present invention the compound of Formula (I) is further defined by Formula (VII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m is 2 and X1, X2, Y, R2 and R4 are as defined above.
In one embodiment, the invention relates to a compound of Formula (VII.4):
In an embodiment thereof, the compound of Formula (VII) is further defined by Formula (VIII)
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m, X2, Y, R2 and R4 are as defined above.
In one embodiment, the invention relates to a compound of Formula (VIII.4):
In one preferred embodiment Y is O. It is further preferred that R2 is selected from the group consisting of H and C1-4-alkyl. Preferably, R4 is selected from the group consisting of H, —CH3 and halogen. Thus, in one embodiment the compound is further defined by Formula (IX):
In one embodiment, the invention relates to a compound of Formula (IX.4):
In one embodiment the compound of Formula (VII) is further defined by Formula (X):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH(CH3)CH2—O—CH3, —CH2—CH2—CH3, —CH2—NH2, —CH2—CHF2, —CH2—CF3, —CH2—NH—CO—CH3 and —CH2—NH—SO2—CH3 and cyclopropyl, and R4 is selected from the group consisting of H, Br, Cl, F and I.
In one embodiment, the invention relates to a compound of Formula (X.4):
In one embodiment, the invention relates to a compound of Formula (XI.4):
In one embodiment, the invention relates to a compound of Formula (XII.4):
In one embodiment, the invention relates to a compound of Formula (XIII.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In specific embodiments, the compound of Formula (VII) is further defined by any one of Formulas (XI) to (XXVIII) as defined herein.
Another embodiment of the present invention relates to a compound of Formula (VII) that is further defined by Formula (XXIX):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
In particular, the compound of Formula (XXIX) is further defined by Formula (XXX):
In one embodiment, the compound of Formula (VII) is further defined by Formula (XXXI):
Also, the compound of Formula (VII) can be further defined by Formula (XXXII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
Preferably, the compound of Formula (XXXII) is further defined by Formula (XXXIII):
In another embodiment of the present invention the compound of Formula (I) is further defined by Formula (XXXIV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2; X1 is N or C; and R4 and R′4 are individually selected from the group consisting of H, Br, Cl, F and I.
In particular, Formula (XXXIV) can be further defined by Formula (XXXV):
In specific embodiments of the present invention, the compound of Formula (I) is further defined by any one of Formulas (XXXVI) to (LIX) and compounds A-1 to A-29.
In one embodiment, the compound or the compound for use according to the present invention has been modified in order to increase its half-life when administered to a patient, in particular its plasma half-life.
In one embodiment, the compound or the compound for use according to the present invention further comprises a moiety conjugated to said compound, thus generating a moiety-conjugated compound. In one embodiment, said moiety-conjugated compound has a plasma and/or serum half-life being longer than the plasma and/or serum half-life of the non-moiety conjugated compound.
In one embodiment, the moiety conjugated to the compound or compound for use according to the present invention, is one or more type(s) of moieties selected from the group consisting of albumin, fatty acids, polyethylene glycol (PEG), acylation groups, antibodies and antibody fragments
The compositions and compounds of the present invention are used for treating, ameliorating and/or preventing a neuromuscular disorder, or reversing neuromuscular blockade caused by non-depolarizing neuromuscular blocker or antibiotic agent.
The inventors of the present invention have shown that inhibition of ClC-1 channels recovers neuromuscular transmission. ClC-1 function may therefore contribute to muscle weakness in conditions of compromised neuromuscular transmission.
Thus, in one embodiment of the present invention, the composition for use as described herein inhibits ClC-1 channels. Thus, it is appreciated that compounds of Formula (I) inhibit ClC-1 channels.
The neuromuscular disorder may also include neuromuscular dysfunctions.
Neuromuscular disorders include for example disorders with symptoms of muscle weakness and fatigue. Such disorders may include conditions with reduced neuromuscular transmission safety factor. In one embodiment the neuromuscular disorders are motor neuron disorders. Motor neuron disorders are disorders with reduced safety in the neuromuscular transmission. In one embodiment motor neuron disorders are selected from the group consisting of amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), X-linked spinal and bulbar muscular atrophy, Kennedy's disorder, multifocal motor neuropathy, Guillain-Barré syndrome, poliomyelitis and post-polio syndrome.
Thus, in one preferred embodiment of the present invention the neuromuscular disorder is ALS. In another preferred embodiment the neuromuscular disorder is SMA. In another preferred embodiment the neuromuscular disorder is Charcot-Marie tooth disease (CMT). In another preferred embodiment the neuromuscular disorder is sarcopenia. In yet another preferred embodiment, the neuromuscular disorder is critical illness myopathy (CIM).
As stated above the neuromuscular disorders include for example disorders with symptoms of muscle weakness and fatigue. Such disorder may for example include diabetes.
In one embodiment the composition of the present invention is used to prevent neuromuscular disorder. The composition may for example be used prophylactically against nerve gas that is known to cause symptoms of muscle weakness and fatigue.
In another embodiment the neuromuscular disorders is chronic fatigue syndrome. Chronic fatigue syndrome (CFS) is the common name for a medical condition characterized by debilitating symptoms, including fatigue that lasts for a minimum of six months in adults. CFS may also be referred to as systemic exertion intolerance disorder (SEID), myalgic encephalomyelitis (ME), post-viral fatigue syndrome (PVFS), chronic fatigue immune dysfunction syndrome (CFIDS), or by several other terms. Symptoms of CFS include malaise after exertion; unrefreshing sleep, widespread muscle and joint pain, physical exhaustion, and muscle weakness.
In a further embodiment the neuromuscular disorder is a critical illness polyneuropathy or CIM. Critical illness polyneuropathy and CIM are overlapping syndromes of widespread muscle weakness and neurological dysfunction developing in critically ill patients.
The neuromuscular disorder may also include metabolic myopathy and mitochondrial myopathy. Metabolic myopathies result from defects in biochemical metabolism that primarily affects muscle. These may include glycogen storage disorders, lipid storage disorder and 3-phosphocreatine stores disorder. Mitochondrial myopathy is a type of myopathy associated with mitochondrial disorder. Symptoms of mitochondrial myopathies include muscular and neurological problems such as muscle weakness, exercise intolerance, hearing loss and trouble with balance and coordination.
In a preferred embodiment the neuromuscular disorder is a myasthenic condition. Myasthenic conditions are characterized by muscle weakness and neuromuscular transmission failure. Congenital myasthenia gravis is an inherited neuromuscular disorder caused by defects of several types at the neuromuscular junction. Myasthenia gravis3 and Lambert-Eaton syndrome are also examples of myasthenic condition. Myasthenia gravis is either an autoimmune or congenital neuromuscular disorder that leads to fluctuating muscle weakness and fatigue. In the most common cases, muscle weakness is caused by circulating antibodies that block ACh receptors at the postsynaptic neuromuscular junction, inhibiting the excitatory effects of the neurotransmitter ACh on nicotinic Ach-receptors at neuromuscular junctions. Lambert-Eaton myasthenic syndrome (also known as LEMS, Lambert-Eaton syndrome, or Eaton-Lambert syndrome) is a rare autoimmune disorder that is characterized by muscle weakness of the limbs. It is the result of an autoimmune reaction in which antibodies are formed against presynaptic voltage-gated calcium channels, and likely other nerve terminal proteins, in the neuromuscular junction.
Thus, in one preferred embodiment of the present invention the neuromuscular disorder is myasthenia gravis. In another preferred embodiment the neuromuscular disorder is Lambert-Eaton syndrome.
Neuromuscular blockade is used in connection with surgery under general anaesthesia. Reversing agents are used for more rapid and safer recovery of muscle function after such blockade. Complications with excessive muscle weakness after blockade during surgery can result in delayed weaning from mechanical ventilation and respiratory complications after the surgery. Since such complications have pronounced effects on outcome of the surgery and future quality of life of patients, there is a need for improved reversing agents. Thus, in a preferred embodiment the neuromuscular disorder is muscle weakness caused by neuromuscular blockade after surgery. In another preferred embodiment of the present invention the composition is used for reversing and/or ameliorating neuromuscular blockade after surgery. Thus, one aspect of the present invention relates to a composition comprising a compound of Formula (I):
In one aspect, the invention concerns a compound of Formula (I.3.4):
In one aspect, the invention relates to a compound of Formula (I.3.4), wherein:
In one aspect, the invention concerns a compound of Formula (I):
In one aspect, the invention concerns a compound of Formula (I):
In one embodiment, the invention relates to a compound of Formula (II.4):
In one embodiment, the invention relates to a compound of Formula (III.4):
In one embodiment, the invention relates to a compound of Formula (IV.4):
In one embodiment, the invention relates to a compound of Formula (V.4):
In one embodiment, the invention relates to a compound of Formula (VI.4):
In one embodiment, the invention relates to a compound of Formula (VII.4):
In one embodiment, the invention relates to a compound of Formula (VIII.4):
In one embodiment, the invention relates to a compound of Formula (IX.4):
In one embodiment, the invention relates to a compound of Formula (X.4):
In one embodiment, the invention relates to a compound of Formula (XI.4):
In one embodiment, the invention relates to a compound of Formula (XII.4):
In one embodiment, the invention relates to a compound of Formula (XIII.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In one embodiment, the invention relates to a compound of Formula (XIV.4):
In one embodiment, the compound for use in treating, ameliorating and/or preventing a neuromuscular disorder, and/or for use in reversing and/or ameliorating a neuromuscular blockade is selected from the group consisting of:
In one embodiment, the compound or the compound for use according to the present invention has been modified in order to increase its half-life when administered to a patient, in particular its plasma half-life.
In one embodiment, the compound or the compound for use according to the present invention further comprises a moiety conjugated to said compound, thus generating a moiety-conjugated compound. In one embodiment, said moiety-conjugated compound has a plasma and/or serum half-life being longer than the plasma and/or serum half-life of the non-moiety conjugated compound.
In one embodiment, the moiety conjugated to the compound or compound for use according to the present invention, is one or more type(s) of moieties selected from the group consisting of albumin, fatty acids, polyethylene glycol (PEG), acylation groups, antibodies and antibody fragments.
Another aspect of the invention relates to a method of reversing and/or ameliorating a neuromuscular blockade after surgery, said method comprising administering a therapeutically effective amount of the composition as defined in any one of the embodiments herein below to a person in need thereof.
In yet another aspect, the present invention relates to use of a composition as defined herein, for the manufacture of a medicament for reversing and/or amelioration of a neuromuscular blockade after surgery.
The composition of the present invention may comprise further active ingredients/agents or other components to increase the efficiency of the composition. Thus, in one embodiment the composition further comprises at least one further active agent. It is appreciated that the active agent is suitable for treating, preventing or ameliorating said neuromuscular disorder.
The active agent is in a preferred embodiment an acetylcholine esterase inhibitor. Said acetylcholine esterase inhibitor may for example be selected from the group consisting of delta-9-tetrahydrocannabinol, carbamates, physostigmine, neostigmine, pyridostigmine, ambenonium, demecarium, rivastigmine, phenanthrene derivatives, galantamine, caffeine—noncompetitive, piperidines, donepezil, tacrine, edrophonium, huperzine, ladostigil, ungeremine and lactucopicrin.
Preferably the acetylcholine esterase inhibitor is selected from the group consisting of neostigmine, physostigmine and pyridostigmine. It is preferred that the acetylcholine esterase inhibitor is neostigmine or pyridostigmine.
The active agent may also be an immunosuppressive drug. Immunosuppressive drugs are drugs that suppress or reduce the strength of the body's immune system. They are also known as anti-rejection drugs. Immunosuppressive drugs include but are not limited to glucocorticoids, corticosteroids, cytostatics, antibodies and drugs acting on immunophilins. In one embodiment the active agent is prednisone.
The active agent may also be an agent that is used in anti-myotonic treatment. Such agents include for example blockers of voltage gated Na+ channels, and aminoglycosides.
The active agent may also be an agent for reversing a neuromuscular blockade after surgery. Such agents include for example neostigmine or suggammadex.
The active agent may also be an agent for increasing the Ca2+ sensitivity of the contractile filaments in muscle. Such agent includes tirasemtiv.
The active agent may also be an agent for increasing ACh release by blocking voltage gated K+ channels in the pre-synaptic terminal. Such agent includes 3,4-aminopyridine. As illustrated in example 4, combination therapy using C8 and 3,4-diaminopyridine resulted in an unexpected synergistic effect on recovery of neuromuscular transmission.
In one embodiment, a composition comprising the compound or the compound for use, according to the present invention, is provided. The composition according to the present invention is used for treating, ameliorating and/or preventing a neuromuscular disorder, and/or for use in reversing and/or ameliorating a neuromuscular blockade. Thus, it is preferred that the compositions and compounds described herein are pharmaceutically acceptable. In one embodiment the composition as described herein is in the form of a pharmaceutical formulation. In one embodiment, the composition as described herein further comprises a pharmaceutically acceptable carrier.
Accordingly, the present invention further provides a pharmaceutical formulation, which comprises a compound as disclosed herein and a pharmaceutically acceptable salt or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof, as herein defined, and a pharmaceutically acceptable carrier. Thus, in one embodiment the composition of the present invention further comprises a pharmaceutically acceptable carrier. The pharmaceutical formulations may be prepared by conventional techniques, e.g. as described in Remington: The Science and Practice of Pharmacy 2005, Lippincott, Williams & Wilkins.
The pharmaceutically acceptable carriers can be either solid or liquid. Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules. A solid carrier can be one or more excipients which may also act as diluents, flavoring agents, solubilizers, lubricants, suspending agents, binders, preservatives, wetting agents, tablet disintegrating agents, or an encapsulating material.
Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for oral administration. Such liquid forms include solutions, suspensions, and emulsions. These preparations may contain, in addition to the active component, colorants, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.
The compositions of the present invention may be formulated for parenteral administration and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion or in multi-dose containers, optionally with an added preservative. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, for example solutions in aqueous polyethylene glycol. Examples of oily or non-aqueous carriers, diluents, solvents or vehicles include propylene glycol, polyethylene glycol, vegetable oils (e.g., olive oil), and injectable organic esters (e.g., ethyl oleate), and may contain agents such as preserving, wetting, emulsifying or suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution for constitution before use with a suitable vehicle, e.g., sterile, pyrogen-free water.
In a preferred embodiment the compositions of the present invention is formulated for oral administration. Oral administration forms include solid form preparations including powders, tablets, drops, capsules, cachets, lozenges, and dispersible granules. Other forms suitable for oral administration may include liquid form preparations including emulsions, syrups, elixirs, aqueous solutions, aqueous suspensions, toothpaste, gel dentrifrice, chewing gum, or solid form preparations which are intended to be converted shortly before use to liquid form preparations, such as solutions, suspensions, and emulsions. In powders, the carrier is a finely divided solid which is a mixture with the finely divided active component.
In a preferred embodiment the composition as described herein is formulated in a tablet or capsule. In tablets, the active component is mixed with the carrier having the necessary binding capacity in suitable proportions and compacted in the shape and size desired. Suitable carriers are magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose, a low melting wax, cocoa butter, and the like.
Drops according to the present invention may comprise sterile or non-sterile aqueous or oil solutions or suspensions, and may be prepared by dissolving the active ingredient in a suitable aqueous solution, optionally including a bactericidal and/or fungicidal agent and/or any other suitable preservative, and optionally including a surface active agent. Suitable solvents for the preparation of an oily solution include glycerol, diluted alcohol and propylene glycol.
Emulsions may be prepared in solutions in aqueous propylene glycol solutions or may contain emulsifying agents such as lecithin, sorbitan monooleate, or acacia. Aqueous solutions can be prepared by dissolving the active component in water and adding suitable colorants, flavors, stabilizing and thickening agents. Aqueous suspensions can be prepared by dispersing the finely divided active component in water with viscous material, such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, and other well-known suspending agents.
The compositions of the present invention may also be formulated in a wide variety of formulations for parenteral administration.
For injections and infusions the formulations may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, for example solutions in aqueous polyethylene glycol. Alternatively, the composition may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution for constitution before use with a suitable vehicle, e.g., sterile, pyrogen-free water. The formulations can be presented in unit-dose or multi-dose sealed containers, such as ampoules, vials, pre-filled syringes, infusion bags, or can be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid excipient, for example, water, for injections, immediately prior to use. Extemporaneous injection solutions and suspensions can be prepared from sterile powders, granules, and tablets.
Examples of oily or non-aqueous carriers, diluents, solvents or vehicles include propylene glycol, polyethylene glycol, vegetable oils, and injectable organic esters, and may contain formulatory agents such as preserving, wetting, emulsifying or suspending, stabilizing and/or dispersing agents.
The formulations for injection will typically contain from about 0.5 to about 25% by weight of the active ingredient in solution.
The compounds may also be administered topically. Regions for topical administration include the skin surface and also mucous membrane tissues of the vagina, rectum, nose, mouth, and throat.
The topical composition will typically include a pharmaceutically acceptable carrier adapted for topical administration. Thus, the composition may take the form of a suspension, solution, ointment, lotion, sexual lubricant, cream, foam, aerosol, spray, suppository, implant, inhalant, tablet, capsule, dry powder, syrup, balm or lozenge, for example. Methods for preparing such compositions are well known in the pharmaceutical industry.
The compounds of the present invention may be formulated for topical administration to the epidermis as ointments, creams or lotions, or as a transdermal patch. They may be made by mixing the active ingredient in finely-divided or powdered form, alone or in solution or suspension in an aqueous or non-aqueous fluid, with the aid of suitable machinery, with a greasy or non-greasy base. The base may comprise hydrocarbons such as hard, soft or liquid paraffin, glycerol, beeswax, a metallic soap; a mucilage; an oil of natural origin or a fatty acid. The formulation may incorporate any suitable surface active agent such as an anionic, cationic or non-ionic surfactant such as a sorbitan ester or a polyoxyethylene derivative thereof. Suspending agents such as natural gums, cellulose derivatives or inorganic materials such as silicaceous silicas, and other ingredients such as lanolin, may also be included.
Lotions according to the present invention also include those suitable for application to the eye. An eye lotion may comprise a sterile aqueous solution optionally containing a bactericide.
Formulations for use in nasal, pulmonary and/or bronchial administration are normally administered as aerosols in order to ensure that the aerosolized dose actually reaches the mucous membranes of the nasal passages, bronchial tract or the lung. The term “aerosol particle” is used herein to describe the liquid or solid particle suitable for nasal, bronchial or pulmonary administration, i.e., that will reach the mucous membranes.
Typically aerosols are administered by use of a mechanical devices designed for pulmonary and/or bronchial delivery, including but not limited to nebulizers, metered dose inhalers, and powder inhalers. With regard to construction of the delivery device, any form of aerosolization known in the art, including but not limited to spray bottles, nebulization, atomization or pump aerosolization of a liquid formulation, and aerosolization of a dry powder formulation, can be used.
Liquid Aerosol Formulations in general contain a compound of the present invention in a pharmaceutically acceptable diluent. Pharmaceutically acceptable diluents include but are not limited to sterile water, saline, buffered saline, dextrose solution, and the like.
Formulations for dispensing from a powder inhaler device will normally comprise a finely divided dry powder containing pharmaceutical composition of the present invention (or derivative) and may also include a bulking agent, such as lactose, sorbitol, sucrose, or mannitol in amounts which facilitate dispersal of the powder from the device. Dry powder formulations for inhalation may also be formulated using powder-filled capsules, in particularly capsules the material of which is selected from among the synthetic plastics.
The formulation is formulated to the type of device employed and may involve the use of an appropriate propellant material, in addition to the usual diluents, adjuvants and/or carriers useful in therapy and known to the person skilled in the art. The propellant may be any propellant generally used in the art. Specific non-limiting examples of such useful propellants are a chlorofluorocarbon, a hydrofluorocarbon, a hydrochlorofluorocarbon, or a hydrocarbon.
The formulations of the present embodiment may also include other agents useful for pH maintenance, solution stabilization, or for the regulation of osmotic pressure.
The formulations of the present embodiment may also include other agents useful for pH maintenance, solution stabilization, or for the regulation of osmotic pressure.
The pharmaceutical agent-chemical modifier complexes described herein can be administered transdermally. Transdermal administration typically involves the delivery of a pharmaceutical agent for percutaneous passage of the drug into the systemic circulation of the patient. The skin sites include anatomic regions for transdermally administering the drug and include the forearm, abdomen, chest, back, buttock, mastoidal area, and the like.
Transdermal delivery is accomplished by exposing a source of the complex to a patient's skin for an extended period of time. Transdermal patches have the added advantage of providing controlled delivery of a pharmaceutical agent-chemical modifier complex to the body. Such dosage forms can be made by dissolving, dispersing, or otherwise incorporating the pharmaceutical agent-chemical modifier complex in a proper medium, such as an elastomeric matrix material. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate of such flux can be controlled by either providing a rate-controlling membrane or dispersing the compound in a polymer matrix or gel. For example, a simple adhesive patch can be prepared from a backing material and an acrylate adhesive.
As described herein above administration forms include but are not limited to oral, parental, topical, enteral, rectal or buccal administration.
In one embodiment the composition is administered or adapted for administration enterally, topically, parenterally or as part of a sustained release implant.
The parenteral administration may for example be intravenous, subcutaneous, intramuscular, intracranial or intraperitoneal. In a preferred embodiment the parental administration is intramuscular. Enteral administration includes oral, rectal, or buccal administration and may be sustained release, long acting or immediate relase. In one embodiment topical administration is dermal, epicutaneous, vaginal, intravesical, pulmonary, intranasal, intratracheal or as eye drops.
In another embodiment the composition is administered or adapted for administration subcutaneously or intravenously.
It is appreciated that the composition of the present invention comprises at least 30 wt. % compound, such as at least 25 wt. % compound, such as for example at least 20 wt. % compound, at least 15 wt. % compound, such as at least 25 wt. % compound, such as for example at least 20 wt. % compound, at least 15 wt. % compound, such as at least 10 wt. % compound, such as for example at least 8 wt. % compound, at least 5 wt. % compound, such as at least 4 wt. % compound, such as for example at least 3 wt. % compound, at least 2 wt. % compound, such as at least 1 wt. % compound, such as for example at least 0.5 wt. % compound or at least 0.5 wt. % compound. Wt. % is an abbreviation for weight percent.
The compound is any compound defined by Formula (I). Thus, the active ingredient can be any of the compounds defined by the formulas or embodiments presented herein.
In one embodiment the compound as described herein is to be administered in a dosage of from 1 μg/kg-30,000 μg/kg body weight, such as 1 μg/kg-7,500 μg/kg, such as 1 μg/kg-5,000 μg/kg, such as 1 μg/kg-2,000 μg/kg, such as 1 μg/kg-1,000 μg/kg, such as 1 μg/kg-700 μg/kg, such as 5 μg/kg-500 μg/kg, such as 10 μg/kg to 100 μg/kg bodyweight.
In another embodiment the compound as described herein is to be administered in a dosage of from 1 μg/kg-1,000 μg/kg body weight, such as 1 μg/kg-500 μg/kg, such as 1 μg/kg-250 μg/kg, such as 1 μg/kg-100 μg/kg, such as 1 μg/kg-50 μg/kg, such as 1 μg/kg to 10 μg/kg bodyweight.
In yet another embodiment the compound as described herein is to be administered in a dosage of from 10 μg/kg-30,000 μg/kg body weight, such as 10 μg/kg-7,500 μg/kg, such as 10 μg/kg-5,000 μg/kg, such as 10 μg/kg-2,000 μg/kg, such as 10 μg/kg-1,000 μg/kg, such as 10 μg/kg-700 μg/kg, such as 10 μg/kg-500 μg/kg, such as 10 μg/kg to 100 μg/kg bodyweight.
In one embodiment the administration of the composition as described herein is repeated at least 1, 2, 3, 4, 5 or 6 times weekly.
In another embodiment the administration is repeated at least 1-3 times weekly, such as 2-5 times weekly, such as 3-6 times weekly.
In a further embodiment the administration is repeated daily. The administration of the composition may for example be repeated 1, 2, 3, 4, 5, 6, 7 or 8 times daily. In one embodiment the administration is repeated 1 to 8 times daily, such as 2 to 5 times daily.
The compound as defined herein can be modified in order to increase its half-life when administered to a patient, in particular its plasma half-life.
The term “half-life” as used herein is the time it takes for the compound to lose one-half of its pharmacologic activity. The term “plasma half-life” is the time that it takes the compound to lose one-half of its pharmacologic activity in the blood plasma.
Modification of the compound to increase its half-life may for example include conjugation of a moiety that increases the half-life of the compound. Thus, in an embodiment the compound further comprises a moiety conjugated to said compound, thus generating a moiety-conjugated compound. It is preferred that the moiety-conjugated compound has a plasma and/or serum half-life being longer than the plasma and/or serum half-life of the non-moiety conjugated compound.
The moiety conjugated to the compound can for example be one or more type(s) of moieties selected from the group consisting of albumin, fatty acids, polyethylene glycol (PEG), acylation groups, antibodies and antibody fragments.
In one aspect the present invention relates to a method of treating, preventing and/or ameliorating a neuromuscular disorder, said method comprising administering a therapeutically effective amount of the compositions and compounds as defined herein to a person in need thereof.
In one aspect, the present invention relates to a method of reversing and/or ameliorating a neuromuscular blockade, said method comprising administering a therapeutically effective amount of the compound or the compound for use as defined herein to a person in need thereof.
In one aspect, the present invention relates to a method for recovery of neuromuscular transmission, said method comprising administering a therapeutically effective amount of the compound or the compound for use as defined herein to a person in need thereof.
The person in need thereof may be a person having a neuromuscular disorder or a person at risk of developing a neuromuscular disorder or a person having symptoms of muscle weakness and/or fatigue. In another embodiment the person in need thereof is a person with reduced neuromuscular transmission safety with prolonged recovery after neuromuscular blockade. Types of neuromuscular disorders are defined herein above. In a preferred embodiment the person has, amyotrophic lateral sclerosis, spinal muscular atrophy, myasthenia gravis or Lambert-Eaton syndrome.
A therapeutically effective amount is an amount that produces a therapeutic response or desired effect in the person taking it. Administration routes, formulations, forms and dosages are as defined herein above and throughout this specification.
The method of treatment may be combined with other methods that are known to treat, prevent and/or ameliorate neuromuscular disorders. The treatment method may for example be combined with administration of any of the agents mentioned herein above. In one embodiment the treatment is combined with administration of acetylcholine esterase inhibitor such as for example neostigmine or pyridostigmine.
Another aspect of the invention relates to use of a composition as defined herein, for the manufacture of a medicament for the treatment, prevention and/or amelioration of a neuromuscular disorder.
Another aspect relates to use of a composition as defined herein, for the manufacture of a medicament or a reversal agent for reversing and/or ameliorating a neuromuscular blockade after surgery.
In one aspect, the present invention relates to methods of manufacturing compounds or compounds for use according to formula (I).
One method for manufacturing the compounds or compounds for use according to the present invention comprises the steps of
and
A second method for manufacturing the compounds or compounds for use according to the present invention comprises the steps of
Yet a third method for manufacturing the compounds or compounds for use according to the present invention comprises the steps of
and
The compounds of formula (I) may be administered as a prodrug to modify the distribution, duration of efficacy or other properties. Conversion of the carboxylic acid group of compounds of formula (I) to an ester using ethanol to form the ethyl ester is an example of such prodrug. Preferred alcohols include low molecular weight alcohols, phenols and other aromatic alcohols, and fluorinated alcohols. In some cases, it is preferable to use an enol as the alcohol, for example 4-hydroxy-pent-3-ene-2-one. Alternatively, the prodrug may be the corresponding aldehyde, or an imine thereof. Again, these precursors can be expected to transform to the carboxylic acid in vivo. The prodrugs are administered using the same formulations and in the same dosage ranges as the compounds of formula (I).
In one aspect, said prodrug is defined by Formula (LX):
or a salt of tautomer thereof
wherein m, A, Z, R1, R2 and R4 are as defined above and wherein R14 is an aromatic or heteroaromatic ring selected from the group consisting of phenyl, pyrimidyl, pyridinyl, thiazolyl, oxadiazolyl and quinolyl, all aromatic and heteroaromatic groups optionally substituted by one or more R4
In one embodiment R14 is a phenyl substituted with methoxy, nitro, cyano, Cl, Br, I and/or F.
In one embodiment Formula (LX) is further defined by Formula (LXI):
In another embodiment of the present invention the prodrug is defined by Formula (LXII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof, wherein m, A, Z, R1, R2 and R4 are as defined above.
The prodrug can also be defined by Formula (LXIII):
wherein m, A, Z, R1, R2 and R4 are as defined above, and B is a 5- to 7-membered heterocyclic.
Embodiment 1 is a composition comprising a compound of Formula (I):
Embodiment 2 is a composition according to embodiment 1, wherein A is a monocyclic or bicyclic aromatic or heteroaromatic ring.
Embodiment 3 composition according to embodiments 1 and 2, wherein A is five-membered or six-membered aromatic ring.
Embodiment 4 composition according to embodiment 1 to 3, wherein A is phenyl, or naphthyl.
Embodiment 5 composition according to any of the preceding embodiments, wherein said compound is a compound of Formula (II):
Embodiment 6 is a composition for use according to any one of the preceding embodiments, wherein R1 is selected from the group consisting of H and —CH3.
Embodiment 7 is a composition according to any one of the preceding embodiments, wherein R1 is H.
Embodiment 8 is a composition for use according to any of the preceding embodiments, wherein R1 is H and R2 is selected from the group consisting of H, C1-4-alk(en)yl, C3-6-cycloalk(en)yl, wherein said C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to two substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, —NR9R10, —S(O)R12, —S(O)2R12, cyano, —O—R11, fluorinated C1-3-alkyl, nitro and halo, wherein R9, R10, and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl, whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
Embodiment 9 is a composition for use according to any of the preceding embodiments, wherein R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl, C3-6-cycloalkyl and amino-C1-4-alkyl, wherein said C1-4-alkyl and C3-6-cycloalkyl may be substituted with O—R11, wherein R11 is selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
Embodiment 10 is a composition for use according to embodiment 9, wherein R11 is —CH3.
Embodiment 11 is a composition for use according to embodiment 9, wherein R2 is —CH(CH3)CH2—O—CH3.
Embodiment 12 is a composition for use according to any of embodiments 1 to 7, wherein R1 is H and R2 is selected from the group consisting of H, C1-6-alkyl and C3-7-cycloalkyl.
Embodiment 13 is a composition for use according to any of the preceding embodiments, wherein R1 is H and R2 is selected from the group consisting of H, —CH3, —CH(CH3)2 and cyclopropyl.
Embodiment 14 is a composition for use according to any of the preceding embodiments, wherein R1 is H and R2 is —CH(CH3)2.
Embodiment 15 is composition for use according to any one of the preceding embodiments, wherein R1 is different from R2.
Embodiment 16 is a composition for use according to any one of the preceding embodiments, wherein said compound is an S-enantiomer with respect to the C-atom to which R2 is bound.
Embodiment 17 is a composition for use according to any embodiments 1 to 16, wherein R1 is H and R2 is C1-6-alkyl or C3-7-cycloalkyl and wherein said compound is an S-enantiomer with respect to the C-atom to which R2 is bound as shown in Formula (III):
Embodiment 18 is a composition for use according to any one of the preceding embodiments wherein R4 is selected from the group consisting of H, halo, cyano, —CHO, C1-4-alk(en)yl, halo-C1-4-alk(en)yl, —O—C1-4-alk(en)yl.
Embodiment 19 is a composition for use according to any one of the preceding embodiments wherein m is 0, 1 or 2.
Embodiment 20 is a composition for use according to any one of the preceding embodiments wherein m is 1.
Embodiment 21 is a composition for use according to any embodiments, wherein X1 is N, X2 is N or X3 is N.
Embodiment 22 is a composition for use according to any one of embodiments 5 to 20, wherein X1, X2 and X3 is C.
Embodiment 23 is a composition for use according to any one of embodiments 1 to 4, wherein the compound of Formula (I) is further defined by Formula (IV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof;
Embodiment 24 is a composition for use according to embodiment 23, wherein the compound of Formula (IV) is further defined by Formula (V):
Embodiment 25 is a composition for use according to embodiments 23, wherein R2 is C1-6-alkyl or C3-7-cycloalkyl.
Embodiment 26 is a composition for use according embodiment 25, wherein the compound of Formula (V) is further defined by Formula (VI):
Embodiment 27 is a composition for use according to any one of embodiments 24 to 26, wherein R4 is in ortho- or meta position.
Embodiment 28 is a composition for use according to embodiment 1, wherein the compound of Formula (I) is further defined by Formula (VII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein
Embodiment 29 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by Formula (VIII)
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein
Embodiment 30 is a composition for use according to any one of embodiment 5 to 29, wherein Y is O.
Embodiment 31 is a composition for use according to any one of embodiments 28 to 30, wherein R2 is selected from the group consisting of H and C1-4-alkyl.
Embodiment 32 is a composition for use according to any one of embodiments 28 to 31, wherein R4 is selected from the group consisting of H, —CH3 and halogen.
Embodiment 33 is a composition for use according to embodiment 32, wherein said compound is further defined by Formula (IX):
Embodiment 34 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by Formula (X):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH(CH3)CH2—O—CH3, —CH2—CH2—CH3, —CH2—NH2, —CH2—CHF2, —CH2—CF3, —CH2—NH—CO—CH3 and —CH2—NH—SO2—CH3 and cyclopropyl, and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 35 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by any one of Formulas (XI) to (XXVIII):
Embodiment 36 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by Formula (XXIX):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 37 is a composition for use according to embodiment 36, wherein the compound of Formula (XXIX) is further defined by Formula (XXX):
Embodiment 38 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by Formula (XXXI):
Embodiment 39 is a composition for use according to embodiment 28, wherein the compound of Formula (VII) is further defined by Formula (XXXII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 40 is a composition for use according to embodiment 39, wherein the compound of Formula (XXXII) is further defined by Formula (XXXIII):
Embodiment 41 is a composition for use according to embodiment 1, wherein the compound of Formula (I) is further defined by Formula (XXXIV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2; X1 is N or C; and R4 and R′4 are independently selected from the group consisting of H, Br, Cl, F and I.
Embodiment 42 is a composition for use according to embodiment 41, wherein Formula (XXXIV) is further defined by Formula (XXXV):
Embodiment 43 is a composition for use according to embodiment 1, wherein the compound of Formula (I) is further defined by any one of Formulas (XXXVI) to (LIX)
Embodiment 44 is a composition for use according to any one of the preceding embodiments wherein said prodrug is defined by Formula (LX):
Embodiment 45 is a prodrug according to embodiment 44, wherein R14 is a phenyl substituted with methoxy, nitro, cyano, Cl, Br, I and/or F.
Embodiment 46 is a prodrug according to embodiment 44, wherein Formula (LX) is further defined by Formula (LXI):
Embodiment 47 is a composition for use according to any one of embodiments 1 to 43, wherein said prodrug is defined by Formula (LXII):
Embodiment 48 is a composition for use according to any one of embodiments 1 to 43,
wherein said prodrug is defined by Formula (LXIII):
Embodiment 49 is a composition for use according to any one of embodiments 1 to 43, wherein said prodrug is defined by Formula (LXIV):
Embodiment 50 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is myasthenia gravis.
Embodiment 51 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is autoimmune myasthenia gravis.
Embodiment 52 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is congenital myasthenia gravis.
Embodiment 53 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is Lambert-Eaton Syndrome.
Embodiment 54 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is critical illness myopathy.
Embodiment 55 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is amyotrophic lateral sclerosis (ALS).
Embodiment 56 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is spinal muscular atrophy (SMA).
Embodiment 57 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is critical illness myopathy (CIM).
Embodiment 58 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is reversal diabetic polyneuropathy.
Embodiment 59 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder is selected from the group consisting of Guillain-Barré syndrome, poliomyelitis, post-polio syndrome, chronic fatigue syndrome, and critical illness polyneuropathy.
Embodiment 60 is a composition for use according to any one of the preceding embodiments, wherein the composition is for use in the treatment of symptoms of an indication selected from the group consisting of myasthenia gravis (such as autoimmune and congenital myasthenia gravis), Lambert-Eaton Syndrome, critical illness myopathy, amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), critical illness myopathy (CIM), reversal diabetic polyneuropathy, Guillain-Barré syndrome, poliomyelitis, post-polio syndrome, chronic fatigue syndrome, and critical illness polyneuropathy.
Embodiment 61 is a composition for use according to any one of the preceding embodiments wherein the neuromuscular disorder has been induced by a neuromuscular blocking agent.
Embodiment 62 is a composition for use according to any one of the preceding embodiments further comprising a pharmaceutically acceptable carrier.
Embodiment 63 is a composition for use according to any one of the preceding embodiments further comprising at least one further active agent.
Embodiment 64 is a composition for use according to any one of the preceding embodiments wherein said further active agent is suitable for treating, preventing or ameliorating said neuromuscular disorder.
Embodiment 65 is a composition for use according to any one of the preceding embodiments, wherein said further active agent is an acetylcholine esterase inhibitor.
Embodiment 66 is a composition for use according to embodiment 65, wherein said acetylcholine esterase inhibitor is selected from the group consisting of delta-9-tetrahydrocannabinol, carbamates, physostigmine, neostigmine, pyridostigmine, ambenonium, demecarium, rivastigmine, phenanthrene derivatives, galantamine, caffeine—noncompetitive, piperidines, donepezil, tacrine, edrophonium, huperzine, ladostigil, ungeremine and lactucopicrin.
Embodiment 67 is a composition for use according embodiment 65, wherein said acetylcholine esterase inhibitor is neostigmine or pyridostigmine.
Embodiment 68 is a composition for use according to any one of the preceding embodiments, wherein said further active agent is suggamadex.
Embodiment 69 is a composition for use according to any one of the preceding embodiments, wherein said further active agent is tirasemtiv.
Embodiment 70 is a composition for use according to any one of the preceding embodiments, wherein said further active agent is 3,4-aminopyridine.
Embodiment 71 is a composition for use according to any one of the preceding embodiments, wherein the composition is administered or adapted for administration enterally, topically, parenterally or as part of a sustained release implant.
Embodiment 72 is a composition for use according to any one of the preceding embodiments, wherein the parenteral administration is intravenous, subcutaneous, intramuscular, intracranial or intraperitoneal.
Embodiment 73 is a composition for use according to any one of the preceding embodiments, wherein the enteral administration is oral, rectal, or buccal.
Embodiment 74 is a composition for use according to any one of the preceding embodiments, wherein the topical administration is dermal, epicutaneous, vaginal, intravesical, pulmonary, intranasal, intratracheal or as eye drops.
Embodiment 75 is a composition for use according to any one of the preceding embodiments, wherein the composition is administered or adapted for administration subcutaneously or intravenously.
Embodiment 76 is a composition for use according to any one of the preceding embodiments, wherein the composition is formulated for oral administration.
Embodiment 77 is a composition for use according to any one of the preceding embodiments, wherein the composition is formulated in a tablet or capsule.
Embodiment 78 is a composition for use according to any one of the preceding embodiments, wherein said composition is to be administered in a dosage of from 1 μg/kg-10,000 μg/kg body weight, such as 1 μg/kg-7,500 μg/kg, such as 1 μg/kg-5,000 μg/kg, such as 1 μg/kg-2,000 μg/kg, such as 1 μg/kg-1,000 μg/kg, such as 1 μg/kg-700 μg/kg, such as 5 μg/kg-500 μg/kg, such as 10 μg/kg to 100 μg/kg bodyweight.
Embodiment 79 is a composition for use according to any one of the preceding embodiments, wherein said administration is repeated daily.
Embodiment 80 is a composition for use according to any one of the preceding embodiments, wherein said administration is repeated at least 1-3 times weekly, such as 2-5 times weekly, such as 3-6 times weekly.
Embodiment 81 is a composition for use according to any one of the preceding embodiments, wherein said administration is repeated 1 to 8 times daily, such as 2 to 5 times daily.
Embodiment 82 is a composition for use according to any one of the preceding embodiments, wherein said compound further has been modified in order to increase its half-life when administered to a patient, in particular its plasma half-life.
Embodiment 83 is a composition for use according to any one of the preceding embodiments, wherein said compound further comprises a moiety conjugated to said compound, thus generating a moiety-conjugated compound.
Embodiment 84 is a composition for use according to any one of the preceding embodiments, wherein the moiety-conjugated compound has a plasma and/or serum half-life being longer than the plasma and/or serum half-life of the non-moiety conjugated compound.
Embodiment 85 is a composition for use according to any one of the preceding embodiments, wherein the moiety conjugated to the compound is one or more type(s) of moieties selected from the group consisting of albumin, fatty acids, polyethylene glycol (PEG), acylation groups, antibodies and antibody fragments.
Embodiment 86 is a method of treating, preventing and/or ameliorating a neuromuscular disorder, said method comprising administering a therapeutically effective amount of the composition as defined in any one of the preceding embodiment to a person in need thereof.
Embodiment 87 is a method of using a composition as defined in any one of embodiments 1 to 85, for the manufacture of a medicament for the treatment, prevention and/or amelioration of a neuromuscular disorder.
Embodiment 88 is a composition comprising a compound of Formula (I):
Embodiment 89 is a method of reversing and/or ameliorating a neuromuscular blockade after surgery, said method comprising administering a therapeutically effective amount of the composition as defined in embodiment 88 to a person in need thereof.
Embodiment 90 is a method for recovery of neuromuscular transmission, said method comprising administering a therapeutically effective amount of the composition as defined in embodiment 88 to a person in need thereof.
Embodiment 91 is a method of using a composition as defined in embodiment 88, for the manufacture of a medicament for recovery of neuromuscular transmission.
Embodiment 92 is a compound of Formula (I):
Embodiment 93 is a compound according to embodiment 92, wherein A is a monocyclic or bicyclic aromatic or heteroaromatic ring.
Embodiment 94 is a compound according to any of embodiments 92 and 93, wherein A is five-membered or six-membered aromatic ring.
Embodiment 95 is a compound according to any one of embodiments 92 to 93, wherein A is phenyl, or naphthyl.
Embodiment 96 is a compound according to any of embodiments 92 to 95, wherein said compound is a compound of Formula (II):
Embodiment 97 is a compound according to any one of embodiments 92 to 96, wherein R1 is selected from the group consisting of —H and —CH3.
Embodiment 98 is a compound according to any one of embodiments 92 to 96, wherein R1 is H.
Embodiment 99 is a compound according to any of embodiments 92 to 98, wherein R1 is H and R2 is selected from the group consisting of H, C1-4-alk(en)yl, C3-6-cycloalk(en)yl, wherein said C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl may be substituted with up to two substituents selected from the group consisting of —NR9—CO—R10, —N(R10)2—SO2—R12, —CO—NR9R10, —SO2—NR9R10, —R13—O—R11, —NR9R10, —S(O)R12, S(O)2R12, cyano, —O—R11, fluorinated C1-3-alkyl, nitro and halo, wherein R9, R10, and R11 are independently selected from H, C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl, whereas R12 is selected from C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
Embodiment 100 is a compound according to any of embodiments 92 to 98, wherein R1 is H and R2 is selected from the group consisting of H, C1-4-alkyl, C3-6-cycloalkyl and amino-C14-alkyl, wherein said C1-4-alkyl and C3-6-cycloalkyl may be substituted with O—R11, wherein R11 is selected from H or C1-4-alk(en/yn)yl and C3-6-cycloalk(en)yl.
Embodiment 101 is a compound according to embodiment 100, wherein R11 is —CH3.
Embodiment 102 is a compound according to embodiment 100, wherein R2 is —CH(CH3)CH2—O—CH3.
Embodiment 103 is a compound according to any of embodiments 92 to 102, wherein R1 is H and R2 is selected from the group consisting of H, C1-6-alkyl and C3-7-cycloalkyl.
Embodiment 104 is a compound according to any of embodiments 92 to 102, wherein R1 is H and R2 is selected from the group consisting of H, —CH3, —CH(CH3)2 and cyclopropyl.
Embodiment 105 is a compound according to any one of embodiments 92 to 104, wherein R1 is H and R2 is —CH(CH3)2.
Embodiment 106 is a compound according to any one of embodiments 92 to 105, wherein R1 is different from R2.
Embodiment 107 is a compound according to any one of embodiments 92 to 106, wherein said compound is an S-enantiomer with respect to the C-atom to which R2 is bound.
Embodiment 108 is a compound according to any embodiments 92 to 107, wherein R1 is H and R2 is C1-6-alkyl or C3-7-cycloalkyl and wherein said compound is an S-enantiomer with respect to the C-atom to which R2 is bound as shown in Formula (III):
Embodiment 109 is a compound according to any one of embodiments 92 to 108, wherein R4 is selected from the group consisting of H, halo, cyano, —CHO, C1-4-alk(en)yl, halo-C1-4-alk(en)yl, —O—C1-4-alk(en)yl.
Embodiment 110 is a compound according to any one of embodiments 92 to 109, wherein m is 0, 1 or 2.
Embodiment 111 is a compound according to any one of embodiments 92 to 110, wherein m is 1.
Embodiment 112 is a compound according to any one of embodiments 92 to 111, wherein X1 is N, X2 is N or X3 is N.
Embodiment 113 is a compound according to any one of embodiments 92 to 111, wherein X1, X2 and X3 is C.
Embodiment 114 is a compound according to any one of embodiments 92 to 113, wherein the compound of Formula (I) is further defined by Formula (IV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein
Embodiment 115 is a compound according to embodiment 114, wherein the compound of Formula (IV) is further defined by Formula (V):
wherein R2 and R4 are as defined above.
Embodiment 116 is a compound according to embodiment 114 or embodiment 115, wherein R2 is C1-6-alkyl or C3-7-cycloalkyl.
Embodiment 117 is a compound according embodiment 115, wherein the compound of Formula (V) is further defined by Formula (VI):
wherein R4 is as defined above
Embodiment 118 is a compound according to any one of embodiments 115 to 117, wherein R4 is in ortho- or meta position.
Embodiment 119 is a compound according to embodiment 92, wherein the compound of Formula (I) is further defined by Formula (VII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m is 2 and X1, X2, Y, R2 and R4 are as defined above.
Embodiment 120 is a compound according to embodiment 119, wherein the compound of Formula (VII) is further defined by Formula (VIII)
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein m, X2, Y, R2 and R4 are as defined above.
Embodiment 121 is a compound according to any one of embodiments 92 to 120, wherein Y is O.
Embodiment 122 is a compound according to any one of embodiments 92 to 121, wherein R2 is selected from the group consisting of H and C1-4-alkyl.
Embodiment 123 is a compound according to any one of embodiments 92 to 122, wherein R4 is selected from the group consisting of H, —CH3 and halogen.
Embodiment 124 is a compound according to any one of embodiments 92 to 123, wherein said compound is further defined by Formula (IX):
Embodiment 125 is a compound according to embodiment 119, wherein the compound of Formula (VII) is further defined by Formula (X):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH(CH3)CH2—O—CH3, —CH2—CH2—CH3, —CH2—NH2, —CH2—CHF2, —CH2—CF3, —CH2—NH—CO—CH3 and —CH2—NH—SO2—CH3 and cyclopropyl, and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 126 is a compound se according to embodiment 119, wherein the compound of Formula (VII) is further defined by any one of Formulas (XI) to (XXVIII) as defined in embodiment 35.
Embodiment 127 is a compound according to embodiment 119, wherein the compound of Formula (VII) is further defined by Formula (XXIX):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 128 is a compound according to embodiment 127, wherein the compound of Formula (XXIX) is further defined by Formula (XXX):
Embodiment 129 is a compound according to embodiment 119, wherein the compound of Formula (VII) is further defined by Formula (XXXI):
Embodiment 130 is a compound according to embodiment 119, wherein the compound of Formula (VII) is further defined by Formula (XXXII):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2 and R4 is selected from the group consisting of H, Br, Cl, F and I.
Embodiment 131 is a compound according to embodiment 130, wherein the compound of Formula (XXXII) is further defined by Formula (XXXIII):
Embodiment 132 is a compound according to embodiment 92, wherein the compound of Formula (I) is further defined by Formula (XXXIV):
or a pharmaceutically acceptable salt, solvate, polymorph, or tautomer thereof; wherein R2 is selected from the group consisting of —CH3, —CH2—CH3, —CH(CH3)2, —C(CH3)3, —CH2—CH2—CH3 and —CH2—NH2; X1 is N or C; and R4 and R′4 are independently selected from the group consisting of H, Br, Cl, F and I.
Embodiment 133 is a compound according to embodiment 132, wherein Formula (XXXIV) is further defined by Formula (XXXV):
Embodiment 134 is a compound according to embodiment 92, wherein the compound of Formula (I) is further defined by any one of Formulas (XXXVI) to (LIX) as defined in embodiment 43.
Embodiment 135 is a compound of Formula (I.3.4):
Embodiment 136 is a compound according to any one of the preceding embodiments, wherein R2 is a 5-membered heterocycle which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 137 is a compound according to any one of the preceding embodiments, wherein R2 is a 6-membered heterocycle which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 138 is a compound according to any one of the preceding embodiments, wherein R2 is an 8-membered bicyclic heterocycle which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 139 is a compound according to any one of the preceding embodiments, wherein R2 is a 9-membered bicyclic heterocycle which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 140 is a compound according to any one of the preceding embodiments, wherein R2 is a 10-membered bicyclic heterocycle which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 141 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of furan, thiophene, pyrrole, imidazole, pyrazole, oxazole, thiazole, isoxazole, isothiazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,5-oxadiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,5-thiadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole, dihydrofuran, dihydrothiophene, 3-pyrroline, 2-pyrroline, 2-imidazoline, 2-pyrazolidine, dihydro-oxazole, dihydro-thiazole, dihydro-isoxazole, dihydro-isothiazole, dihydro-1,2,3-triazole, dihydro-1,2,4-triazole, dihydro-1,2,5-oxadiazole, dihydro-1,2,3-oxadiazole, dihydro-1,3,4-oxadiazole, dihydro-1,2,5-thiadiazole, dihydro-1,2,3-thiadiazole, dihydro-1,3,4-thiadiazole, tetrahydrofuran, tetrahydrothiophene, pyrrolidine, imidazolidine, pyrazolidine, oxazolidine, thiazolidine, isoxazolidine, isothiazolidine, 1,2,3-triazolidine, 1,2,4-triazolidine, 1,2,5-oxadiazolidine, 1,2,3-oxadiazolidine, 1,3,4-oxadiazolidine, 1,2,5-thiadiazolidine, 1,2,3-thiadiazolidine, 1,3,4-thiadiazolidine, 1,2-oxathiolane, 1,3-oxathiolane, 2-oxazolidinone and 2-pyrrolidinone.
Embodiment 142 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of furan, thiophene, pyrrole, imidazole, pyrazole, oxazole, thiazole, isoxazole, isothiazole, 1,2,3-triazole, 1,2,4-triazole, 1,2,5-oxadiazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,5-thiadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole and 1,3,4-thiadiazole.
Embodiment 143 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of thiophene, pyrrole, isoxazole, 1,2,4-oxadiazole and 1,3,4-oxadiazole.
Embodiment 144 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of isoxazol-5-yl and isoxazol-3-yl.
Embodiment 145 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of pyridine, pyrazine, pyrimidine, pyridazine, tetrahydropyran, thiane, piperidine, 1,4-dioxane, morpholine, 1,4-oxathiane, 1,4-diathiane and piperazine, wherein each of which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 146 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of tetrahydro-4H-cyclopent[d]isoxazole, hexahydro-1H-pyrrolizine, 1,4-dihydropyrrolo[3,2-b]pyrrole, 1,6-dihydropyrrolo[2,3-b]pyrrole, 6H-furo[2,3-b]pyrrole, 4H-furo[3,2-b]pyrrole, 6H-thieno[2,3-b]pyrrole and 4H-thieno[3,2-b]pyrrole, wherein each of which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 147 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of benzofuran, benzothiophene, indole, benzimidazole, indazole, benzothiazole, benzoxazole, 1,2-benzisoxazole, 1,2-benzisothiazole, benzotriazole, pyrrolopyridine, pyrazolopyridine and imidazopyridine, wherein each of which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 148 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, phthalazine and naphthyridine, wherein each of which may be optionally substituted with one or more, identical or different, substituents R6.
Embodiment 149 is a compound according to any one of the preceding embodiments, wherein R2 is selected from the group consisting of isoxazole, oxazole oxadiazole, benzothiazole, thiazole, imidazole, tetrahydrofuran, triazole, pyrazole, thiophene, wherein each of which may be optionally substituted with one or more, identical or different, substituents R6
Embodiment 150 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (II.4):
Embodiment 151 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (III.4):
Embodiment 152 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (IV.4):
Embodiment 153 is a compound according to any one of the preceding embodiment, wherein the compound is of Formula (V.4):
Embodiment 154 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (VI.4):
Embodiment 155 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (VII.4):
Embodiment 156 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (VIII.4):
Embodiment 157 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (IX.4):
Embodiment 158 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (X.4):
Embodiment 159 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (XI.4):
Embodiment 160 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (XII.4):
Embodiment 161 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (XIII.4):
Embodiment 162 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (XIV.4):
Embodiment 163 is a compound according to any one of the preceding embodiments, wherein the compound is of Formula (XV.4):
Embodiment 164 is a compound according to any of the preceding embodiments, wherein R2 is pyridine-2-yl.
Embodiment 165 is a compound according to any of the preceding embodiments, wherein R2 is 3aH,4H,5H,6H,6aH-cyclopenta[d][1,2]oxazol-3-yl.
Embodiment 166 is a compound according to any of the preceding embodiments, wherein R2 is 4,5-dihydro-1,2-oxazol-5-yl.
Embodiment 167 is a compound according to any of the preceding embodiments, wherein R2 is 1H-imidazol-4-yl.
Embodiment 168 is a compound according to any of the preceding embodiments, wherein R2 is 4H-1,2,4-triazol-3-yl.
Embodiment 169 is a compound according to any of the preceding embodiments, wherein n is 0.
Embodiment 170 is a compound according to any of the preceding embodiments, wherein n is 1.
Embodiment 171 is a compound according to any of the preceding embodiments, wherein n is 2.
Embodiment 172 is a compound according to any one of the preceding embodiments, wherein R3 is deuterium or tritium.
Embodiment 173 is a compound according to any one of the preceding embodiments, wherein R3 is F, Cl, Br or I.
Embodiment 174 is a compound according to any one of the preceding embodiments, wherein R3 is F.
Embodiment 175 is a compound according to any one of the preceding embodiments, wherein R4 is C1-5 alkyl optionally substituted with one or more, identical or different, substituents R7.
Embodiment 176 is a compound according to any one of the preceding embodiments, wherein R4 is selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, 1-ethylpropyl, 2-methylbutyl, pentyl, allyl, homo-allyl, vinyl, crotyl, butenyl, pentenyl, butadienyl, pentadienyl, ethynyl, propynyl, butynyl, pentynyl, cyclopropyl, cyclobutyl, cyclopentyl and cyclopentenyl optionally substituted with one or more, identical or different, substituents R7.
Embodiment 177 is a compound according to any one of the preceding embodiments, wherein R4 is methyl, ethyl, n-propyl or isopropyl, optionally substituted with one or more, identical or different, substituents R7.
Embodiment 178 is a compound according to any one of the preceding embodiments, wherein R4 is methyl.
Embodiment 179 is a compound according to any one of the preceding embodiments, wherein R4 is ethyl.
Embodiment 180 is a compound according to any one of the preceding embodiments, wherein R4 is n-propyl or isopropyl.
Embodiment 181 is a compound according to any one of the preceding embodiments, wherein R4 is C1-5 alkyl substituted with one or more F.
Embodiment 182 is a compound according to any one of the preceding embodiments, wherein R4 is selected from the group consisting of —CH2F, —CHF2, —CF3, —CH2CH2F, —CH2CHF2 and —CH2CF3.
Embodiment 183 is a compound according to any one of the preceding embodiments, wherein R4 is —CH2F.
Embodiment 184 is a compound according to any one of the preceding embodiments, wherein R5 is hydrogen.
Embodiment 185 is a compound according to any one of the preceding embodiments, wherein R5 is C1-5 alkyl.
Embodiment 186 is a compound according to any one of the preceding embodiments, wherein R5 is methyl or tert-butyl.
Embodiments 187 is a compound according to any one of the preceding embodiments, wherein m is 0.
Embodiment 188 is a compound according to any one of the preceding embodiments, wherein m is 1.
Embodiment 189 is a compound according to any one of the preceding embodiments, wherein m is 2.
Embodiment 190 is a compound according to any one of the preceding embodiments, wherein R6 is selected from the group consisting of C1-5 alkyl, C1-5 alkenyl, C1-5 alkynyl, C3-5 cycloalkyl and C5 cycloalkenyl, each of which may be optionally substituted with one or more halogens.
Embodiment 191 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkyl.
Embodiment 192 is a compound according to any one of the preceding embodiments, wherein R6 is methyl or isopropyl.
Embodiment 193 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkenyl.
Embodiment 194 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkynyl.
Embodiment 195 is a compound according to any one of the preceding embodiments, wherein R6 is C3-5 cycloalkyl.
Embodiment 196 is a compound according to any one of the preceding embodiments, wherein R6 is cyclopropyl.
Embodiment 197 is a compound according to any one of the preceding embodiments, wherein R6 is C5 cycloalkenyl.
Embodiment 198 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkyl substituted with one or more F.
Embodiment 199 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkenyl substituted with one or more F.
Embodiment 200 is a compound according to any one of the preceding embodiments, wherein R6 is C1-5 alkynyl substituted with one or more F.
Embodiment 201 is a compound according to any one of the preceding embodiments, wherein R6 is C3-5 cycloalkyl substituted with one or more F.
Embodiment 202 is a compound according to any one of the preceding embodiments, wherein R6 is C5 cycloalkenyl substituted with one or more F.
Embodiment 203 is a compound according to any one of the preceding embodiments, wherein the compound is selected from the group consisting of:
Embodiment 204 is a compound according to any one of the preceding embodiments, wherein the compound is selected from the group consisting of:
Embodiment 205 is a compound according to any one of the preceding embodiments, wherein the compound has activity on ClC-1 receptor.
Embodiment 206 is a compound according to any one of the preceding embodiments, wherein the compound is an inhibitor of the ClC-1 ion channel.
Embodiment 207 is a compound according to any one of the preceeding embodiments, wherein the EC50<50 μM, preferably <40 μM, more preferably <30 μM, more preferably <20 μM, more preferably <15 μM, even more preferably <10 μM and most preferably <5 μM.
Embodiment 208 is a compound according to any one of the preceding embodiments, wherein the recovery of force in muscles with neuromuscular dysfunction is >5%, preferably >10%, more preferably >15%, more preferably >20%, more preferably >25%, even more preferably >30% and most preferably >35%.
Embodiment 209 is a compound according to any one of the preceding embodiments, wherein the compound improves the recovered force in isolated rat soleus muscles after exposure to tubocurarine.
Embodiment 210 is a composition comprising the compound according to any one of the preceding embodiments.
Embodiment 211 is a composition according to any one of the preceding embodiments, wherein the composition is a pharmaceutical composition.
Embodiment 212 is a compound or the composition according to any one of the preceding embodiments, for use as a medicament.
Embodiment 213 is a composition according to any one of the preceding embodiments, wherein the composition further comprises a pharmaceutically acceptable carrier.
Embodiment 214 is a composition according to any one of the preceding embodiments, wherein the composition further comprises at least one further active agent.
Embodiment 215 is a composition according to any one of the preceding embodiments, wherein said further active agent is suitable for treating, preventing or ameliorating said neuromuscular disorder.
Embodiment 216 is a composition according to any one of the preceding embodiments, wherein said further active agent is an acetylcholine esterase inhibitor.
Embodiment 217 is a composition according to any one of the preceding embodiments, wherein said acetylcholine esterase inhibitor is selected from the group consisting of delta-9-tetrahydrocannabinol, carbamates, physostigmine, neostigmine, pyridostigmine, ambenonium, demecarium, rivastigmine, phenanthrene derivatives, galantamine, caffeine—noncompetitive, piperidines, donepezil, tacrine, edrophonium, huperzine, ladostigil, ungeremine and lactucopicrin.
Embodiment 218 is a composition according to any one of the preceding embodiments, wherein said acetylcholine esterase inhibitor is neostigmine or pyridostigmine.
Embodiment 219 is a composition according to any one of the preceding embodiments, wherein said further active agent is suggamadex.
Embodiment 220 is a composition according to any one of the preceding embodiments, wherein said further active agent is tirasemtiv or CK-2127107.
Embodiment 221 is a composition according to any one of the preceding embodiments, wherein said further active agent is 3,4-aminopyridine.
Embodiment 222 is a method for manufacturing the compound according to any one of the preceding embodiments, the method comprising the steps of
and
Embodiment 223 is a method for manufacturing the compound according to any one of the preceding embodiments, the method comprising the steps of
Embodiment 224 is a method for manufacturing the compound according to any one of the preceding embodiments, the method comprising the steps of
and
Embodiment 225 is a compound according to any one of the preceding embodiments for use in treating, ameliorating and/or preventing a neuromuscular disorder, and/or for use in reversing and/or ameliorating a
Embodiment 226 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is myasthenia gravis.
Embodiment 227 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is autoimmune myasthenia gravis.
Embodiment 228 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is congenital myasthenia gravis.
Embodiment 229 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is Lambert-Eaton Syndrome.
Embodiment 230 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is critical illness myopathy.
Embodiment 231 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is amyotrophic lateral sclerosis (ALS).
Embodiment 232 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is spinal muscular atrophy (SMA).
Embodiment 233 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is critical illness myopathy (CIM).
Embodiment 234 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is Charcot-Marie tooth disease (CMT).
Embodiment 235 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is sarcopenia.
Embodiment 236 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is reversal diabetic polyneuropathy.
Embodiment 237 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder is selected from the group consisting of Guillain-Barré syndrome, poliomyelitis, post-polio syndrome, chronic fatigue syndrome, and critical illness polyneuropathy.
Embodiment 238 is a compound for use according to any one of the preceding embodiments, wherein the compound is for use in the treatment of symptoms of an indication selected from the group consisting of myasthenia gravis (such as autoimmune and congenital myasthenia gravis), Lambert-Eaton Syndrome, critical illness myopathy, amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), critical illness myopathy (CIM), reversal diabetic polyneuropathy, Guillain-Barré syndrome, poliomyelitis, post-polio syndrome, chronic fatigue syndrome, and critical illness polyneuropathy.
Embodiment 239 is a compound for use according to any one of the preceding embodiments wherein the neuromuscular disorder has been induced by a neuromuscular blocking agent.
Embodiment 240 is a compound for use according to any one of the preceding embodiments, wherein the neuromuscular blockade is neuromuscular blockade after surgery.
Embodiment 241 is a compound for use according to any one of the preceding embodiments, wherein the neuromuscular blockade is drug induced.
Embodiment 242 is a compound for use according to any one of the preceding embodiments, wherein the drug is an antibiotic.
Embodiment 243 is a compound for use according to any one of the preceding embodiments, wherein the drug is a non-depolarizing neuromuscular blocker.
Embodiment 244 is a compound for use according to any one of the preceding embodiments, wherein said compound further has been modified in order to increase its half-life when administered to a patient, in particular its plasma half-life.
Embodiment 245 is a compound for use according to any one of the preceding embodiments, wherein said compound further comprises a moiety conjugated to said compound, thus generating a moiety-conjugated compound.
Embodiment 246 is a compound for use according to any one of the preceding embodiments, wherein the moiety-conjugated compound has a plasma and/or serum half-life being longer than the plasma and/or serum half-life of the non-moiety conjugated compound.
Embodiment 247 is a compound for use according to any one of the preceding embodiments, wherein the moiety conjugated to the compound is one or more type(s) of moieties selected from the group consisting of albumin, fatty acids, polyethylene glycol (PEG), acylation groups, antibodies and antibody fragments.
Embodiment 248 is a compound for use according to any one of the preceding embodiments, wherein said compound is comprised in a composition.
Embodiment 249 is a compound for use according to any one of the preceding embodiments, wherein the composition is a pharmaceutical composition.
Embodiment 250 is a compound for use according to any one of the preceding embodiments, wherein the composition further comprises a pharmaceutically acceptable carrier.
Embodiment 251 is a compound for use according to any one of embodiments, wherein the composition further comprises at least one further active agent.
Embodiment 252 is a compound for use according to any one of the preceding embodiments, wherein said further active agent is suitable for treating, preventing or ameliorating said neuromuscular disorder.
Embodiment 253 is a compound for use according to any one of the preceding embodiments, wherein said further active agent is an acetylcholine esterase inhibitor.
Embodiment 254 is a compound for use according to any one of the preceding embodiments, wherein said acetylcholine esterase inhibitor is selected from the group consisting of delta-9-tetrahydrocannabinol, carbamates, physostigmine, neostigmine, pyridostigmine, ambenonium, demecarium, rivastigmine, phenanthrene derivatives, galantamine, caffeine—noncompetitive, piperidines, donepezil, tacrine, edrophonium, huperzine, ladostigil, ungeremine and lactucopicrin.
Embodiment 255 is a compound for use according to any one of the preceding embodiments, wherein said acetylcholine esterase inhibitor is neostigmine or pyridostigmine.
Embodiment 256 is a compound for use according to any one of the preceding embodiments, wherein said further active agent is suggamadex.
Embodiment 257 is a compound for use according to any one of the preceding embodiments, wherein said further active agent is tirasemtiv.
Embodiment 258 is a compound for use according to any one of the preceding embodiments, wherein said further active agent is 3,4-aminopyridine.
Embodiment 259 is a method of treating, preventing and/or ameliorating a neuromuscular disorder, said method comprising administering a therapeutically effective amount of the compound as defined in any one of the preceding embodiments to a person in need thereof.
Embodiment 260 is a method of using a compound as defined in any one of the preceding embodiments, for the manufacture of a medicament for the treatment, prevention and/or amelioration of a neuromuscular disorder, and/or for reversing and/or ameliorating of a neuromuscular blockade.
Embodiment 261 is a method of reversing and/or ameliorating a neuromuscular blockade, said method comprising administering a therapeutically effective amount of the compound as defined in any one of the preceding embodiments to a person in need thereof.
Embodiment 262 is a method for recovery of neuromuscular transmission, said method comprising administering a therapeutically effective amount of the compound as defined in any one of the preceding embodiments to a person in need thereof.
Embodiment 262 is a method for recovering neuromuscular transmission, the method comprising administering a compound as defined in any one of the preceding embodiments to an individual in need thereof.
Compounds for testing were obtained from different suppliers including Enamine, Vitas, and CanAm Bioresearch. For synthesis of particular compounds please see below.
Compounds of formula (I) may be synthesized by the following synthetic strategies, general methods A-C:
1H-NMR spectra were recorded on a Bruker AM-300 spectrometer and were calibrated using residual nondeuterated solvent as internal reference. Spectra were processed using Spinworks version 4.0 (developed by Dr. Kirk Marat, Department of Chemistry, University of Manitoba).
The product was analysed by Waters 2695 HPLC consisting of a Waters 996 photodiode array detector, Kromasil Eternity C18, 5 μm, 4.6×150 mm column. Flow rate: 1 mL/minute, run time 20 minutes. Solvent A: methanol; solvent B: 0.1% formic acid in water. Gradient 0-100% Solvent B over 15 minutes with monitoring at 280 nm.
Waters Acquity UPLC, X-Select; column: Waters X-Select UPLC C18, 1.7 μm, 2.1×30 mm. Solvent A: 0.1% formic acid in water; solvent B: 0.1% formic acid in MeCN. Gradient 5-95% Solvent B over 10 minutes; detector: diode array.
All data are expressed as mean with SEM. Significant difference between groups was ascertained using a Students t-test (paired for contra-lateral muscles). Statistical analysis was performed using Sigmaplot 12.0 including fitting of data (
To a solution of starting compound, Ph3P, and ((R)-methyl 2-hydroxypropanoate in a solvent like DCM was added DEAD at 0° C. After stirring for 1 to 24 h at room temperature, the reaction completion was observed by NMR testing of a sample. Aqueous workup was performed. The compound was purified by chromatography.
To a solution of the product of Step A in ethanol was added an aqueous solution of an alkali like KOH. The resulting mixture was refluxed for 1-12 h, and reaction was monitored by TLC. At the end of reaction, the mixture was subjected to an aqueous/acidic work up using a solvent like DCM or an ether. The compound was purified by chromatography if necessary.
To a cold solution of pyridine in a solvent like DCM was added trifluoromethanesulfonic anhydride at below 0° C. After stirring for 5-60 min, (R)-methyl 2-hydroxypropanoate was added. The mixture was stirred for 1-10 h at room temperature, filtered, and the filtrate was partially evaporated.
To a mixture of 4-chloroaniline, a base like TEA and a solvent like DCM or DMF was added freshly prepared compound of step S at 0-5° C. The resulting mixture was stirred at 35° C. for 4 h, diluted with water, and extracted with DCM when the phases do not separate. Removal of the solvent yields the compound.
See Step C in Synthetic Method A above.
To a solution of acid amino acid in 1N H2SO4, a solution of NaNO2 in minimal quantity of water was added under cooling. The resulted mixture was stirred at room temperature for 1-3 days, saturated with Na2SO4, and extracted with a solvent like methyl-tert-butyl ether or DCM. The organic layer was evaporated.
To a suspension of NaH in DMF a solution of the product of step J in DMF was added. After stirring, p-fluoronitrobenzene or the desired electrophile was added and stirring continued at 100° C. for 3-48 h. The mixture was diluted a solution of NH4Cl and K2CO3 at room temperature, and extracted with a solvent like methyl-tert-butyl ether or ethyl acetate. The water layer was acidified with 3N HCl and extracted with methyl-tert-butyl ether or ethyl acetate. The organic layer was evaporated.
To a 0° C. solution of the product of step K in methanol, a catalytic amount of acetyl chloride was added. The mixture was heated under reflux for 3-9 h and the solvent was evaporated. The residue was extracted with a solvent like methyl-tert-butyl ether or DCM. The organic layer was evaporated.
To a solution of the product of step L in methanol, 10% Pd/C was added and hydrogenated under ambient pressure for 24 h. The mixture was filtered through silica gel and evaporated.
To a solution of t-BuNO2 in acetonitrile, CuBr2 was added. To the reaction mixture the product of step M in acetonitrile was added and the mixture was heated under reflux for 2-9 h. To the room temperature mixture, 20% aq. HCl was added and then extracted with a suitable solvent like methyl-tert-butyl ether or ethyl acetate. The organic layer was washed with water and evaporated. The oily residue was chromatographed.
See Step C in Synthetic Method A above.
The thioether obtained by Method A or B in a suitable solvent like DCM or ethyl acetate is treated with m-CPBA or another peracid at room temperature for 1-48 h and the reaction is monitored by TLC. After aqueous workup, the product is purified by chromatography.
See Step A in Synthetic Method A above.
See Step C in Synthetic Method A above.
The protected compound obtained from Step C in a suitable solvent like DCM is treated with TFA at room temperature for 1-18 h. After evaporation, the product is purified by reversed-phase chromatography with an HCl containing eluent.
The acid obtained by the previous methods in a suitable solvent like DCM or acetonitrile is treated DCC and the desired phenol, like p-nitrophenol, with a suitable catalyst like DMAP at room temperature for 1-48 h. After aqueous workup at acidic pH, the product is purified by rapid chromatography.
The ester obtained by the previous methods in a suitable solvent like toluene is treated DIBAL-H at −78° C. for 1 h. After aqueous workup, the product is purified by rapid chromatography.
The aldehyde obtained by the step F in a suitable solvent like DCM is treated at room temperature with the desired primary amine like 2-aminoethanol. Evaporation, redilution with DCM and re-evaporation yielded the desired product.
Method A involves the synthesis of compounds of Formula (X) (which is the same as Formula (I) in which R4 is H), which is an ether structure wherein Y=oxygen, and —R1, —R2, —R3 and —R4, are as defined in Formula (I) above. Compound (X), in the case where Y=O is a phenol, is available either commercially or synthetically (see below), and can be converted into an ether (XI) by methods which include Mitsunobu reaction conditions. This ether contains an ester functionality —CO2R11, which can be hydrolysed under a range of standard conditions, involving treatment with acid or base, to provide the carboxylic acid structure (XII), Y=O. Standard conditions for hydrolysis of the ester can also for example involve an enzymatic hydrolysis, employing for example an esterase or lipase. Furthermore, if an ester molecule (XI) comprises for example a (CH3)3SiCH2CH2O— group as —OR11, then a fluoride ion source such as tetra-n-butylammonium fluoride can be employed to convert (XI) into the corresponding carboxylic acid (XII).
Substituted phenols of general formula (X), Y=O, can be prepared by a variety of standard methods, for example by an ester rearrangement in the Fries rearrangement, by a rearrangement of N-phenylhydroxylamines in the Bamberger rearrangement, by hydrolysis of phenolic esters or ethers, by reduction of quinones, by replacement of an aromatic amine or by a hydroxyl group with water and sodium bisulfide in the Bucherer reaction. Other methods include hydrolysis of diazonium salts, by rearrangement reaction of dienones in the dienone phenol rearrangement, by the oxidation of aryl silanes or by the Hock process.
Carboxylic acids of Formula (X) (which is the same as Formula (I) in which R4 is H) can also be prepared by the procedure illustrated as General Method B. A phenolic ether of formula (XI) can be prepared by displacement of a suitable leaving group Q in (XIII) with the nucleophilic YH in (IX) (wherein Y=O). Q can for example be a halogen such as fluorine or iodine, and the ether product of formula (XI) can be converted into the carboxylic acid derivative (XII) by one of a range of methods outlined in General Method A, involving hydrolysis of the ester functionality.
Carboxylic acids of Formula (X) (which is the same as Formula (I) in which R4 is H) can be prepared by the procedure illustrated as General Method C. A phenolic ether of formula (XV) can be prepared by utilising e.g. Mitsunobu conditions when (X) is a phenol structure, i.e. Y=O, and (XIV) is a suitable secondary alcohol, i.e. Z=OH, and —R12 is a suitable protecting group, such as a silyl-containing moiety. On removal of the protecting group —R12, the primary alcohol in (XVI) can be oxidised to a carboxylic acid under standard conditions involving potassium permanganate, Jones oxidation conditions, the Heyns oxidation, ruthenium tetroxide or TEMPO, generating (XII).
To a solution of (R)-tert-butyl 2-hydroxypropanoate (1.2) (2.076 g, 14.20 mmol), 4-bromo-2-(isoxazol-5-yl)phenol (1.1) (3.75 g, 15.62 mmol) and triphenylphosphine (5.21 g, 19.88 mmol) in THF (150 mL) at 0° C. was added DIAD (3.87 mL, 19.88 mmol) dropwise over 20 min. The solution was stirred for a further 15 min at 0° C. The bright yellow solution was allowed to warm to RT and stirred overnight. MeOH (10 mL) was added and volatiles removed in vacuo to afford a dark orange oil. Formic acid (55 mL, 1434 mmol) was added and the mixture heated at 70° C. for 1 h. Volatiles were removed in vacuo and excess formic acid removed by co-evaporation with toluene (30 mL). Aq. NaOH (0.5 M) was added and the aqueous layer was washed with EtOAc (2×25 mL). The aqueous layer was acidified with aq. HCl (1 M) and extracted with EtOAc (3×25 mL). The combined organic extracts were dried over MgSO4 and adsorbed onto silica. The crude product was purified by chromatography on silica gel (80 g column, 0-100% EtOAc/isohexane) (eluting 40%) to afford (S)-2-(4-bromo-2-(isoxazol-5-yl)phenoxy)propanoic acid (1.3) (1.897 g, 5.77 mmol, 40.7% yield) as an off-white solid. The product was analysed by LCMS (Waters Acquity UPLC, C18, Waters X-Bridge UPLC C18, 1.7 μm, 2.1×30 mm, Acidic (0.1% Formic acid) 10 min method, 5-95% MeCN/water): 1923-89-B2, m/z 312.122 (M+H)+ (ES+); 310.072 (M−H)− (ES−), at 3.672 min, 100% purity @ 254 nm. 1H NMR (400 MHz, DMSO-d6) δ 13.29 (s, 1H); 8.70 (d, J=1.9 Hz, 1H); 7.98 (d, J=2.5 Hz, 1H); 7.64 (dd, J=8.9, 2.6 Hz, 1H); 7.16-7.02 (m, 2H); 5.16 (q, J=6.7 Hz, 1H); 1.61 (d, J=6.7 Hz, 3H).
To a solution of (S)-2-(4-bromo-2-(isoxazol-5-yl)phenoxy)propanoic acid (1.3) (1.017 g, 3.26 mmol) in MeCN (23 mL) was added NaHCO3 (0.274 g, 3.26 mmol) in H2O (8 mL) and the reaction stirred at room temperature for 30 min. After the alotted time, volatiles were removed in vacuo. Water was then added and the solution washed with CH2Cl2. The aqueous layer was then concentrated under reduced pressure and and excess formic acid removed by co-evaporation with toluene (30 mL). The resulting colourless solid was dried in a dessicator for 3 days. The product (1.4) was analysed by LCMS (Agilent Infinity, X-Select, Waters X-Select C18, 2.5 μm, 4.6×30 mm, Basic (0.1% Ammonium Bicarbonate) 4 min method, 5-95% MeCN/water): m/z 312.150 (M+H-Na)+ (ES+); 334.053, (M+H)+ (ES+); 312.061 (M−H)− (ES−), at 1.312 min, 100% purity @ 254 nm. 1H NMR (400 MHz, DMSO-d6) δ 8.66 (d, J=1.9 Hz, 1H); 7.90 (d, J=2.6 Hz, 1H); 7.52 (dd, J=9.0, 2.6 Hz, 1H); 7.21 (d, J=1.9 Hz, 1H); 6.95 (d, J=9.0 Hz, 1H); 4.47 (q, J=6.6 Hz, 1H); 1.47 (d, J=6.6 Hz, 3H).
Hydroxylamine hydrochloride (1.59 g, 22.88 mmol) was added to a stirred solution of 5-bromo-2-hydroxybenzaldehyde (2.1) (2.3 g, 11.44 mmol) and pyridine (2.78 ml, 34.3 mmol) in ethanol (20 ml) at room temperature. After 4 hours the mixture was diluted with water (200 ml), the solution was adjusted to pH 4-5 by addition of 1 M hydrochloric acid and stirred for 3 hours. The resulting precipitated solid was collected by filtration, washed with water (3×10 mL) and dried in vacuo at 45° C. for 3 days to afford (E)-5-bromo-2-hydroxybenzaldehyde oxime (2.2) (1.986 g, 9.14 mmol, 80% yield) as an off-white solid. The product was analysed by LCMS (Waters Acquity UPLC, X-Select, Waters X-Select UPLC C18, 1.7 μm, 2.1×30 mm, Acidic (0.1% Formic acid) 3 min method, 5-95% MeCN/water): m/z 216/218 (M+H)+ (ES+); at 1.268 min, 99.4% purity (diode array). 1H NMR (500 MHz, DMSO-d6) δ 11.48 (s, 1H), 10.31 (s, 1H), 8.27 (s, 1H), 7.65 (d, J=2.6 Hz, 1H), 7.37 (dd, J=8.7, 2.6 Hz, 1H), 6.86 (d, J=8.7 Hz, 1H).
N-Chlorosuccinimide (220 mg, 1.650 mmol) followed by 1 drop of 1 M hydrochloric acid were added to a stirred solution of (E)-5-bromo-2-hydroxybenzaldehyde oxime (2.2) (300 mg, 1.375 mmol) in DMF (6 mL) at room temperature. After 2 hours ethynylcyclopropane (0.140 mL, 1.650 mmol) was added followed by triethylamine (0.249 mL, 1.787 mmol) and the mixture maintained at room temp for 16 hours. Saturated sodium metabisulfite solution (2 ml) was added and the mixture was stirred for 10 min., then diluted with 0.5 M hydrochloric acid (30 ml) and extracted with ethyl acetate (30 ml). Organic extracts were washed with sodium bicarbonate solution (30 ml) then brine (10 ml), dried (MgSO4) and evaporated in vacuo. The residue was subjected to column chromatography (24 g Grace silica cartridge) eluting with a 0-100% ethyl acetate in isohexane gradient to afford 4-bromo-2-(5-cyclopropylisoxazol-3-yl)phenol (2.3) (172 mg, 0.522 mmol, 38.0% yield) as an oil. The product was analysed by LCMS (Waters Acquity UPLC, X-Select, Waters X-Select UPLC C18, 1.7 μm, 2.1×30 mm, Acidic (0.1% Formic acid) 3 min method, 5-95% MeCN/water) m/z 280/282 (M+H)+ (ES+); 278/280 (M−H)− (ES−), at 1.753 min, 85% purity (diode array). 1H NMR (500 MHz, DMSO-d6) δ 10.34 (s, 1H), 7.79 (d, J=2.6 Hz, 1H), 7.46 (dd, J=8.8, 2.6 Hz, 1H), 6.96 (d, J=8.8 Hz, 1H), 6.70 (s, 1H), 2.21 (qt, J=8.4, 5.0 Hz, 1H), 1.13-1.05 (m, 2H), 0.97-0.90 (m, 2H).
DIAD (0.163 mL, 0.840 mmol) was added to a stirred solution of 4-bromo-2-(5-cyclopropylisoxazol-3-yl)phenol (168 mg, 0.600 mmol), (R)-tert-butyl 2-hydroxypropanoate (96 mg, 0.660 mmol) and triphenylphosphine (220 mg, 0.840 mmol) in anhydrous THF (6 mL). After 2 hours reaction the solution was evaporated in vacuo to an oil. This oil was dissolved in formic acid (2 mL) and heated to 70° C. for 30 minutes. The mixture was evaporated in vacuo and the residue co-evaporated with toluene (4 ml). The residue was dissolved in ethyl acetate (30 mL) and extracted with 0.5 M sodium hydroxide solution (30 ml). The aqueous phase was washed with ethyl acetate (30 mL), acidified to pH 3-4 by dropwise addition of concentrated hydrochloric acid and extracted with ethyl acetate (30 mL). Organic extracts were dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography (12 g Grace silica cartridge) with 5-50% 99/1 ethyl acetate/acetic acid in isohexane gradient elution. Product-containing fractions were evaporated, the residue triturated with 4:1 isohexane/ethyl acetate (0.5 ml) and the solution decanted from the resulting solid which was washed with isohexane (0.5 ml) and dried overnight in vacuo at 45° C. to afford (S)-2-(4-bromo-2-(5-cyclopropylisoxazol-3-yl)phenoxy)propanoic acid (2.4) (96 mg, 0.271 mmol, 45% yield)
N-Chlorosuccinimide (360 mg, 2.69 mmol) followed by 1 drop of 1 M hydrochloric acid were added to a stirred solution of (E)-5-bromo-2-hydroxybenzaldehyde oxime (2.2) (485 mg, 2.245 mmol) in DMF (10 mL, 129 mmol). After 1 hour ethynyltrimethylsilane (0.311 mL, 2.245 mmol) and triethylamine (0.407 mL, 2.92 mmol) were added. After 16 hours, the mixture was diluted with water (50 mL), adjusted to pH 5-6 with 1M hydrochloric acid and extracted with ethyl acetate (50 ml). Organic extracts were washed with brine (25 ml), dried (MgSO4) and evaporated in vacuo. The residue was dissolved in dichloromethane (5 mL), the solution filtered then added to a 24 g silica cartridge equilibrated in isohexane. The column was eluted with 0-50% ethyl acetate in isohexane gradient to afford 4-bromo-2-(5-(trimethylsilyl)isoxazol-3-yl)phenol (3.1) (408 mg, 1.002 mmol, 44.6% yield) as an oil.
The product was analysed by LCMS (Waters Acquity UPLC, X-Select, Waters X-Select UPLC C18, 1.7 μm, 2.1×30 mm, Acidic (0.1% Formic acid) 3 min method, 5-95% MeCN/water): m/z 312/314 (M+H)+ (ES+); 310/312 (M−H)− (ES−), at 1.999 min, 76.7% purity (diode array). 1H NMR (500 MHz, DMSO-d6) δ 10.36 (s, 1H), 7.86 (d, J=2.6 Hz, 1H), 7.47 (dd, J=8.8, 2.6 Hz, 1H), 7.23 (s, 1H), 6.99 (d, J=8.8 Hz, 1H), 0.36 (s, 9H).
DIAD (266 mg, 1.314 mmol) was added to a stirred solution of 4-bromo-2-(5-(trimethylsilyl)isoxazol-3-yl)phenol (300 mg, 0.730 mmol), (R)-tert-butyl 2-hydroxypropanoate (149 mg, 1.022 mmol) and triphenylphosphine (345 mg, 1.314 mmol) in anhydrous tetrahydrofuran (6 ml, 0.730 mmol) at room temperature. After 2 hours the reaction mixture was evaporated in vacuo, the residue dissolved in 4:1 isohexane/dichloromethane and applied to a 24 g silica cartridge equilibrated in isohexane which was eluted with a 0-40% ethyl acetate in isohexane gradient to give (S)-tert-butyl 2-(4-bromo-2-(5 (trimethylsilyl)isoxazol-3-yl)phenoxy)propanoate (3.2) as an oil.
This oil was dissolved in formic acid (2 mL, 0.730 mmol) and heated to 70° C. for 2 hours. then evaporated and the residue co-evaporated with toluene (4 ml). The residue was dissolved in ethyl acetate (20 mL) and extracted with 0.5 M sodium hydroxide solution (20 ml). After 15 minutes the aqueous phases was acidified to pH 3-4, by dropwise addition of concentrated hydrochloric acid, and extracted with ethyl acetate (20 mL). Organic extracts were dried (MgSO4) and evaporated in vacuo. The residue was purified by column chromatography (12 g Grace silica cartridge) with 5-45% ethyl acetate/acetic acid (99/1) in isohexane gradient elution. Product-containing fractions were evaporated and the residue co-evaporated with toluene (4 mL). The residues was triturated with 4:1 isohexane/ethyl acetate (0.5 mL) and solvent decanted to give a solid product which was dried in vacuo at 45° C. overnight to afford (S)-2-(4-bromo-2-(isoxazol-3-yl)phenoxy)propanoic acid (3.3) (65 mg, 0.206 mmol, 28% yield).
Table B below illustrates Example compounds defined by the general Formula (I.3.4). In table B, the HPLC System is one of the methods as defined in the Materials and methods section.
1H NMR
1H NMR (500 MHz, DMSO-d6) δ
1H NMR (400 MHz, DMSO-d6) δ
Isolation of Muscles from Rats and Human, Ethical Approval, Dissection of Muscles, Solutions, and Chemicals
Experiments were performed using rat soleus muscles from either young (4-wk-old) or adult Wistar rats (12-14-week-old). Animal handling, killing and isolation of muscle is described elsewhere All experiments were performed using normal Krebs-Ringer bicarbonate solution (NKR). In solutions with elevated Mg2+, MgCl2 was added to NKR-solution causing minor increases in osmolarity and ionic strength. In solutions with elevated K+, 4 mM NaCl was replaced by 4 mM KCl in the NKR.
For experiments conducted using human abdominal muscle, details on patients, approval and the approaches for isolation, transportation, and experimentation are available elsewhere
In all contraction experiments, isometric force production was determined and force produced during contractions was quantified by measuring the integral of the force response (AUC). Stimulation and force recordings have been described elsewhere. Briefly, muscles were stimulated to contract in three different ways (
Isolated soleus muscles from adult rats or human abdominal muscles preparations were placed in a chamber and the resting membrane conductance (Gm) was measured in individual fibers using electrophysiological techniques described in detail elsewhere (
To measure endplate potentials (EPPs), soleus muscles from adult rats were placed in a chamber and the motor nerve was stimulated. To only measure EPPs, 1 μM of μ-conotoxin GiiiB was added to solution. All recordings were corrected for variation in resting membrane potential using −80 mV as the standard
The pharmacokinetic analysis of a single, intraperitoneal (I.P.) dose of C8 (10 mg/kg) was studied in young (4 weeks old) Sprague-Dawley rats. This part of the study was performed by Pipeline Biotech A/S (Spørring, Denmark). 24 animals were injected with C8 and three animals were sacrificed at times 15 min, 30 min, 1 hr, 2 hr, 4 hr, 6 hr, 8 hr, 24 hr after injection and plasma concentrations of C8 was determined using Liquid Chromatography Mass Spectrometry (LC-MS). Plasma concentrations (free and bound) were determined by OnTarget Chemistry (Uppsala, Sweden, Project No.: PB243-001).
Two sets of in vivo experiments were performed with C8: In the first series of experiments I.P. tubocurarine at (0.13 mg/kg) was used to induce a myasthenia like phenotype while in the second series of experiments a passive immunization model of myasthenia gravis was used in which rats were injected I.P. with a monoclonal antibody against the acetylcholine receptors at the neuromuscular endplate (MAB35, GTX14187, Genetex, 0.4-0.6 mg/kg). In both series of experiments, running performance was tested on a rotarod using a protocol where the rod was accelerated gradually over a 5 min period, and the running time and covered distance before falling off the rod were measured. To accustom the animals to the rotarod, the animals were tested three times on two consecutive days and animals that failed to complete the 5 min of running on the last day of familiarization period were not used in experiments. Experiments with tubocurarine were carried out over two days, and on each day the effect of tubocurarine on running performance was tested. On the first day only tubocurarine was injected. Animals that failed to respond to tubocurarine were not used on the next day of experimentation. On the second day, the animals were first allowed to run on the rotarod, and all animals performed normally. This shows that effects of the tubocurarine that had been injected on the day before had completely disappeared. Animals were then divided into two groups: One group was injected with 20 mg/kg C8 while the other group received sham treatment. 2 hrs after the C8 or sham injection, the second injection of tubocurarine was administered and the animals running performance on the rotarod was tested. The allocation of the animals into the two groups (C8 or sham) was random and unknown to the experimenter (blinded experimental design).
In experiments with MAB35, animals were first familiarized with the rotarod over two consecutive days and then injected I.P. with MAB35. After injection, rotarod performance was then again monitored regularly over the consecutive two days. Performance generally started to decline within 21-43 hrs after MAB35 injection, and if a stable reduction in performance was obtained, the animals were administered either C8 or sham. A considerable number of animals, however, became moribund failing to walk and they had altered ventilation (rapid) and pronounced ptosis. These animals were not included in experiments. Animals with a stable reduction in performance were injected with C8 (20 or 30 mg/kg) or sham treated and their performance were again monitored 2, 4, and 6 hrs after C8 or sham injection.
The aim was to find compounds that by inhibition of ClC-1 channels can recover nerve-stimulated force under conditions of fatigue including conditions where fatigue is caused by compromised neuromuscular transmission. Neuromuscular transmission dysfunction can develop because of both pre- and/or post-synaptic complications in connection with a disorder or as part of neuromuscular blockade during/after surgery. In the initial series of drug testing, experiments were performed with isolated muscles in the presence of sub-maximal ACh receptor antagonist tubocurarine. Since the inclusion of tubocurarine caused a partial loss of neuromuscular transmission this experiment mimics the conditions in myasthenia gravis and neuromuscular blockade. To mimic conditions with pre-synaptic complication (Lambert Eaton syndrome, motor neuron disorder, polyneuropathy) the intact nerve-muscle preparations were incubated at elevated extracellular Mg2+, which is known to suppress release of ACh from nerve terminals of motor neurons.
Experiments shown in
To initially confirm that inhibition of ClC-1 ion channels can be used to recover contractile force in muscle with reduced neuromuscular transmission, isolated nerve-muscle preparations were first exposed to either tubocurarine (
To identify ClC-1 inhibitors that could be used for treatment of neuromuscular disorders we repeated the experiment shown in
In a separate series of experiments with 8 isolated rat soleus muscles, ACh receptors were inhibited using 2 μM rocuronium, which is a clinically used neuromuscular blocking agent. Under these conditions the nerve-stimulated force was reduced to 51±5% of force before rocuronium. When 50 μM C8 was subsequently added nerve-stimulated contractile force was significantly recovered to 81±4% of force before rocuronium (p<0.01). This illustrates the potential of these compounds to be used as reversal agents.
The next series of experiments determined whether the compounds that recovered nerve-stimulated force in the presence of tubocurarine could also recover nerve-stimulated force at elevated extracellular Mg2+. To do this the experiment depicted in
The effect of compounds on ClC-1 ion channels was determined in muscle from adult rats using electrophysiological techniques described elsewhere. With this technique, three electrodes were placed in the same muscle fiber and by injecting small current pulses through two electrodes it was possible to obtain the voltage responses to this current injection at three inter-electrode distances. Examples of voltage responses at the three inter-electrode distances in a control fiber and in a fiber at 10 μM C8 are presented in
Also included are Kd values for compounds when tested in human muscle using an approach identical to that in rat muscle.
ClC-1 is a novel target in treatment of neuromuscular complications and it was therefore explored whether this approach for symptomatic treatment could be used in combination with existing symptomatic treatment approaches. In myasthenia gravis, which in isolated muscles was mimicked by tubocurarine, the symptoms of muscle fatigue are most commonly treated with inhibitors of acethylcholineesterase of which neostigmine and pyridostigmine are examples. Also, neostigmine is the most commonly used reversal agent of neuromuscular blocked after surgery. To test if ClC-1 inhibitors and neostigmine or pyridsostigmine can be used in combination, the concentration of tubocurarine that was required to depress nerve-stimulated force by 50% (Kd,tub) was determined in four experimental conditions: i) control conditions, ii) with ClC-1 inhibitor alone, iii) with neostigmine or pyridostigmine alone, and iv) with neostigmine or pyridostigmine and ClC-1 inhibitor together.
While the use of tubocurarine mimics conditions with reduced neuromuscular transmission due to post-synaptic dysfunction (myasthenia gravis, neuromuscular blockade), the experiments with elevated extracellular Mg2+ mimics conditions with pre-synaptic dysfunction akin to a range of neuromuscular disorders including Lambert Eaton syndrome, motor neuron disorders and polyneuropathy. Patients with Lambert Eaton syndrome are commonly treated with inhibitors of voltage gated K+ channels such as 3,4-diaminopyridine (3,4-AP). Based on this it was determined whether recovery of nerve-stimulated force at elevated extracellular Mg2+ with ClC-1 inhibiting compounds could be added to force recovery with 3,4-AP. This was done by determining the concentration of Mg2+ that was required to depress nerve-stimulated force by 50% (Kd,Mg2+) in four experimental conditions: i) in control conditions, ii) with 3,4-AP alone, iii) with C8 alone, and iv) with 3,4-AP and C8 together.
As illustrated in table 5, combination therapy using C8 and 3,4-diaminopyridine results in an unexpected synergistic effect on recovery of neuromuscular transmission.
Experiments with intracellular electrodes inserted near visible nerves in rat soleus muscles enabled recordings of EPPs upon nerve stimulation. To prevent action potential initiation upon nerve stimulation, μ-conotoxin GiiiB (1 μM) was included in the incubation solution to inhibit voltage gated Na+ channels in the muscle fibers (NaV1.4). As shown by representative recordings in
Critical illness myopathy (CIM) is a condition that develops in around 30% of critically ill patients in intensive care units. The condition is diagnosed from a loss of muscle excitability as evaluated from reduction in compound muscle action potentials. The associated muscle weakness prevents patients from weaning from mechanical ventilation and therefore increases the stay in intensive care units. At the cellular level, CIM is associated with loss of NaV1.4 function and muscle fibers become depolarized. To evaluate whether ClC-1 inhibition can recover muscle function in such conditions, depolarization and loss of NaV1.4 function in CIM were mimicked in experiments with isolated human muscles. Fibers were depolarized by raised extracellular K+, and loss of NaV1.4 function was induced by a small dose of NaV1.4 inhibitor TTX. As shown by
Before conducting in vivo experiments with animal models of myasthenia gravis, some pharmacokinetic details were obtained for C8 in response to one-bolus I.P. injection. The details from these experiments have been summarized in Table 6:
In the first series of in vivo experiments, myasthenia gravis was simply mimicked by I.P. injection of tubocurarine (0.13 mg/kg) in animals that had been familiarized to running on the rotarod. On the first of two consecutive days, tubocurarine was injected I.P. and the running performance of the animal was tested 21 minutes after this injection. On the second day of experimentation, the animals first performed a test run to ensure that they were no longer affected by the tubocurarine injected the day before. Then C8 (20 mg/kg) or sham treatment were injected I.P. and allowed to act for 2 hrs before again injecting tubocurarine. Animals were again tested 21 minutes after this second tubocurarine treatment. This experimental design enabled a paired analysis of whether the sham or C8 injections on the second day changed the response of the animals to tubocurarine. It should also be noted that the experimenter did not know which animals had been given C8 or sham treatment. The design of the experiments has been illustrated in
In the last series of experiments, myasthenia gravis was mimicked in rats by inducing an immunological reaction against the motor endplate of muscle fibers using monoclonal antibody against the nicotinic ACh receptor in muscle fibers. Again the animals had been familiarized to the rotarod before the MAB35 injection. As shown in
The investigatory goal of these experiments was to evaluate whether compounds inhibit ClC-1 channels in native tissue of rat skeletal muscle fibres. Apparent ClC-1 affinity was reported by the concentration of compound at which 50% of the compound's full inhibition of ClC-1 was observed (EC50).
ClC-1 Cl− ion channels generate around 80% of the total membrane conductance (Gm) in resting skeletal muscle fibres of most animals including rat and human. Other ion channels that contribute to Gm can therefore be considered negligible, and it is possible to evaluate whether a compound inhibits ClC-1 in rat muscle by comparing Gm measurements before and after exposure to a compound. ClC-1 inhibition would in such recordings be reflected by a reduction of Gm.
Experimentally, Gm was measured in individual fibres of whole rat soleus muscles using a three micro-electrodes technique described in this example and in full detail elsewhere. Briefly, intact rat soleus muscles were dissected out from 12-14 week old Wistar rats and placed in an experimental chamber that was perfused with a standard Krebs Ringer solution containing 122 mM NaCl, 25 mM NaHCO3, 2.8 mM KCl, 1.2 mM KH2PO4, 1.2 mM MgSO4, 1.3 mM CaCl2, 5.0 mM D-glucose. During experiments, the solution was kept at approx. 30° C. and continuously equilibrated with a mixture of 95% O2 and 5% CO2, pH˜7.4. The experimental chamber was placed in Nikon upright microscope that was used to visualize individual muscle fibres and the three electrodes (glass pipettes filled with 2 M potassium citrate). For Gm measurements, the electrodes were inserted into the same fibre with known inter-electrode distances of 0.35-0.5 mm (V1-V2, X1) and 1.1-1.5 mm (V1-V3, X3) (
To establish a dose response relationship, Gm was first determined in 10 muscle fibres in the absence of compound and then at four increasing compound concentrations with Gm determinations in 5-10 fibres at each concentration. The average Gm values at each concentration were plotted against compound concentration and the data was fitted to sigmoidal function to obtain an EC50 value (
In conclusion, this example demonstrates that the compounds of the present invention have an EC50 value in the range of 1-12 μM.
The current invention relates to compounds that inhibit ClC-1 ion channels and increase muscle excitability and thereby improve muscle function in clinical conditions where muscle activation is failing. Such conditions result in loss of contractile function of skeletal muscle, weakness and excessive fatigue. In this series of experiments the compounds were tested for their ability to restore contractile function of isolated rat muscle when the neuromuscular transmission had been compromised akin to neuromuscular disorders.
Experimentally, soleus muscles from 4-5 wk old rats were isolated with the motor nerve remaining attached. The nerve-muscle preparations were mounted in experimental setups that enabled electrical stimulation of the motor nerve. Stimulation of the motor nerve led to activation of the muscle fibres and ensuing force production that was recorded. The nerve-muscle preparations were also in these experiments incubated in the standard Krebs Ringer (see example) and the solution was heated to 30° C. and continuously equilibrated with a mixture of 95% O2 and 5% CO2, pH˜7.4.
After mounting the nerve-muscle preparation in the experimental setup, the contractile function of the muscle was initially assessed under the control conditions (
In conclusion, this example demonstrates that the compounds of the present invention are able to increase muscle excitability and thereby improve muscle function in clinical conditions. The muscle contractility was recovered by 15-40% points, which meant almost complete restoration of the force.
