Patent Application
20050085553
The present invention relates to an agent for treating mild cognitive impairment.
Mild cognitive impairment (MCI) is also referred as mild memory impairment. Patients with MCI are diagnosed as neither normal nor dementia, and their cognitive abilities are at the level between normal and dementia. Generally, patients with MCI have mild memory deficit, mild cognitive deficit, and minimal dysfunction in activities of daily living. According to a recent report, mild cognitive impairment could be regarded as the initial stage of or a transitional phase to Alzheimer's disease (AD) because the conditions of MCI patients steadily progressed to more severe stages of dementia and in many cases, pathological observations in their nerves were similar to those of AD patients (Archive of Neurology, vol.58, pp.397-405 (2001)).
Alzheimer's disease is a neurodegenerative disorder characterized by senile plaque formation and neurofibrillary tangles as well as nerve cell degeneration and loss. The most characteristic feature of Alzheimer's disease is senile plaques, which are formed by deposition of biological constituents in the brain, whose principal component is β-amyloid protein (hereafter, may be simply referred as Aβ) (Biochemical Biophysical Research Communication, vol.122, pp.1131 (1984)). It is known that Aβ consists of 40 or 42 amino acids (hereafter, simply referred as Aβ40 or Aβ42, respectively) and has a cytotoxic effect on nerve cells (Trend in Neuroscience (TINS), vol.16, pp.409 (1993); Science, vol.274, pp.99 (1996); Nature, vol.395, pp.755 (1998); Neurobiology of Aging, vol.201, pp.20 (1999), etc.).
Thus, drugs for inhibiting production or secretion of Aβ are effective in preventing or treating Alzheimer's disease. An enzyme immunoassay (EIA) technique for Aβ has been established recently, which enables not only screening of compounds inhibiting the secretion of Aβ from neuronal cell culture but also determination of the quantities of Aβ in various biological tissues, blood and cerebrospinal fluid (for example, Science, vol; 264, pp.1336 (1994); Biochemistry, vol.34, pp.10272 (1995); Science, vol.274, pp.99 (1996)).
The precursor protein of Aβ, APP (Amyloid Precursor Protein) is cleaved by the action of β-secretase and γ-secretase to produce Aβ. Some laboratories have reported recently that cDNA of β-secretase was isolated and then identified (for example, Science, vol.286, pp.735 (1999); Nature, vol.402, pp.533 (1999); Nature, vol.402, pp.537 (1999)). It was found that some familial Alzheimer's disease patients have mutation in the APP gene and it was reported that the cells transfected with the mutant genes increased Aβ production and secretion (for example, Nature, vol.360, pp.672 (1992), Science, vol.259, pp.514 (1993); Science, vol.264, pp.1336 (1994)). Accordingly, it is considered that drugs for inhibiting β-secretase can inhibit Aβ production or secretion and therefore are useful for preventing or treating patients who have increased Aβ protein in their brains, such as those who are susceptible to diseases caused by Aβ genetically (for example, Alzheimer's disease and Down's syndrome), in particular, familial Alzheimer's disease, and those who have increased Aβ protein in their brains due to trauma or the like.
Moreover, inhibition of β-secretase leads to blocking or inhibiting a metabolic pathway from APP to Aβ protein, while it leads to accelerating secretion of secretory APP that is produced by the action of α-secretase (hereafter, simply referred as sAPPα). It has been reported that sAPPα has a neurotrophic factor-like activity (Neuron, vol.10, pp.243-254 (1993); Trend in Neuroscience (TINS), vol.16, pp.409 (1993), etc.). Such a neurotrophic factor-like activity includes (1) a nerve cell-survival or -maintenance, (2) an accelerating activity on formation of synapses, (3) a preventing activity on nerve cells death and (4) a long-term potentiation on nerve cells in hippocampus. Thus it is considered that drugs for inhibiting β-secretase can accelerate secretion of sAPPα and therefore are useful for preventing or treating (1) neurodegenerative disease, (2) nervous disorder due to cerebrovascular injury, head trauma, spinal cord injury, sequelae of encephalitis, or cerebral palsy, (3) memory impairment, (4) mental disease, and the like.
However, it has never been demonstrated that active treatment of mild cognitive impairment with recognition that mild cognitive impairment is a kind of disease may inhibit development of Alzheimer's disease.
On the other hand, JP-A 11-80098 discloses an amyloid β-protein production or secretion inhibitor which comprises a compound represented by the formula:
wherein, Ar is an optionally substituted aromatic group, X is (i) a bond, (ii) —S—, —SO— or —SO2—, (iii) C1-6 alkylene, C2-6 alkenylene or C2-6 alkynylene, each of which may be substituted with one to three substituents selected from oxo and C1-6 alkyl, (iv) —CO—O— or (v) a group represented by the formula: —(CH2)p-X1—, —(CH2)p-X1—(CH2)q-, —(CH2)r-CO—X1—, —SO2—NR8—, or —(CH2)r-SO2—NR8—, wherein X1 is an oxygen atom or NR8, R8 is a hydrogen atom, an optionally substituted hydrocarbon group or acyl, p is an integer of 0 to 5, q is an integer of 1 to 5, p+q is an integer of 1 to 5, and r is an integer of 1 to 4; Y is a divalent C1-6 aliphatic hydrocarbon group in which an oxygen atom or a sulfur atom may intervene and which may be substituted, R1 and R2 are independently a hydrogen atom or an optionally substituted lower alkyl, or R1 and R2 are taken together with the adjacent nitrogen atom to form an optionally substituted nitrogen-containing heterocyclic ring, ring A is a benzene ring which may be further substituted in addition to the group represented by the formula —X—Ar wherein each symbol is as defined above; and ring B is a 4- to 8-membered ring which may be further substituted in addition to the group represented by the formula —Y—NR1R2 wherein each symbol is as defined above; or a salt thereof.
JP-A 8-502587 (WO94/10569) discloses a method for identifying a β-amyloid peptide (βAP) production inhibitor.
JP-A 7-165606 discloses a method for identifying a βAP production inhibitor.
JP-A 10-509797 (WO96/15452) discloses a method for detecting a soluble β-amyloid peptide in a liquid sample.
JP-A 11-507538 (WO96/40885) discloses a composition comprising isolated and purified enzymes which specifically cleave β-amyloid precursor protein at the β-amyloid peptide cleavage sites.
JP-A 9-178743 discloses a method for determining the quantity of soluble β-amyloid precursor protein (APP) by using an antibody against β-amyloid protein or soluble APP.
The present invention is intended to provide an agent for treatment of mild cognitive impairment and to inhibit the progression of mild cognitive impairment to Alzheimer's disease.
The present inventors made their efforts at establishing treatment of mild cognitive impairment and as a result, found that compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein are useful for treating mild cognitive impairment and inhibiting the progression of MCI to Alzheimer's disease, and finally completed the present invention.
Namely, the present invention provides:
The term “mild cognitive impairment”, as used herein, means impairment whose clinical condition is on a level of 0.5 according to clinical dementia rating (CDR: subjects are assessed for six categories such as memory, orientation, judgment and the like using 5-stage rating, 0 (normal) to 3 (severe), and based on the result, the final score is calculated using a given algorithm) described in Neurology, vol.43, pp.2412-2414, 1993 (see mentioned-above Archive of Neurology, vol.58. pp.397-405 (2001)).
The compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein used in the present invention include compounds having an inhibitory effect on β-secretase, compounds having an inhibitory effect on γ-secretase and compounds having an inhibitory effect on accumulation of γprotein.
The compounds having an inhibitory effect on secretase include compounds represented by the above mentioned formula (I) (hereafter, simply referred as compound (I)), or salts or prodrugs thereof.
In the compound (I), Ar indicates an optionally substituted aromatic group.
The “aromatic group” of the “optionally substituted aromatic group” represented by Ar includes a monocyclic aromatic group, a ring-assembly aromatic group and a fused aromatic group.
The “monocyclic aromatic group” includes a monovalent group which is formed by removing any one of hydrogen atoms from a benzene ring or a 5- or 6-membered aromatic heterocycle.
The “5- or 6-membered aromatic heterocycle” includes a 5- or 6-membered aromatic heterocycle containing one or more (for example, 1 to 3 and preferably 1 or 2) heteroatoms selected from a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms. Specific examples thereof are thiophene, furan, pyrrole, imidazole, pyrazole, thiazole, oxazole, pyridine, pyrazine, pyrimidine, pyridazine ring and the like.
Specific examples of the monocyclic aromatic group mentioned above include phenyl, 2- or 3-thienyl, 2- or 3-furyl, 1-, 2- or 3-pyrrolyl, 2- or 4-imidazolyl, 3- or 4-pyrazolyl, 2-, 4- or 5-thiazolyl, 2-, 4- or 5-oxazolyl, 2-, 3- or 4-pyridyl, 2-pyrazinyl, 2-, 4- or 5-pyrimidinyl, and 3- or 4-pyridazinyl and in particular, phenyl is preferable among them.
The “ring-assembly aromatic group” includes a group formed by removing any one of hydrogen atoms from an aromatic ring assembly in which two or more (preferably, 2 or 3) aromatic rings are directly bound through single bonds and in which the number of the single bonds through which the rings are directly bound is one less than the number of the rings. The “aromatic ring” includes aromatic hydrocarbon and an aromatic heterocycle.
The “aromatic hydrocarbon” includes C6-14 monocyclic or fused polycyclic (for example, dicyclic or tricyclic) aromatic hydrocarbon (for example, benzene, naphthalene, indene, or anthracene).
The “aromatic heterocycle” include 5- to 14-membered, preferably 5- to 10-membered aromatic heterocycles containing one or more (for example, one to four and preferably, one to two) heteroatoms selected form a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms. Specific examples thereof include aromatic heterocycles such as thiophene, benzothiophene, benzofuran, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphtho[2,3-b]thiophene, furan, phenoxathiin, pyrrole, imidazole, pyrazole, oxazole, isoxazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole, pyridine, pyrazine, pyrimidine, pyridazine, indole, isoindole, 1H-indazole, purine, 4H-quinolizine, isoquinoline, quinoline, phthalazine, naphthylidine, quinoxaline, quinazoline, cinnoline, carbazole, β-carboline, phenanthridine, acridine, phenazine, thiazole, isothiazole, phenothiazine, furazan, phenoxazine, phthalimide, 2-, 3- or 4-pyridone, or 2-, 3- or 4-quinolone, and fused rings of the above mentioned aromatic heterocycle (preferably monocycle) with one or more (preferably, one or two) aromatic rings (for example, a benzene ring).
As the aromatic ring assembly in which aromatic rings are directly bound through single bonds, for example, an aromatic ring assembly consisting of two or three (preferably, two) rings selected from a benzene ring, a naphthalene ring and 5- to 10-membered (preferably, 5- or 6-membered) aromatic heterocycles may be used. Preferable examples of the aromatic ring assembly include an aromatic ring assembly consisting of two or three aromatic rings selected from benzene, naphthalene, pyridine, pyrimidine, thiophene, furan, thiazole, isothiazole, oxazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole, quinoline, isoquinoline, indole, benzothiophene, benzoxazole, benzothiazole and benzofuran. More specific examples thereof include 2-, 3- or 4-biphenylyl, 3-(1-naphthyl)-1,2,4-oxadiazol-5-yl, 3-(2-naphthyl)-1,2,4-oxadiazol-5-yl, 3-(2-benzofuranyl)-1,2,4-oxadiazol-5-yl, 3-phenyl-1,2,4-oxadiazol-5-yl, 3-(2-benzoxazolyl)-1,2,4-oxadiazol-2-yl, 3-(3-indolyl)-1,2,4-oxadiazol-2-yl, 3-(2-indolyl)-1,2,4-oxadiazol-2-yl, 4-phenylthiazol-2-yl, 4-(2-benzofuranyl)thiazol-2-yl, 4-phenyl-1,3-oxazol-5-yl, 5-phenylisothiazol-4-yl, 5-phenyloxazol-2-yl, 4-(2-thienyl)phenyl, 4-(3-thienyl)phenyl, 3-(3-pyridyl)phenyl, 4-(3-pyridyl)phenyl, 6-phenyl-3-pyridyl, 5-phenyl-1,3,4-oxadiazol-2-yl, 4-(2-naphthyl)phenyl, 4-(2-benzofuranyl)phenyl and 4,4′-terphenyl, and among them, biphenylyl(2-, 3- or 4-biphenylyl) is preferable.
The “fused aromatic group” includes a monovalent group formed by removing any one of hydrogen atoms from a fused polycyclic (preferably, dicyclic to tetracyclic and preferably, dicyclic or tricyclic) aromatic ring. The “fused polycyclic aromatic ring” includes a fused polycyclic aromatic hydrocarbon and a fused polycyclic aromatic heterocycle.
The “fused polycyclic aromatic hydrocarbon” includes a fused polycyclic (dicyclic or tricyclic) aromatic C9-14 hydrocarbon (for example, naphthalene, indene, anthracene).
The “fused polycyclic aromatic heterocycle” includes a 9- to 14-membered, preferably 9- or 10-membered fused polycyclic aromatic heterocycle containing one or more (for example, one to four) heteroatoms selected from a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms. Specific examples thereof include aromatic heterocycles such as benzofuran, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphtho[2,3-b]thiophene, isoquinoline, quinoline, indole, quinoxaline, phenanthridine, phenothiazine, phenoxazine and phthalimide.
Specific examples of the above-mentioned fused aromatic group include 1-naphthyl, 2-naphthyl, 2-quinolyl, 3-quinolyl, 4-quinolyl, 2-benzofuranyl, 2-benzothiazolyl, 2-benzimidazolyl, 1-indolyl, 2-indolyl and 3-indolyl, and among them, 1-naphthyl and 2-naphthyl are preferable.
A substituent for the aromatic group represented by Ar includes halogen atoms (for example, fluorine, chlorine, bromine, or iodine), C1-3 alkylenedioxy (for example, methylenedioxy or ethylenedioxy), nitro, cyano, optionally halogenated C1-6 alkyl, C6-10 aryloxy-C1-6 alkyl (for example, phenoxymethyl), C1-6 alkyl-C6-10 aryl-C2-6 alkenyl (for example, methylphenylethenyl), optionally halogenated C3-6 cycloalkyl, optionally substituted C7-16 aralkyl, optionally halogenated C1-6 alkoxy, optionally halogenated C1-6 alkylthio, hydroxy, optionally substituted C6-10 aryloxy, C6-10 aryl-C7-16 aralkyloxy (for example, phenylbenzyloxy), amino, mono-C1-6 alkylamino (for example, methylamino, ethylamino, propylamino, isopropylamino, or butylamino), di-C1-6 alkylamino (for example, dimethylamino, diethylamino, dipropylamino, dibutylamino, or ethylmethylamino), optionally substituted 5- to 7-membered saturated cyclic amino, acyl, acylamino and acyloxy. Said “aromatic group” may have, for example, one to five (preferably, one to three) of the above-mentioned substituents at the substitutable positions, and if it has two or more substituents, the substituents may be the same or different from each other.
The “C7-16 aralkyl” of the “optionally substituted C7-16 aralkyl” among the above mentioned substituents for the aromatic groups represented by Ar, includes benzyl, phenethyl and naphthylmethyl.
The “C6-10 aryloxy” of the “optionally substituted C6-10 aryloxy” includes phenyloxy and naphthyloxy. A “substituent” for these “optionally substituted C7-16 aralkyl” and “optionally substituted C6-10 aryloxy” includes halogen atoms (for example, fluorine, chlorine, bromine, or iodine), C1-3 alkylenedioxy (for example, methylenedioxy or ethylenedioxy), nitro, cyano, optionally halogenated C1-6 alkyl, optionally halogenated C3-6 cycloalkyl, optionally halogenated C1-6 alkoxy, optionally halogenated C1-6 alkylthio, hydroxy, amino, mono-C1-6 alkylamino (for example, methylamino, ethylamino, propylamino, isopropylamino, or butylamino), di-C1-6 alkylamino (for example, dimethylamino, diethylamino, dipropylamino, dibutylamino, or ethylamino), formyl, carboxy, carbamoyl, optionally halogenated C1-6 alkyl-carbonyl, C1-6 alkoxy-carbonyl (for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, or tert-butoxycarbonyl), mono-C1-6 alkyl-carbamoyl (for example, methylcarbamoyl, or ethylcarbamoyl), di-C1-6 alkyl-carbamoyl (for example, dimethylcarbamoyl, diethylcarbamoyl, or ethylmethylcarbamoyl), optionally halogenated C1-6 alkylsulfonyl, formylamino, optionally halogenated C1-6 alkyl-carboxamido, C1-6 alkoxy-carboxamido (for example, methoxycarboxamido, ethoxycarboxamido, propoxycarboxamido, or butoxycarboxamido), C1-6 alkylsulfonylamino (for example, methylsulfonylamino, or ethylsulfonylamino), C1-6 alkyl-carbonyloxy (for example, acetoxy, or propanoyloxy), C1-6 alkoxy-carbonyloxy (for example, methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, or butoxycarbonyloxy), mono-C1-6 alkyl-carbamoyloxy (for example, methylcarbamoyloxy or ethylcarbamoyloxy), and di-C1-6 alkyl-carbamoyloxy (for example, dimethylcarbamoyloxy or diethylcarbamoyloxy), and one to five of these substituents may be used.
The “5- to 7-membered saturated cyclic amino” of the “optionally substituted 5- to 7-membered saturated cyclic amino” among the above mentioned substituents for the aromatic groups represented by Ar, includes morpholino, thiomorpholino, piperazin-1-yl, piperidino, pyrrolidin-1-yl and hexamethylen-1-yl. A “substituent” for the “optionally substituted 5- or 7-membered saturated cyclic amino” includes optionally halogenated C1-6 alkyl, optionally substituted C6-14 aryl, optionally substituted C7-19 aralkyl, optionally substituted 5- to 10-membered aromatic heterocyclic groups, optionally substituted C6-10 aryl-carbonyl, optionally halogenated C1-6 alkyl-carbonyl and optionally halogenated C1-6 alkylsulfonyl, and one to three of these substituents may be used.
Here, the “C6-14 aryl” of the “optionally substituted C6-14 aryl” includes phenyl, 1-naphthyl, 2-naphthyl, 2-indenyl and 2-anthryl. Among them phenyl is preferable. The “C7-19 aralkyl” of the “optionally substituted C7-19 aralkyl” includes benzyl, phenethyl, diphenylmethyl, triphenylmethyl, 1-naphthylmethyl, 2-naphthylmethyl, 2,2-diphenylethyl, 3-phenylpropyl, 4-phenylbutyl and 5-phenylpentyl, and benzyl is preferable among them. The “5-to 10-membered aromatic heterocyclic group” of the “optionally substituted 5- to 10-membered aromatic heterocyclic group” includes 2-, 3- or 4-pyridyl, 1-, 2- or 3-indolyl and 2- or 3-thienyl, and 2-, 3- or 4-pyridyl is preferable among them. The “C6-10 aryl-carbonyl” of the “optionally substituted C6-10 aryl-carbonyl” includes benzoyl, 1-naphthoyl and 2-naphthoyl. A “substituent” for these “optionally substituted C6-14 aryl”, “optionally substituted C7-19 aralkyl”, “optionally substituted 5- to 10-membered aromatic heterocyclic group” and “optionally substituted C6-10 aryl-carbonyl” respectively include halogen atoms (for example, fluorine, chlorine, bromine, or iodine), C1-3 alkylenedioxy (for example, methylenedioxy, or ethylenedioxy), nitro, cyano, optionally halogenated C1-6 alkyl, optionally halogenated C3-6 cycloalkyl, optionally halogenated C1-6 alkoxy, optionally halogenated C1-6 alkylthio, hydroxyl, amino, mono-C1-6 alkylamino (for example, methylamino, ethylamino, propylamino, isopropylamino, or butylamino), di-C1-6 alkylamino (for example, dimethylamino, diethylamino, dipropylamino, dibutylamino, or ethylmethylamino), formyl, carboxy, carbamoyl, optionally halogenated C1-6 alkyl-carbonyl, C1-6 alkoxy-carbonyl (for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, or tert-butoxycarbonyl), mono-C1-6 alkyl-carbamoyl (for example, methylcarbamoyl or ethylcarbamoyl), di-C1-6 alkyl-carbamoyl (for example, dimethylcarbamoyl, diethylcarbamoyl, or ethylmethylcarbamoyl), optionally halogenated C1-6 alkylsulfonyl, formylamino, optionally halogenated C1-6 alkyl-carboxamido, C1-6 alkoxy-carboxamido (for example, methoxycarboxamido, ethoxycarboxamido, propoxycarboxamido, or butoxycarboxamido), C1-6 alkylsulfonylamino (for example, methylsulfonylamino or ethylsulfonylamino), C1-6 alkyl-carbonyloxy (for example, acetoxy or propanoyloxy), C1-6 alkoxy-carbonyloxy (for example, methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, or butoxycarbonyloxy), mono-C1-6 alkyl-carbamoyloxy (for example, methylcarbamoyloxy or ethylcarbamoyloxy), and di-C1-6 alkylcarbamoyloxy (for example, dimethylcarbamoyloxy or diethylcarbamoyloxy), and one to five of these substituents may be used.
In the “acyl”, “acylamino” and “acyloxy” exemplified above as the “substituent” for the “optionally substituted aromatic group” represented by Ar, “acyl” includes acyl groups represented by the formula: —CO—Ra —CO—ORa, —CO—NRaRa, —CS—NHRa, —SO2—Raa, or SO—Raa
wherein, Ra is (i) a hydrogen atom,
Examples of the “optionally substituted 5- to 7-membered saturated cyclic amino” exemplified as a substituent for Ra and Raa are the same as those mentioned above.
The hydrocarbon groups represented by Ra and Raa include groups formed by removing one hydrogen atom from a hydrocarbon compound, and may be, for example, chain or cyclic hydrocarbon groups (for example, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, or aralkyl). Among them, the following C1-19 chain or cyclic hydrocarbon groups are preferable:
The heterocyclic groups represented by Ra and Raa include monovalent groups formed by removing any one hydrogen atom from a 5- to 14-membered (monocyclic, dicyclic, or tricyclic) heterocyclic ring containing one to four (preferably, one to three) of one or two kinds of heteroatoms selected from a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms, preferably (i) a 5- to 14-membered (preferably, 5- to 10-membered) aromatic heterocyclic ring, (ii) a 5- to 10-membered nonaromatic heterocyclic ring or (iii) a 7- to 10-membered bridged heterocyclic ring.
The “5- to 14-membered (preferably, 5- to 10-membered) aromatic heterocyclic ring” mentioned above includes aromatic heterocycles such as thiophene, benzothiophene, benzofuran, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphtho[2,3-b]thiophene, furan, phenoxathiin, pyrrole, imidazole, pyrazole, oxazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole, pyridine, pyrazine, pyrimidine, pyridazine, indole, isoindole, 1H-indazole, purine, 4H-quinolizine, isoquinoline, quinoline, phthalazine, naphthyridine, quinoxaline, quinazoline, cinnoline, carbazole, β-carboline, phenanthridine, acridine, phenazine, thiazole, isothiazole, phenothiazine, isoxazole, furazan, phenoxazine or phthalimide, and fused rings of the above-mentioned aromatic heterocycle (preferably monocycles) with one or more (preferably, one or two) aromatic rings (for example, a benzene ring).
The “5- to 10-membered nonaromatic heterocyclic ring” mentioned above includes pyrrolidine, imidazoline, pyrazolidine, pyrazoline, piperidine, piperazine, morpholine and thiomorpholine.
The “7- to 10-membered bridged heterocyclic ring” mentioned above includes quinuclidine and 7-azabicyclo[2.2.1]heptane.
The “heterocyclic group” is preferably a 5- to 10-membered (monocyclic or bicyclic) heterocyclic group containing one to four of one or two kinds of heteroatoms selected from a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms. Specific examples thereof include aromatic heterocyclic groups such as 2- or 3-thienyl, 2-, 3- or 4-pyridyl, 2- or 3-furyl, 2-, 3-, 4-, 5- or 8-quinolyl, 4-isoquinolyl, pyrazinyl, 2- or 4-pyrimidinyl, 3-pyrrolyl, 2-imidazolyl, 3-pyridazinyl, 3-isothiazolyl, 3-isoxazolyl, 1-indolyl, 2-indolyl and 2-isoindolinyl, and nonaromatic heterocyclic groups such as 1-, 2- or 3-pyrrolidinyl, 2- or 4-imidazolinyl, 2-, 3- or 4-pyrazolidinyl, piperidino, 2-, 3- or 4-piperidyl, 1- or 2-piperazinyl and morpholino. Among them, for example, a 5- or 6-membered heterocyclic group containing one to three hetero atoms selected from a nitrogen atom, a sulfur atom and an oxygen atom in addition to carbon atoms is preferable, and specifically, 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-furyl, 3-furyl, pyrazinyl, 2-pyrimidinyl, 3-pyrrolyl, 3-pyridazinyl, 3-isothiazolyl, 3-isoxazolyl, 1-, 2- or 3-pyrrolidinyl, 2- or 4-imidazolinyl, 2-, 3- or 4-pyrazolidinyl, piperidino, 2-, 3- or 4-piperidyl, 1- or 2-piperazinyl, or morpholino is used.
The “C1-6 alkyl” represented by Rb includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl and hexyl.
The “nitrogen-containing heterocyclic ring” which Ra and Rb together with the adjacent nitrogen atom form includes a 5- to 7-membered nitrogen-containing heterocyclic ring which contains at least one nitrogen atom and may contain one to three heteroatoms selected from a nitrogen atom, a sulfur atom and an oxygen atom, in addition to carbon atoms, for example, piperidine, morpholine, thiomorpholine, piperazine and pyrrolidine.
Preferable examples of the “acyl” exemplified as a “substituent” for the “aromatic group” represented by Ar include formyl, carboxy, carbamoyl, optionally halogenated C1-6 alkyl-carbonyl, C1-6 alkoxy-carbony, (for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, or tert-butoxycarbonyl), optionally substituted C6-10 aryl-carbonyl, optionally substituted C6-10 aryloxy-carbonyl, optionally substituted C7-16 aralkyloxy-carbonyl, optionally substituted 5- to 6-membered heterocyclic carbonyl, mono-C1-6 alkyl-carbamoyl, di-C1-6 alkyl-carbamoyl (for example, dimethylcarbamoyl, diethylcarbamoyl, or ethylmethylcarbamoyl), optionally substituted C6-10 aryl-carbamoyl, optionally substituted 5- to 6-membered heterocyclic carbamoyl, optionally halogenated C1-6 alkylsulfonyl, and optionally substituted C6-10 arylsulfonyl.
Among them, the “C6-10 aryl-carbonyl” of the “optionally substituted C6-10 aryl-carbonyl” includes benzoyl, 1-naphthoyl and 2-naphthoyl. The “C6-10 aryloxy-carbonyl” of the “optionally substituted C6-10 aryloxy-carbonyl” includes phenoxycarbonyl. The “C7-16 aralkyloxy-carbonyl” of the “optionally substituted C7-16 aralkyloxy-carbonyl” includes benzyloxycarbonyl and phenethyloxycarbonyl. The “5- to 6-membered heterocyclic carbonyl” of the “optionally substituted 5- to 6-membered heterocyclic carbonyl” includes nicotinoyl, isonicotinoyl, 2-thenoyl, 3-thenoyl, 2-furoyl, 3-furoyl, morpholinocarbonyl, piperidinocarbonyl and 1-pyrrolidinylcarbonyl. The “C6-10 aryl-carbamoyl” of the “optionally substituted C6-10 aryl-carbamoyl” includes phenylcarbamoyl, 1-naphthylcarbamoyl and 2-naphthylcarbamoyl. The “5- to 6-membered heterocyclic carbamoyl” of the “optionally substituted 5- to 6-membered heterocyclic carbamoyl” includes 2-pyridylcarbamoyl, 3-pyridylcarbamoyl, 4-pyridylcarbamoyl, 2-thienylcarbamoyl, and 3-thienylcarbamoyl. The “C6-10 arylsulfonyl” of the “optionally substituted C6-10 arylsulfonyl” includes benzensulfonyl, 1-naphthalenesulfonyl and 2-naphthalelesulfonyl.
A “substituent” for these “optionally substituted C6-10 arylcarbonyl”, “optionally substituted C6-10 aryloxy-carbonyl”, “optionally substituted C7-16 aralkyloxy-carbonyl”, “optionally substituted 5- to 6-membered heterocyclic carbonyl”, “optionally substituted C6-10 aryl-carbamoyl”, “optionally substituted 5- to 6-membered heterocyclic carbamoyl” and “optionally substituted C6-10 arylsulfonyl” includes halogen atoms, C1-3 alkylenedioxy, nitro, cyano, optionally halogenated C1-6 alkyl, optionally halogenated C1-6 alkoxy, optionally halogenated C1-6 alkylthio, hydroxy, amino, mono-C1-6 alkylamino, di-C1-6 alkylamino, formyl, carboxy, carbamoyl, optionally halogenated C1-6 alkyl-carbonyl, C1-6 alkoxy-carbonyl, mono-C1-6 alkyl-carbamoyl, di-C1-6 alkyl-carbamoyl, optionally halogenated C1-6 alkylsulfonyl, formylamino, optionally halogenated C1-6 alkyl-carboxamido, C1-6 alkoxy-carboxamido, C1-6 alkylsulfonylamino, C1-6 alkyl-carbonyloxy, C1-6 alkoxy-carbonyloxy, mono-C1-6 alkyl-carbamoyloxy and di-C1-6 alkyl-carbamoyloxy, and one to five, preferably one to three of these substituents may be used.
The “acylamino” exemplified as a “substituent” for the “optionally substituted aromatic group” represented by Ar mentioned above includes mono- or di-substituted amino with the “acyl” described in detail in the explanation of a “substituent” for the “optionally substituted aromatic group” represented by Ar mentioned above, and preferably, acylamino represented by the following formula:
—NRc—CORd, —NRc—COORda, —NRc—SO2RRda, or —NRc—CONRdaRdb
wherein, Rc is a hydrogen atom or C1-6 alkyl, Rd has the same meaning as that of Ra mentioned above, Rda has the same meaning as that of Raa mentioned above, and Rdb has the same meaning as that of Rb.
The “C1-6 alkyl” represented by Rc and Rdb includes similar groups to “C1-6 alkyl” represented by Rb.
The “acylamino” exemplified as a “substituent” for the “optionally substituted aromatic group” represented by Ar includes preferably formylamino, optionally halogenated C1-6 alkyl-carboxamido, optionally substituted C6-10 aryl-carboxamido (for example, phenylcarboxamido or naphthylcarboxamido), C1-6 alkoxy-carboxamido (for example, methoxycarboxamido, ethoxycarboxamido, propoxycarboxamido, or butoxycarboxamido), and C1-6 alkylsulfonylamino (for example, methylsulfonylamino or ethylsulfonylamino).
The “acyloxy” exemplified as a “substituent” for the “optionally substituted aromatic group” represented by Ar mentioned above includes mono-substituted oxy with the “acyl” described in detail in the explanation of a “substituent” for the “optionally substituted aromatic group” represented by Ar mentioned above, and preferably, acyloxy represented by the following formula:
—O—CORe, —O—COORe, or —O—CONHRe
wherein, Re has the same meaning as that of Ra mentioned above.
The “acyloxy” exemplified as a “substituent” for the “optionally substituted aromatic group” represented by Ar includes preferably, C1-6 alkyl-carbonyloxy (for example, acetoxy or propanoyloxy), optionally substituted C6-10 aryl-carbonyloxy (for example, benzoyloxy, 1-naphthoyloxy, or 2-naphthoyloxy), C1-6 alkoxy-carbonyloxy (for example, methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, or butoxycarbonyloxy), mono-C1-6 alkyl-carbamoyloxy (for example, methylcarbamoyloxy or ethylcarbamoyloxy), di-C1-6 alkyl-carbamoyloxy (for example, dimethylcarbamoyloxy or diethylcarbamoyloxy), optionally substituted C6-10 aryl-carbamoyloxy (for example, phenylcarbamoyloxy or naphthylcarbamoyloxy) and nicotinoyloxy. A “substituent” for these “optionally substituted C6-10 aryl-carboxamido”, “optionally substituted C6-10 aryl-carbonyloxy” and “optionally substituted C6-10 aryl-carbamoyloxy” and “preferable example” thereof include similar groups to the “substituent” for the “optionally substituted C6-10 aryl-carbonyl” mentioned above.
Among the above mention, preferably Ar may represent an optionally substituted ring-assembly aromatic group (in particular, biphenylyl such as 2-, 3- or 4-biphenylyl).
In the compound (I), X is a divalent C1-6 aliphatic hydrocarbon group which may contain one or two divalent groups selected from —O—, —S—, —CO—, —SO—, —SO2— and —COO— and Y is a divalent C1-6 aliphatic hydrocarbon group.
Said C1-6 aliphatic hydrocarbon group includes C1-6 alkylene, C2-6 alkenylene and C2-6 alkynylene.
Said C1-6 alkylene includes C1-3 alkylene (for example, —CH2—, —(CH2)2—, or —(CH2)3—) which may contain one to three C1-3 alkyl, as well as straight-chain C1-6 alkylene such as —CH2—, —(CH2)2—, —(CH2)3—, —(CH2)4—, —(CH2)5— and —(CH2)6—.
Said C2-6 alkenylene includes C2-3 alkenylene (for example, —CH≡CH— or —CH2—CH≡CH—) which may have one to three C1-3 alkyl, as well as straight-chain C2-6 alkenylene such as —CH═CH— and —CH2—CH═CH—.
Said C2-6 alkynylene includes C2-3 alkynylene (for example, —C≡C—, —CH2—C≡C—, —C≡C—CH2—, —C≡C—CH2CH2—, or —CH2CH2—C≡C—) which may have one to three C1-3 alkyl, as well as straight-chain. C2-6 alkynylene such as —C≡C—, —CH2—C≡C—, —C≡C—CH2—, —C≡C—CH2CH2—, —CH2CH2—C≡C—, —CH2—C≡C—CH2—, —(CH2)2—C≡C—CH2—, —(CH2)2—C≡C—(CH2)2—, and —(CH2)3—C≡C—CH2—.
Said C1-6 aliphatic hydrocarbon group may be preferably a C1-3 aliphatic hydrocarbon group such as C1-3 alkylene, C2-3 alkenylene and C2-6 alkynylene.
In particular, preferably, X is C1-3 alkylene containing one —O— and Y is C1-3 alkylene.
In the compound (I), R1 and R2 may be the same or different and each indicates optionally substituted C1-6 alkyl.
The “C1-6 alkyl” of the “optionally substituted C1-6 alkyl” represented by R1 and R2 includes methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl and hexyl, and among them, methyl, ethyl and propyl are preferable.
A “substituent” for the “optionally substituted C1-6 alkyl” represented by R′ or R″ includes halogen atoms (for example, fluorine, chlorine, bromine, or iodine), C1-3 alkylenedioxy (for example, methylenedioxy or ethylenedioxy), nitro, cyano, optionally halogenated C1-6 alkyl, optionally halogenated C3-6 cycloalkyl, optionally halogenated C1-6 alkoxy, optionally halogenated C1-6 alkylthio, hydroxy, amino, mono-C1-6 alkylamino (for example, methylamino, ethylamino, propylamino, isopropylamino or butylamino), di-C1-6 alkylamino (for example, dimethylamino, diethylamino, dipropylamino, dibutylamino, or ethylmethylamino), formyl, carboxy, carbamoyl, optionally halogenated C1-6 alkyl-carbonyl, C1-6 alkoxy-carbonyl (for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, or tert-butoxycarbonyl), mono-C1-6 alkyl-carbamoyl (for example, methylcarbamoyl or ethylcarbamoyl), di-C1-6 alkyl-carbamoyl (for example, dimethylcarbamoyl, diethylcarbamoyl or diethylmethylcarbamoyl), optionally halogenated C1-6 alkylsulfonyl, formylamino, optionally halogenated C1-6 alkyl-carboxamido, C1-6 alkoxy-carboxamido (for example, methoxycarboxamido, ethoxycarboxamido, propoxycarboxamido, or butoxycarboxamido), C1-6 alkylsulfonylamino (for example, methylsulfonylamino or ethylsulfonylamino), C1-6 alkyl-carbonyloxy (for example, acetoxy or propanoyloxy), C1-6 alkoxy-carbonyloxy (for example, methoxycarbonyloxy, ethoxycarbonyloxy, propoxycarbonyloxy, or butoxycarbonyloxy), mono-C1-6 alkyl-carbamoyloxy (for example, methylcarbamoyloxy or ethylcarbamoyloxy), di-C1-6 alkyl-carbamoyloxy (for example, dimethylcarbamoyloxy or diethylcarbamoyloxy) and optionally substituted aromatic groups, and one to five, preferably one to three of these substituents may be used. If the number of substituents is two or more, the individual substituents may be either the same or different from each other.
In the compound (I), ring A indicates a benzene ring which may have an additional substituent. Namely, the ring A may have an additional substituent in addition to the group represented by the formula Ar—X— at the substitutable position. Such a substituent includes halogen atoms (for example, fluorine, chlorine, bromine, or iodine), optionally halogenated C1-6 alkyl, optionally halogenated C1-6 alkoxy, hydroxy and amino. The “optionally halogenated C1-6 alkyl” and “optionally halogenated C1-6 alkoxy” include similar groups to the “optionally halogenated C1-6 alkyl” and “optionally halogenated C1-6 alkoxy” described in detail in the explanation of Ar mentioned above, respectively. A substituent for the ring A includes, preferably, halogen atoms (for example, chlorine) and C1-6 alkoxy (for example, methoxy). The ring A may be substituted with one to three of such substituents at the substitutable positions, and if it has two or more substituents, each substituent may be the same or different. In particular, the ring A is preferably substituted with the only substituent represented by the formula Ar—X—.
In the compound (I), ring B indicates a 4- to 8-membered ring which may have an additional substituent.
The 4- to 8-membered ring represented by the ring B includes a 4- to 8-membered homocyclic or heterocyclic ring which may have one double bond in addition to the site fused with the ring A and may have one to three heteroatoms selected from an oxygen atom, a nitrogen atom and a sulfur atom in addition to carbon atoms. A specific example thereof includes a ring represented by the following formula:
wherein,
is a single or double bond, and
Said “4- to 8-membered ring” includes, preferably, a ring represented by the following formula:
wherein, Z has the same meaning as that mentioned above. Preferably, such a ring is a 6-membered homocyclic or heterocyclic ring which does not contain a double bond other than the site fused with the ring A and may contain one oxygen atom or imino in addition to carbon atoms.
The “substituent” for the “4- to 8-membered ring which may have an additional substituent” represented by the ring B includes oxo, C1-6 alkyl (for example, methyl, ethyl, propyl, isopropyl, or butyl) and hydroxy. Such a ring may be substituted with one to three of these substituents at the substitutable positions and if it has two or more substituents, the individual substituents may be either the same or different from each other.
The ring B is preferably a 6-membered homocyclic or heterocyclic ring which does not have a substituent other than the group represented by the following formula:
The fused ring of the ring A and the ring B includes preferably rings represented by the following formula:
Among them, tetralin is preferable.
The compound (I) includes, in particular, 6-(4-biphenylyl) methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin (also referred as 6-[(1,1′-biphenyl)-4-ylmethoxy]-1,2,3,4-tetrahydro-N,N′-dimethyl-2-naphtaleneethanamine), 6-(4-biphenylyl)methoxy-2-(N,N-dimethylamino)methyltetralin, 6-(4-biphenylyl)methoxy-2-(N,N-dipropylamino)methyltetralin, 2-(N,N-dimethylamino)methyl-6-(4′-methoxybiphenyl-4-yl)methoxytetralin, 6-(4-biphenylyl)methoxy-2-[2-(N,N-diethylamino)ethyl]tetralin, 2-[2-(N,N-dimethylamino)ethyl]-6-(4′-methylbiphenyl-4-yl)methoxytetralin, 2-[2-(N,N-dimethylamino)ethyl]-6-(4′-methoxybiphenyl-4-yl)methoxytetralin, 6-(2′,4′-dimethoxybiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin, 6-[4-(1,3-benzodioxol-5-yl)phenyl]methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin, and 6-(3′,4′-dimethoxybiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin, and optically active forms and hydrates thereof. Among them, preferred are (R)-(+)-6-(4-biphenylyl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin (also referred as (R)-6-[(1,1′-biphenyl)-4-ylmethoxy]-1,2,3,4-tetrahydro-N,N-dimethyl-2-naphtaleneethanamine)hydrochloride monohydrate (compound A), (+)-6-(4-biphenylyl)methoxy-2-[2-(N,N-diethylamino)ethyl]tetralin, (+)-2-[2-(N,N-dimethylamino)ethyl]-6-(4′-methylbiphenyl-4-yl)methoxytetralin, (+)-2-[2-(N,N-dimethylamino)ethyl]-6-(4′-methoxybiphenyl-4-yl)methoxytetralin, (+)-6-(2′,4′-dimethoxybiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin, (+)-6-[4-(1,3-benzodioxol-5-yl)phenyl]methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin, and (+)-6-(3′,4′-dimethoxybiphenyl-4-yl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin.
The compound (I) can be produced according to the method disclosed in JP-A 11-80098 (WO98/38156) or WO01/74756. Alternatively, if an amide bond and an ether bond are present in the same molecule, the compound may be produced by an improved method wherein only the ether bond is selectively broken in the presence of methanesulfonic acid and methionine and then alkylation reaction is undergone to reduce the amide moiety.
Another compound having an inhibitory activity on β-secretase which may be used in the present invention is, for example, OM99-2 (Science, 290, 150-153; J. Am. Chem. Soc., 2000, 122, 3522-3523) represented by the following formula:
Compounds having an inhibitory activity on γ-secretase which may be used in the present invention include L-685458 represented by the following formula:
LY-374973 (Investigation Drugs, db, 2001.1) represented by the following formula:
and RF-978 represented by the following formula:
Compounds having an inhibitory activity on aggregation of β protein which may be used in the present invention include PTI-00703, ALZHEMED (NC-531), PPI-368 represented by the following formula:
and PPI-558(WO98/08868), SKF-74652 represented by the following formula:
Salts of compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein include salts with inorganic bases, ammonium salts, salts with organic bases, salts with inorganic acids, salts with organic acids, and salts with basic or acidic amino acids.
Preferable examples of salts with inorganic bases include alkali metal salts such as a sodium salt and a potassium salt; alkali earth metal salts such as a calcium salt, a magnesium salt and a barium salt; and a aluminum salt. Preferable examples of salts with organic bases include salts with trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, triethanolamine, dicyclohexylamine or N,N-dibenzylethylenediamine. Preferable examples of salts with inorganic acids include salts with hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid or phosphoric acid. Preferable examples of salts with organic acids include salts with formic acid, acetic acid, trifluoroacetic acid, fumaric acid, oxalic acid, tartaric acid, maleic acid, citric acid, succinic acid, malic acid, methanesulfonic acid, benzenesulfonic acid, or p-toluenesulfonic acid. Preferable examples of salts with basic amino acids include salts with arginine, lysine or ornithine and preferable examples of salts with acidic amino acids include salts with aspartic acid or glutamic acid.
Among these salts, pharmacologically acceptable salts are preferred. For example, if the compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein contains an acidic functional group, an inorganic salt such as an alkali metal salt (for example, a sodium salt or a potassium salt) or an alkali earth metal salt (for example, a calcium salt, a magnesium salt, or a barium salt) or an ammonium salt is used. If the compound contains a basic functional group, an inorganic salt such as hydrochloride, sulfate, phosphate or hydrobromate or an organic salt such as acetate, maleate, fumarate, succinate, methanesulfonate, p-toluenesulfonate, citrate or tartrate is used. In the case of the compound (I), among them, hydrochloride, citrate and fumarate are preferable.
Moreover, the compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein may be anhydrous or hydrous. If being hydrous, the compound may contain one to three H2O molecules.
The compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein which may be used in the present invention, for example, the compound (I) may be in the stereoisomeric form depending on the kind of substituents which the compound has, and the single stereoisomer or a mixture of the stereoisomers may be used in the present invention.
Moreover, if the compound (I) exists as a configurational isomer, diastereomer, conformer or the like, if desired, the isomers may be separated according to a known method for separating and purifying them. In addition, if the compound (I) is racemic, it may be separated into d-form and 1-form using a standard optical resolution technique. In the present invention, though these separated isomers or a mixture of these isomers may be used, use of optically active substances is more suitable in many cases.
The compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein may be a prodrug thereof. Said prodrug means a compound which is converted into a compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein by a reaction with an enzyme, gastric acid or the like under the in vivo physiological condition, namely (1) a compound which is converted into the desired compound by enzymatic oxidation, reduction, hydrolysis or the like or (2) a compound which is converted into the desired compound by hydrolysis or the like with gastric acid. The prodrug of the compound having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein includes a compound whose hydroxyl group is acylated, alkylated, phosphorylated or borated or a salt thereof (for example, a compound whose hydroxyl group is acetylated, palmitoylated, propanoylated, pivaloylated, succinylated, fumarylated, alanylated or dimethylaminomethylcarbonylated or a salt thereof) and a compound whose carboxyl group is esterified or amidated (for example, compound whose carboxyl group is ethylesterified, phenylesterified, carboxyoxymethylesterified, dimethylaminomethylesterified, pivaloyloxymethylesterified, ethoxycarbonyloxyethylesterified, phthalidylesterified, (5 -methyl-2-oxo-1,3-dioxolen-4-yl)methylestrified, cyclohexyloxycarbonylethylesterified or methylamidated, or a salt thereof). These prodrugs can be produced according to any method known per se or its modification.
Alternatively, prodrugs of the compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein may be converted into the compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein under the physiological condition described in “Development of Medical Drugs” (Hirokawashoten, vol.7 Molecular design, pp.163-198, 1990).
The compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein may be labeled with an isotope (for example, 2H, 3H, 14C, 35S, or 125I) or the like.
The above-mentioned compounds having an inhibitory effect on production, secretion, aggregation and/or accumulation of. β-amyloid protein (including a salt thereof) or a prodrug thereof (hereafter, simply referred as the β-amyloid protein-inhibiting compound) is useful in treating mild cognitive impairment because of its inhibitory effect on production, secretion, aggregation and/or accumulation of β-amyloid protein.
The β-amyloid protein inhibiting compounds may be used in treating mild cognitive impairment in combination with, for example, therapeutic drugs of Alzheimer's disease (for example, cholinesterase inhibitors such as donepezil, rivastigmine, galantamine and TAK-147, or brain function activators such as idebenone, memantine and vinpocetine), antiparkinson drugs (for example, L-dopa, deprenyl, carbidopa+levodopa, pergolide, ropinirol, cabergoline, pramipexole, entacapone, or lazabemide), amyotrophic lateral sclerosis therapeutic drugs (for example, riluzole, mecasermin, or gabapentin), neurotrophic factors, antidepressants (for example, fluoxetine, sertraline, paroxetine, venlafaxine, nefazodone, reboxetine, imipramine hydrochloride, or duloxetine), schizophrenia therapeutic drugs (for example, olanzapine, risperidone, questiapine, or iloperidone), antianxiety drugs (for example, alprazolam, bromazepam, chlordiazepoxide, diazepam, etizolam, flutoprazepam, or lorazepam), sleeping drugs (for example, brotizolam, estazolam, flurazepam, nitrazepam, or triazolam), antihyperlipemic drugs (for example, simvastatin, fluvastatin, pravastatin, or atrovastatin), antihypertensive drugs (for example, captopril, delapril, enalapril, nifedipine, nicardipine, amlodipine, alprenolol, propranolol, metroprolol, losartan, valsartan, or candesartan), antiplatelet drugs (for example, ticlopidine, heparin, urokinase, alteplase, tisokinase, nasaruplase or cilostazol), antioxidants (for example, linolenic acid, ascorbic acid, icosapentaenoic acid, docosahexaenoic acid, or tocopherol), vitamins (for example, tocopherol or ascorbic acid), sex hormones (for example, estrogen, estrone, or estradiol), antiinflammatory drugs (for example, predonisolone, betamethasone, or dexamethasone), nonsteroidal antiinflammatory drugs (for example, indomethacin, ibuprofen, acetylsalicylic acid, diclofenac, naproxen, or piroxicam), COX-2 inhibitors (for example, celecoxib or rofecoxib), drugs for improving brain circulation and metabolism (for example, nicergoline, ibudilast, or ifenprodil), anticonvulsants (for example, carbamazepin, valproic acid, clonazepam, vigabatrin, lamotrigine or gabapentin) or pnarmacologically acceptable salts thereof.
The β-amyloid protein inhibiting compound used in the present invention, in particular the compound (I), in combination with the above-mentioned drug, can be also effectively used for prevention or treatment of not only mild cognitive impairment, but also neurodegenerative diseases (for example, senile dementia, Alzheimer's disease, Down's disease, Parkinson's disease, Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, or diabetic neuropathy), cerebrovascular disorders (for example, brain circulation disorder associated with cerebral infarction, intracerebral hemorrhage or cerebral arteriosclerosis), nervous disorders associated with head injury/spinal cord injury, sequelae of encephalitis or cerebral palsy, memory deficit (for example, senile dementia or amnesia) or mental diseases (for example, depression, panic disorder or schizophrenia).
The β-amyloid protein inhibiting compound, in particular compound (I), or a salt or prodrug thereof is low toxic and may be efficiently delivered into the brain.
Accordingly, the β-amyloid protein inhibiting compound including the compound (I) is useful as a safe therapeutic agent for mild cognitive impairment in mammals (for example, rats, mice, guinea pigs, rabbits, sheeps, horses, pigs, cattle, monkeys, or human beings).
The therapeutic agent for mild cognitive impairment of the present invention can be produced by formulation of the above mentioned β-amyloid protein inhibiting compound according to any method known per se. The β-amyloid protein inhibiting compound may be administered safely and orally or parenterally (for example, locally, rectally, or intravenously) as it is or as a pharmaceutical composition, for example, a tablet (including a sugar-coated tablet and a film-coated tablet), a granule, a capsule (including a soft capsule), liquid, injection, a suppository, or a sustained-release agent, which is prepared by mixing with an appropriate quantity of a pharmacologically acceptable carrier in the formulation process.
The content of the β-amyloid protein inhibiting compound in the therapeutic agent for mild cognitive impairment of the present invention can be selected appropriately depending on the efficacy of the compound and the like. For example, the content of the compound (I) is usually about 0.1 to 100% by weight of the total agent. The dosage of the agent of the present invention depends on a subject to be administered, an administration route, disease to be treated, and the like. For example, when the agent of the present invention is orally administered to an adult patient (about 60 kg) with Alzheimer's disease, the daily dose is about 0.01 to 500 mg, preferably about 0.1 to 100 mg, more preferably 1 to 100 mg based on the active component (compound (I)), which may be administered in one to several portions per day.
A pharmacologically acceptable carrier used in production of the therapeutic agent for mild cognitive impairment of the present invention includes various organic or inorganic carriers which are conventionally used as formulation materials, for example, excipients, lubricants, binders and disintegrants for solid preparations; and solvents, solubilizing agents, suspending agents, isotonizing agents, buffers or soothing agents for liquid preparations. In addition, additives may be used if necessary, including antiseptics, antioxidants, coloring agents, sweetening agents, absorbing agents and wetting agents.
Excipients include lactose, white sugar, D-mannitol, starch, cornstarch, crystalline cellulose and light anhydrous silicic acid.
Lubricants include magnesium stearate, calcium stearate, talc and colloidal silica.
Binders include crystalline cellulose, white sugar, D-mannitol, dextrin, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, polyvinylpyrrolidone, starch, sucrose, gelatin, methyl cellulose and carboxymethyl cellulose sodium.
Disintegrants include starch, carboxymethyl cellulose, carboxymethyl cellulose calcium, croscarmellose sodium, carboxymethyl starch sodium and L-hydroxypropyl cellulose.
Solvents include water for injection, alcohol, propylene glycol, macrogol, sesame oil and corn oil.
Solubilizing agents include polyethylene glycol, propylene glycol, D-mannitol, benzyl benzoate, ethanol, tris-aminomethane, cholesterol, triethanolamine, sodium carbonate and sodium citrate.
Suspending agents include surfactants such as stearyltriethanolamine, sodium lauryl sulfate, laurylamino propionic acid, lecithin, benzalkonium chloride, benzethonium chloride and glyceryl monostearate; and hydrophilic polymers such as polyvinyl alcohol, polyvinylpyrrolidone, carboxymethyl cellulose sodium, methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose and hydroxypropyl cellulose.
Isotonizing agents include glucose, D-sorbitol, sodium chloride, glycerin and D-mannitol.
Buffers include buffer solutions of phosphate, acetate, carbonate and citrate.
Soothing agents include benzyl alcohol.
Antiseptics include p-hydroxybenzoic esters, chlorobutanol, benzyl alcohol, phenethyl alcohol, dehydroacetic acid and sorbic acid.
Antioxidants include sulfite salt, ascorbic acid and sodium ascorbate.
For stability in the presence of light or the like, the agent of the present invention may be also coated with a light-blocking coating according to a conventional method. As the coating base, for example, hydroxypropylmethyl cellulose, ethyl cellulose, hydroxymethyl cellulose or the like may be used. To the base, titanium dioxide, iron sesquioxide or the like may be added. As a plasticizer for a film, for example, polyethylene glycol may be further added. In the case of the agent comprising the compound (I), copolyvidone is suitably used as a plasticizer.
Heireinbelow, with reference to Referential Examples, Examples and Experimental Examples concerning the compound (I), the present invention is described in detail but is not limited to the compound and applicable to other compounds.
695 g of (+)-N,N-dimethyl-(6-(4-biphenylyl)methoxy-2-tetralin)acetamide (obtained in accordance with the method disclosed in JP-A 11-310561) was suspended in 3475 mL of a toluene solution. To the suspension, 562 g of sodium dihydro-bis(2-methoxyethoxy)aluminate (a 70% solution in toluene) was added dropwise at an internal temperature of 20° C. or below under a nitrogen atmosphere. After stirring at room temperature for 1.5 hours, 695 mL of an aqueous 4N sodium hydroxide solution was added dropwise at 20° C. or below. The mixture was stirred at room temperature for 30 minutes and then separated. An organic layer was washed twice with 695 mL of an aqueous 1N sodium hydroxide solution and twice with 1390 mL of water. To the organic layer added was 348 mL of toluene, and the mixture was heated up to 60° C. and 175 mL of concentrated hydrochloric acid (content: 36%) was added dropwise thereto. After stirring for an hour under ice-cooling, a precipitated crystal was filtered and washed with 695 mL of toluene and 1390 mL of an aqueous 50% methanol solution. The crystal was dried under reduced pressure at 40° C. to obtain 723 g (yield: 94.4%) of the titled compound as a pale yellow crystal.
1H-NMR (300 MHz, DMSO-d6) δ: 1.32-1.40(1H, m), 1.62-1.74(3H, m), 1.82-1.90(1H, m), 2.28-2.38(1H, m), 2.74(6H, s), 2.76-2.82(3H, br), 3.08-3.16(2H, m), 5.09(2H, s), 6.72-6.80(2H, m), 6.96(1H, d, J=8.0 Hz), 7.32-7.38(1H, m), 7.44-7.54(4H, m), 7.64-7.72(4H, m), 10.4(1H, br).
479.8 g of (R)-(+)-6-(4-biphenylyl)methoxy-2-[2-(N,N-dimethylamino)ethyl]tetralin hydrochloride monohydrate obtained in the Referential Example 1 was dissolved in a mixture of 3186 mL of tetrahydrofuran and 864 mL of water at 60° C. To the solution 24 g of activated carbon was added and the mixture was stirred at 60° C. for 30 minutes. The activated carbon was filtered out and washed with a mixture of 336 mL of tetrahydrofuran and 216 mL of water. The filtrate was heated up to 60° C. and 2688 mL of tetrahydrofuran was added dropwise thereto while being stirring. After the mixture was cooled to room temperature and further stirred at 5 to 10° C. for 2 hours, a precipitated crystal was separated by a centrifuge method. The separated crystal was washed with a mixture of 216 mL of tetrahydrofuran and 744 mL of water to obtain the pure titled compound (390.5 g, 85%).
A therapeutic agent for mild cognitive impairment of the present invention was produced in accordance with the formulation shown in Table 1.
2.3 g of compound A, 222.2 g of lactose and 50 g of cornstarch were mixed homogeneously in a fluidized-bed granulation dryer. In the dryer, the mixture was sprayed with an aqueous solution containing 9 g of hydroxypropyl cellulose, granulated and then dried. The resulting granules were crushed with a 1.5 mmφ punching screen of a power mill to obtain sized powder. To 226.8 g of the sized powder, 12 g of croscarmellose sodium and 1.2 g of magnesium stearate were added and mixed to obtain granules for tableting. The granules were compressed into plain tablets (one tablet weight: 150 mg) with a 7.5 mmφ mallet in a tableting machine. The resulting plain tablets were sprayed with a solution of hydroxypropylmethyl cellulose 2910 and copolyvidone in which titanium dioxide and iron sesquioxide were dispersed in a film coating machine to obtain about 1500 film-coated tablets which contain 1.15 mg of compound A per one tablet as shown in Table 1. Similarly, a 5 mg tablet and a 50 mg tablet were produced.
An Ameliorative Effect of the Agent on Learning Deficit in Old Rats
1) Method
Fisher344 rats (27-month old, male) were previously subjected to four trials of a water maze test using a pool with a diameter of 90 cm and a platform on the surface of water in the pool. The rats with remarkable disability to swim were excluded and the rest were divided into several groups. The compound A (0.3 or 1.0 mg/kg) was orally administered to the rats once a day for 14 days. On the 10th day, the rats were subjected to four trials of a water maze test using a platform on the surface of water in a pool and confirmed again that they had no difficulty in swimming ability. Starting from the next day, the rats were subjected four times a day for 3 days to a water maze test using a pool with a diameter of 120 cm and a platform submerged below the surface of water in the pool. In this test, the time required for the rats to arrive at the platform was measured. Two trials were expressed as one block. During the behavioral pharmacological test period, the drug was administered after the test.
2) Results
The results are shown in
An Effect on Increase in Insoluble Aβ40/42 and Amyloid Plaque Formation in the Brains of Transgenic Mice with Swedish APP Mutation
1) Method
Transgenic mice with Swedish amyloid precursor protein (APP) mutation (7- to 8-month old) were given solid feed containing the compound A (56 ppm) (equivalent to a dosage of about 7 mg/kg/day) or control feed for six months. After six months from the administration, one cerebral hemisphere was used for brain histological examination and the other hemisphere was used for determining the quantity of Aβ40/42. Cerebral cortex was used for measuring the quantity of Aβ. The accumulation type of insoluble Aβ40/42 protein were extracted by homogenization of the cerebral cortex in 25 times amount of Tris buffer (containing a protease inhibitor) followed by centrifugation to remove the supernatant. Then, 19 times amount of 70% formic acid was added to the insoluble precipitation and homogenized to solubilize it. After centrifugation, the supernatant was diluted to 1/20 with 1M Tris solution for neutralization and the diluted supernatant was used for determining the quantity of Aβ40/42 contained therein. Using enzyme-linked immunosorbent assay (ELISA), the quantity of accumulation-type Aβ40/42 was measured.
For histopathological search, two sections containing dorsal hippocampus were prepared from each mouse and then immunostained for Aβ40/42 with BAN50 to measure the number and area of amyloid plaques. A vehicle (control) group consisted of 13 animals and a compound A treatment group consisted of 16 animals. Nine animals of 8-month old at the initiation of drug administration were used.
2) Results
The quantities of insoluble Aβ40 and 42 proteins in the case that a vehicle or the compound A was administered for six months are shown in
The number and area of amyloid plaques are shown in
According to the present invention, effective agents for treating mild memory impairment can be provided and thereby the progression of mild memory impairment to Alzheimer's disease can be suppressed.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2001-394236 | Dec 2001 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP02/13478 | 12/25/2002 | WO |
