Patent Application
20150307471
The present invention relates to a compound for use in the treatment of bacterial and mycobacterial infections, such as for example tuberculosis, leprosy and atypical mycobacterial infections.
The present invention also concerns new compounds that can be used as medicament, in particular as medicament in the treatment of bacterial and mycobacterial infections such as, for example, tuberculosis, leprosy and atypical mycobacterial infections.
The present invention also concerns pharmaceutical compositions comprising, as the active ingredient, at least one of the abovementioned compounds and optionally an antibiotic active against bacteria and/or mycobacteria, notably an antibiotic activatable via the EthA pathway, more particularly an antibiotic chosen from the family of thioamides, for example ethionamide or prothionamide.
The present invention also concerns products (kits) containing at least one of the aforementioned compounds and at least one antibiotic active against bacteria and/or mycobacteria, notably an antibiotic activatable via the EthA pathway, more particularly an antibiotic chosen from the family of thioamides, for example ethionamide or prothionamide, as combination products for use simultaneously, separately or spread out in time, in the therapy of tuberculosis, leprosy or general mycobacterial infections
Tuberculosis kills 2 million people every year in the world. The AIDS epidemics and the emergence of strains that are multi-resistant to antibiotics contribute to exacerbating the impact of this illness, considered by the World Health Organization as responsible for an increasingly dangerous worldwide epidemic and as a health emergency on a global scale.
An increasing number of Mycobacterium tuberculosis strains is characterized nowadays by multi-resistance to first-line antibiotics such as isoniazid (INH) and rifampicin (RIF). These antibiotics must then be replaced by second-line antibiotics such as ethionamide (ETH) to which the strains are not resistant but which have the disadvantage of having a low therapeutic index (the therapeutic index of an active ingredient is the ratio of therapeutic dose to toxic dose).
One strategy consisting in increasing the activity of ethionamide (ETH) by associating it to a specific compound has already been considered. In fact, ETH is a prodrug that is transformed in vivo into a therapeutically active form by the EthA enzyme (see the article “Activation of the prodrug ethionamide is regulated in mycobacteria”, A. R. Baulard et al., Journal of Biological Chemistry, 2000, 275, 28326-28331). The observed resistances to ETH arise from the fact that the transcriptional repressor EthR of M. tuberculosis controls the expression of the EthA enzyme and restricts the transformation of ETH into a therapeutically active substance.
One aim of the present invention is to propose new compounds likely to potentiate notably the activity of antibiotics active against tuberculosis, in particular an antibiotic chosen from the thioamide family, such as ethionamide or prothionamide for example.
Another aim of the present invention is to propose compounds such as previously mentioned that, in combination with an antibiotic active against tuberculosis, chosen from the thioamide family, in particular ethionamide and/or prothionamide, and at identical antibiotics dosage, enable a greater efficiency to be achieved or that enable the aforementioned antibiotics dosage to be reduced to achieve a given efficiency.
Another aim of the present invention is to propose compounds such as previously mentioned that are simple and inexpensive to produce.
Another aim of the present invention is to propose compounds such as previously mentioned that are satisfactorily soluble in a biologic fluid.
Another aim of the present invention is to propose compounds such as previously mentioned that are likely to be active in particular orally and/or that cause fewer side effects.
To achieve at least one of the aforementioned aims, the present invention thus proposes compounds of the general formula (I):
in which:
R2 is chosen from the following groups: phenyl, benzyl, phenyl or benzyl groups substituted by at least one linear or branched C1-C4 alkyl chain, phenyl or benzyl groups substituted by at least one linear or branched and substituted C1-C4 alkyl chains, in particular substituted by at least one fluorine atom (F), phenyl groups substituted by at least one group chosen from Cl, F, CF3, OCH3, OCF3, or OH, and the heterocycles having 6 vertices, saturated or unsaturated, comprising one, two or three nitrogen atoms.
Advantageously, m=n=1. Such components in combination with ethionamide prove particularly active on mycobacteria, in particular on M. tuberculosis.
R1 can be chosen from the following groups: —CH2-isopropyl; cyclopropyl, cyclobutyl, cyclopentyl, —CH2-cyclopropyl, —CH2-cyclobutyl, and —CH2-cyclopentyl.
Advantageously, R1 is a —CH2CF3 group. Such components exhibit a good potentiating activity of ethionamide, in particular on M. tuberculosis.
Advantageously, X═CH. Such components have proven more efficient in combination with ethionamide, in particular on the bacterium M. tuberculosis.
According to a first embodiment, R2 is a phenyl group.
According to a second embodiment, R2 is a benzyl group.
According to a third embodiment, R2 is a phenyl group substituted by at least one F atom.
According to a fourth embodiment, R2 is a phenyl group substituted in meta position relative to the bonding to X, by Cl, F, CF3 or CH3.
Advantageously, R2 is a phenyl group substituted in para position relative to its bonding to X by a fluorine atom F.
According to another embodiment. R2 is a group chosen from the following groups:
The inventive compound can be chosen from the following cbmpounds:
The present invention also concerns the aforementioned compound for its use as medicament, in particular for its use in the treatment of bacterial and mycobacterial infections, notably in the treatment of tuberculosis, leprosy or atypical mycobacterial infections.
The present invention also concerns a pharmaceutical composition comprising, as the active ingredient, at least one compound of general formula (I) as previously mentioned and one pharmaceutically acceptable excipient.
Within the pharmaceutical compositions according to the invention, the compound or compounds used as active ingredient(s) can be used in a quantity that enables unit doses comprised between 0.3 mg and 1 g approximately to be administered. Within the pharmaceutical compositions according to the invention, the antibiotic or antibiotics active against mycobacteria are, when present, advantageously used in a quantity enabling the administration of unit doses equal to or lower than the doses usually recommended by the World Health Organization (WHO, Treatment of tuberculosis: Guidelines for National Programs. 2003; WHO/CDS/TB2003.313.), national or non-governmental health organizations or the competent pharmaceutical laboratories.
The one skilled in the art is able to choose one or several pharmaceutically acceptable excipients depending on the route of administration of the pharmaceutical composition. The one skilled in the art will of course ensure in doing so that the excipient or excipients used are compatible with the intrinsic properties attached to the composition according to the present invention. Furthermore, the form of the medicament or pharmaceutical composition (for example a solution, a suspension, an emulsion, tablets, capsules, suppositories etc.) will depend on the chosen administration route.
Thus, in the sense of the present invention, the medicament or pharmaceutical composition can be administered by any appropriate route, for example oral, anal, local (topical for example), systemic, intravenous, intramuscular or mucosal route, or else by using a patch, or else in encapsulated form in or immobilized on liposomes, microparticles, microcapsules, associated to nanoparticles and similar. By way of non-limiting examples of excipients suitable for administration by the oral route, one can notably cite talcum, lactose, starch and its derivatives, cellulose and its derivatives, polyethylene glycols, acrylic acid polymers, gelatin, magnesium stearate, animal, vegetal or synthetic fats, paraffin derivatives, glycols, stabilizers, preservatives, anti-oxidants, wetting agents, anti-caking agents, dispersants, emulsifiers, taste modifying agents, penetrating agents, solubilizing agents etc. The formulation and administration techniques for the medicaments and pharmaceutical compositions are well known in the art here under consideration, the one skilled in the art can notably refer to the work Remington's Pharmaceutical Sciences, latest edition.
The present invention also has the aim of using at least one compound according to the invention for the manufacture of a medicament intended for the prevention and/or treatment of bacterial infections, preferably mycobacterial infections, and more particularly of tuberculosis, leprosy or atypical mycobacterial infections.
Advantageously, the pharmaceutical composition further comprises, as active ingredient, at least one antibiotic active against bacteria and/or mycobacteria, in particular an antibiotic activatable via the EthA pathway, more particularly an antibiotic chosen notably from the thioamide family, in particular from ethionamide and prothionamide.
However, the invention is not limited to these antibiotics.
The inventive compounds prove to be compounds potentiating antibiotics activatable via the EthA pathway; however, the inventive compounds can also be used as potentiating agents of the antibiotic activity of antibiotics that can be bio-activated via another bio-activation pathway or pathways than the aforementioned one.
The present invention also concerns a kit or product containing at least one compound of formula (I) and at least one antibiotic active against bacteria and/or mycobacteria in particular, in particular an antibiotic activatable via the enzymatic EthA pathway, more particularly an antibiotic chosen from the thioamide family, in particular chosen from ethionamide and prothionamide as combination products for use, simultaneously, separately or spread out in time, in the therapy of tuberculosis, leprosy or general mycobacterial infections.
Within the whole of the present application, when it is not indicated that a group, whatever it is, is substituted, the latter is not substituted.
Within the meaning of the present invention, a substituted phenyl group is defined as a mono-, di- or tri-substituted phenyl group. The position of the substituent or substituents, when it is not indicated, is not limited according to the invention. When the substituent or substituents are indicated, the phenyl group can also comprise one or several other substituents different from those mentioned.
Preferably, the phenyl groups substituted by Cl, CF3, and CH3 are mono-substituted and the substituent (Cl, CF3 or CH3) is preferably in meta position relative to the carbon of the benzene cycle bound to X. Preferably, X is CH.
In the case of a phenyl group substituted by a fluorine atom, all the groups mono-, di- or tri-substituted by fluorine atoms are included in the present invention. Advantageously, the phenyl groups substituted by one or several fluorine atoms are not substituted by another group or by another atom other than F. Thus, phenyl groups substituted by at least one fluorine atom include, within the meaning of the present invention, phenyl groups mono-substituted by a fluorine atom, situated in ortho, meta or para position of the carbon of the benzene cycle bound to X, phenyl groups substituted by two fluorine atoms, in particular phenyl groups substituted by two fluorine atoms placed in ortho and para position of the bond of the benzene cycle with X, phenyl groups having three carbon atoms substituted each by a fluorine atom, in particular a phenyl group tri-substituted by three fluorine atoms of which two fluorine atoms are in ortho position of the bond of the benzene cycle with X and one fluorine atom is in para position relative to this bond.
Atypical mycobacterial infections are defined here as mycobacterial infections caused by at least one mycobacterium other than M. Tuberculinum and in particular mycobacterial infections involving M. Kansasii.
According to the present invention, the term “treatment” designates the curative treatment and/or prophylactic treatment of the aforementioned infections. The term “treatment” includes all improvement of the patient's state, in particular any diminution of the number of bacteria present in at least one infection site of the patient.
Within the meaning of the present invention, an antibiotic active against bacteria and/or mycobacteria is defined as any agent capable of limiting or reducing at least in vitro the proliferation of a bacterium and/or of a mycobacterium, in particular M. tuberculosis. An agent capable of destroying, at least in vitro, a mycobacterium, notably M. tuberculosis, is also an antibiotic active against mycobacteria within the meaning of the present invention. Among the antibiotics active against mycobacteria and activatable via the enzymatic EthA pathway, ethionamide, prothionamide, isoxyl, thiacetazone and the mixtures of at least two of these antibiotics can be mentioned.
In the present invention, an antibiotic activatable via the EthA pathway is defined as any substance that at least in vitro reacts with the EthA enzyme to produce a substance having antibiotic properties. The one skilled in the art is able to determine if an antibiotic is activatable by the EthA pathway for example by applying the method described in the following publication: “Activation of the prodrug ethionamide is regulated in mycobacteria” A. R. Baulard et al., Journal of Biological Chemistry, 2000, 275, 28326-28331.
The antibiotic within the meaning of the present invention can also be an antibiotic activatable via another bio-activation pathway than the aforementioned one.
Nuclear magnetic resonance spectra (NMR) 1H and 13C were performed at ambient temperature on a Bruker™ DPX 300 spectrometer at 300 MHz. The chemical shifts are expressed in parts per million (ppm). The assignments have been performed using 1H and 13C one-dimensional (1D) or two-dimensional (2D) HSQC-COSY experiments. Mass spectra were performed on an LCMS Waters Alliance Micromass ZQ 2000 system. The commercial reagents and solvents were used without ulterior purification.
The LDA (solution at 2M in THF/heptane/ethyl benzene, 3.3 mmole 1.1 eq) is added with 5 mL anhydrous THF in a flask previously oven-dried and put under argon. The solution is cooled to −78° C. The N-Boc-4-piperidone (or N-Boc-3-pyrrolidinone) (3 mmol, 1 eq) dissolved in 5 mL THF is added drop-wise, then the reaction medium is agitated for 20 minutes at −78° C. The N-phenyl-trifluoromethane-sulphonimide (3.3 mmol, 1.1 eq) dissolved in 5 mL THF is added. The solution is agitated 2 h at 0° C. and then evaporated. The residue is dissolved in a mixture of cyclohexane/AcOEt 9:1 and then filtrated on alumina. The product (triflate) is used in the next step without purification.
In a flask containing the triflate (1 eq) and put under argon, one adds the boronic acid (1.1 eq), LiCl (3 eq), the 2N solution of Na2CO3 (1.4 eq), the DME (0.34 M) and the tetrakis(triphenylphosphine)palladium (0.05 eq). The solution is heated between 1 h and 16 h under reflux and then evaporated. The residue is taken up in AcOEt and then washed once using water and once using a solution saturated with NaCl. The organic phase is dried and then evaporated. The residue is taken up in AcOEt and then filtrated on sintered glass. The solvent is evaporated, then the product is purified using chromatography on silica gel (cyclohexane/AcOEt).
The unsaturated derivative (1 eq) is dissolved in ethanol (0.1M) with PtO2 (0.1 eq) or Pd/C (0.1 eq). The reaction mixture is put under hydrogen and agitated at ambient temperature until the input product has disappeared. The solution is filtrated on celite, then evaporated.
Or: the unsaturated derivative (1 eq) is dissolved in methanol (0.1M) with ammonium formate (5 eq) and Pd/C (10% by mass). The reaction mixture is heated under reflux until the input product has disappeared. The solution is filtrated on celite and then evaporated. The protected amine (1 eq.) is added in a flask with dioxane (1 M), then a solution of HCl 4N in dioxane (5 eq) is added. The solution is agitated 1 h at ambient temperature, then evaporated. The residue is taken over in light petroleum and then filtrated on sintered glass.
The acid (1.3 eq) is activated using EDCl (1.3 eq) and HOBt (0.4 eq) in DMF (0.25 M) in the presence of DEIA (4 eq) and then the amine (1 eq) is added. The solution is agitated 3 h at ambient temperature and then evaporated. The residue is dissolved in AcOEt and then washed twice using saturated NaHCO3, twice using HCl 1N and once using saturated NaCl. The organic phase is dried on MgSO4 and then evaporated. The residue is purified using preparative HPLC.
The acid (1.3 eq) is activated using EDCl (1.3 eq) and HOBt (0.4 eq) in DMF (0.25 M) in the presence of DIEA (4 eq), then the commercially available piperazine (1 eq) is added. The solution is agitated 3 h at ambient temperature, then evaporated. The residue is dissolved in AcOEt, then washed twice using saturated NaHCO3, twice using HCl 1N and once using saturated NaCl. The organic phase is dried on MgSO4 then evaporated. The residue is purified using preparative HPLC.
4-phenylpiperidine is commercially available. Only the coupling has been performed.
1H NMR (CD2Cl2) δ 7.36-7.31 (m, 2H), 7.25-7.21 (m, 3H), 4.78-4.71 (m, 1H), 3.99-3.93 (m, 1H), 3.22-3.12 (m, 1H), 2.84-2.48 (m, 6H), 1.96-1.86 (m, 2H), 1.72-1.56 (m, 2H). MS [M+H]+ m/z 286.
4-phenylpiperidine is commercially available. Only the coupling has been performed.
1H NMR (CD2Cl2) δ 7.36-7.31 (m, 2H), 7.25-7.20 (m, 3H), 4.78-4.72 (m, 1H). 3.99-3.92 (m, 1H), 3.19-3.09 (m, 1H), 2.81-2.60 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 2.29-2.16 (m, 2H), 1.97-1.87 (m, 4H), 1.70-1.54 (m, 2H). MS [M+H]+ m/z 300.
1H NMR (CDCl3) δ 7.34-7.28 (m, 2H), 6.97-6.94 (m, 3H), 3.83-3.80 (m, 2H), 3.67-3.64 (m, 2H), 3.24-3.17 (m, 4H), 2.68-2.49 (m. 4H). MS [M+H]+ m/z 287.
1H NMR (CDCl3) δ 7.34-7.28 (m, 2H), 6.97-6.94 (m, 3H), 3.82-3.79 (m, 2H), 3.65-3.62 (m, 2H), 3.22-3.16 (m, 4H), 2.48 (t, J=7.2 Hz, 2H), 2.31-2.15 (m, 2H), 2.03-1.92 (m, 2H).
MS [M+H]+ m/z 301.
1H NMR (CD2Cl2) δ 7.27-7.20 (m, 2H), 7.16-7.03 (m, 2H), 4.79-4.73 (m, 1H). 3.98-3.93 (m, 1H), 3.24-3.08 (m, 2H), 2.74-2.48 (m, 5H), 1.95-1.86 (m, 2H), 1.74-1.63 (m, 2H).
MS [M+H]+ m/z 304.
1H NMR (CD2Cl2) δ 7.27-7.20 (m, 2H), 7.16-7.02 (m, 2H), 4.79-4.74 (m, 1H), 3.99-3.94 (m, 1H), 3.24-3.09 (m, 2H), 2.75-2.49 (m. 5H), 1.95-1.86 (m, 2H). 1.75-1.59 (m, 2H).
MS [M+H]+ m/z 304.
1H NMR (CD2Cl2) δ 7.33-7.19 (m, 2H), 7.06-7.00 (m, 2H), 4.77-4.72 (m, 1H), 3.98-3.92 (m, 1H), 3.21-3.11 (m, 1H), 2.83-2.49 (m. 6H), 1.94-1.86 (m, 2H). 1.68-1.46 (m, 2H).
13C NMR (CD2Cl2) δ 167.64, 161.45 (d, J=244 Hz), 141.20, 127.42 (q, J=274 Hz), 128.16 (d, J=8 Hz), 115.11 (d, J=21 Hz), 45.83, 42.40, 41.91, 33.81, 32.96, 29.53 (q, J=29 Hz), 25.79. MS [M+H]+m/z 304.
1H NMR (CD2Cl2) δ 6.69 (t, J=8.7 Hz, 2H), 4.78-4.72 (m, 1H), 3.98-3.92 (m, 1H), 3.27-3.10 (m, 2H). 2.68-2.48 (m, 5H), 2.07-1.90 (m, 2H), 1.82-1.74 (m. 2H). MS [M+H]+ m/z 340.
1H NMR (CD2Cl2) δ 7.04-6.98 (m, 2H), 6.95-6.90 (m, 2H), 3.79-3.75 (m, 2H), 3.64-3.61 (m, 2H), 3.14-3.07 (m, 4H), 2.61-2.46 (m, 4H). MS [M+H]+ m/z 305.
1H NMR (CD2Cl2) δ 7.04-6.98 (m, 2H), 6.94-6.89 (m, 2H), 3.77-3.74 (m, 2H), 3.62-3.59 (m, 2H), 3.12-3.06 (m, 4H), 2.45 (t, J=7.2 Hz, 2H), 2.25-2.15 (m, 2H), 1.97-1.87 (m, 2H).
MS [M+H]+ m/z 319.
1H NMR (CD2Cl2) δ 6.99-6.82 (m, 3H), 3.79-3.76 (m, 2H), 3.64-3.61 (m, 2H), 3.05-2.99 (m, 4H), 2.67-2.48 (m, 4H). MS [M+H]+ m/z 323.
1H NMR (CD2Cl2) δ 7.41-7.39 (m, 1H), 7.32-7.17 (m, 3H), 4.80-4.75 (m, 1H), 3.99-3.94 (m, 1H), 3.35-3.17 (m, 2H), 2.76-2.49 (m, 5H), 1.99-1.89 (m, 2H), 1.66-1.53 (m, 2H).
MS [M+H]+ m/z 320.
1H NMR (CD2Cl2) δ 7.32-7.21 (m, 3H), 7.15-7.13 (m, 1H), 4.78-4.72 (m, 1H), 3.98-3.93 (m, 1H), 3.21-3.11 (m, 1H), 2.83-2.48 (m, 6H), 1.95-1.87 (m, 2H), 1.69-1.52 (m, 2H).
MS [M+H]+ m/z 320.
1H NMR (CD2Cl2) δ 7.33-7.30 (m, 2H), 7.20-7.17 (m, 2H), 4.78-4.71 (m, 1H), 3.99-3.92 (m, 1H), 3.21-3.11 (m, 1H), 2.82-2.48 (m, 6H), 1.94-1.86 (m, 2H), 1.67-1.51 (m, 2H).
MS [M+H]+ m/z 320.
1H NMR (CD2Cl2) δ 7.28-7.23 (m, 2H), 6.91-6.86 (m, 2H), 3.78-3.75 (m, 2H), 3.64-3.61 (m, 2H), 3.20-3.13 (m, 4H), 2.67-2.46 (m, 4H). MS [M+H]+ m/z 321.
1H NMR (CD2Cl2) δ 7.27-7.22 (m, 2H), 6.91-6.86 (m, 2H), 3.77-3.74 (m, 2H), 3.62-3.59 (m, 2H), 3.18-3.12 (m, 4H), 2.45 (t, J=7.2 Hz, 2H), 2.31-2.15 (m, 2H), 1.97-1.87 (m, 2H).
MS [M+H]+ m/z 335.
1H NMR (CDCl3) δ 7.39 (d, J=8.3 Hz, 1H), 7.29 (d, J=2.0 Hz, 1H), 7.04 (dd, J=8.3 Hz, J=2.0 Hz, 1H), 4.82-4.77 (m, 1H), 4.00-3.94 (m, 1H), 3.21-3.12 (m, 1H), 2.79-2.48 (m, 6H), 1.96-1.88 (m, 2H), 1.67-1.51 (m, 2H).
13C NMR (CDCl3) δ 167.99, 145.10, 132.60, 130.58, 128.84, 127.11 (q, J=275 Hz), 126.11, 45.74, 42.40, 41.90, 33.48, 32.53, 29.69 (q, J=29 Hz), 25.95. MS [M+H]+ m/z 354.
1H NMR (CD2Cl2) δ 7.68 (d, J=4.5 Hz, 1H), 7.58 (t, J=4.5 Hz, 1H), 7.46 (d, J=4.5 Hz, 1H), 7.37 (t. J=4.5 Hz, 1H), 4.81-4.77 (m, 1H), 4.00-3.97 (m, 1H), 3.23-3.17 (m, 2H), 2.73-2.52 (m, 5H), 1.92-1.85 (m, 2H), 1.75-1.68 (m, 2H). MS [M+H]+ m/z 354.
1H NMR (CD2Cl2) δ 7.51-7.46 (m, 4H), 4.80-4.75 (m, 1H), 4.01-3.95 (m, 1H). 3.23-3.14 (m, 1H), 2.93-2.82 (m, 1H), 2.74-2.50 (m, 5H), 1.99-1.90 (m, 2H), 1.74-1.57 (m, 2H).
13C NMR (CD2Cl2) δ 167.72, 146.30, 130.56 (q, J=32 Hz), 130.37, 129.09, 127.44 (q, J=275 Hz), 124.35 (q, J=275 Hz), 123.51 (q, J=4 Hz), 123.25 (q, J=4 Hz), 45.73, 42.48, 42.29, 33.46, 32.63, 29.52 (q, J=28 Hz), 25.83. MS [M+H]+ m/z 354.
1H NMR (CD2Cl2) δ 7.61 (d, J=8.4 Hz, 2H), 7.37 (d, J=8.4 Hz, 2H), 4.80-4.74 (m, 1H), 4.01-3.95 (m, 1H), 3.23-3.13 (m, 1H), 2.92-2.82 (m, 1H), 2.73-2.48 (m, 5H), 1.98-1.89 (m, 2H), 1.73-1.61 (m, 2H). MS [M+H]+ m/z 354.
1H NMR (CD2Cl2) δ 7.19-7.09 (m, 4H), 4.80-4.74 (m, 1H), 4.00-3.94 (m, 1H), 3.23-3.14 (m, 1H), 3.06-2.95 (m, 1H), 2.74-2.47 (m, 5H), 2.38 (s, 3H), 1.88-1.80 (m, 2H), 1.71-1.54 (m, 2H). MS [M+H]+ m/z 300.
1H NMR (CD2Cl2) δ 7.23-7.20 (m, 1H), 7.06-7.01 (m, 3H), 4.77-4.71 (m, 1H), 3.98-3.92 (m, 1H), 3.20-3.11 (m, 1H), 2.79-2.46 (m, 6H), 2.33 (s, 3H), 1.94-1.85 (m, 2H), 1.71-1.53 (m, 2H). MS [M+H]+ m/z 300.
1H NMR (CD2Cl2) δ 7.16-7.10 (m, 4H), 4.77-4.70 (m, 1H), 3.97-3.91 (m, 1H). 3.20-3.10 (m, 1H), 3.06-2.95 (m, 1H), 2.77-2.47 (m, 5H), 2.33 (s, 3H), 1.93-1.85 (m, 2H), 1.69-1.51 (m, 2H). MS [M+H]+ m/z 300.
1H NMR (CD2Cl2) δ 7.25-7.15 (m, 2H), 6.98-6.91 (m, 2H), 4.78-4.72 (m, 1H), 3.97-3.92 (m, 1H), 3.86 (s, 3H), 3.28-3.14 (m, 2H), 2.75-2.47 (m, 5H), 1.94-1.84 (m, 2H), 1.69-1.54 (m, 2H).
13C NMR (CD2Cl2) δ 167.59, 156.89, 133.37, 127.49 (q, J=275 Hz), 127.18, 126.35, 120.56, 110.44, 55.23, 46.16, 42.73, 35.54, 32.31, 31.48, 29.59 (q, J=29 Hz), 25.81.
MS [M+H]+ m/z 316.
1H NMR (CD2Cl2) δ 7.27-7.22 (m, 1H), 6.83-6.76 (m, 3H), 4.78-4.71 (m, 1H), 3.99-3.92 (m, 1H), 3.80 (s, 3H), 3.20-3.11 (m, 1H), 2.81-2.47 (m, 6H), 1.95-1.87 (m, 2H). 1.71-1.54 (m, 2H). MS [M+H]+ m/z 316
1H NMR (CD2Cl2) δ 7.17-7.14 (m, 2H), 6.89-6.86 (m, 2H), 4.76-4.71 (m, 1H). 3.97-3.92 (m, 1H), 3.79 (s, 3H), 3.20-3.11 (m, 1H), 2.74-2.50 (m, 6H), 1.93-1.86 (m, 2H), 1.63-1.55 (m, 2H).
13C NMR (CD2Cl2) δ 168.38, 158.58, 138.06, 127.49 (q, J=275 Hz), 127.56, 113.81, 55.16, 45.97, 42.53, 41.76, 34.06, 33.12, 29.56 (q, J=29 Hz), 25.80. MS [M+H]+ m/z 316.
1H NMR (MeOD) δ 7.08 (dd, J=7.6 Hz, J=1.5 Hz, 1H), 7.00 (td, J=7.6 Hz, J=1.7 Hz, 1H), 6.80-6.74 (m, 2H), 4.71-4.64 (m, 1H), 4.09-4.02 (m, 1H), 3.27-3.15 (m, 2H), 2.80-2.70 (m, 3H), 2.58-2.47 (m, 2H), 1.96-1.83 (m, 2H), 1.74-1.53 (m, 2H). MS [M+H]+ m/z 302.
1H NMR (MeOD) δ 7.04 (d, J=8.7 Hz, 2H), 6.72 (d, J=8.7 Hz, 2H), 4.67-4.61 (m, 1H), 4.04-3.98 (m, 1H), 3.21-3.12 (m, 1H), 2.75-2.66 (m, 4H), 2.58-2.46 (m, 2H). 1.89-1.79 (m, 2H), 1.67-1.44 (m, 2H). MS [M+H]+ m/z 302.
1H NMR (CD2Cl2) δ 8.52 (d, J=6.1 Hz. 2H), 7.16 (d, J=6.1 Hz, 2H), 4.80-4.73 (m, 1H), 4.01-3.93 (m, 1H), 3.22-3.13 (m, 1H), 2.84-2.48 (m, 6H), 1.98-1.89 (m, 2H), 1.71-1.54 (m, 2H). MS [M+H]+ m/z 287.
4-benzoylpiperidine is commercially available. Only the coupling has been performed.
1H NMR (CD2Cl2) δ 7.33-7.28 (m, 2H), 7.24-7.16 (m, 3H), 4.59-4.51 (m, 1H), 3.82-3.77 (m, 1H), 3.02-2.92 (m, 1H), 2.59-2.47 (m, 7H), 1.85-1.67 (m, 3H), 1.24-1.07 (m, 2H).
MS [M+H]+ m/z 300.
1H NMR (CD2Cl2) δ 7.35-7.26 (m, 5H), 3.61 (t, J=5.1 Hz, 2H), 3.54 (s, 2H), 3.45 (t, J=5.1 Hz, 2H), 2.61-2.41 (m, 8H). MS [M+H]+ m/z 301.
1H NMR (CDCl3) δ 7.24-7.18 (m, 2H), 7.07-7.00 (m, 2H), 4-09-3.99 (m, 0.5H), 3.91-3.81 (m, 1H), 3.72-3.64 (m, 0.5H), 3.60-3.31 (m, 3H), 2.61-2.50 (m. 4H), 2.46-2.27 (m, 1H), 2.16-1.95 (m, 1H). MS [M+H]+ m/z 290.
1H NMR (CDCl3) δ 7.34-7.28 (m, 2H), 6.97-6.90 (m, 3H), 3.80 (t, J=5.1 Hz, 2H), 3.66 (t, J=5.1 Hz, 2H), 3.22-3.15 (m, 4H), 2.42-2.37 (m, 2H), 1.70-1.53 (m, 3H), 0.95 (d, J=6.3 Hz, 6H). MS [M+H]+ m/z 261.
1H NMR (CDCl3) δ 7.26-7.22 (m, 2H), 6.91-6.86 (m, 2H), 3.74 (t, J=5.1 Hz, 2H), 3.63 (t, J=5.1 Hz, 2H), 3.18-3.11 (m, 4H), 2.39-2.34 (m, 2H), 1.67-1.49 (m, 3H), 0.95 (d, J=6.3 Hz, 6H). MS [M+H]+ m/z 295.
1H NMR (CDCl3) δ 7.04-6.98 (m, 2H), 6.94-6.90 (m, 2H), 3.74 (t, J=5.1 Hz, 2H), 3.63 (t, J=5.1 Hz, 2H), 3.12-3.05 (m, 4H), 2.39-2.34 (m, 2H), 1.64-1.49 (m, 3H), 0.95 (d, J=6.6 Hz, 6H). MS [M+H]+ m/z 279.
4-phenylpiperidine is commercially available. Only the coupling has been performed.
1H NMR (CD2Cl2) δ 7.36-7.31 (m, 2H), 7.25-7.20 (m, 3H), 4.77-4.73 (m, 1H), 4.02-3.98 (m, 1H), 3.18-3.09 (m, 1H), 2.81-2.71 (m, 1H), 2.66-2.57 (m, 1H), 2.39-2.34 (m, 2H), 1.94-1.85 (m, 2H), 1.69-1.51 (m, 5H), 0.95 (d, J=6.4 Hz, 6H). MS [M+H]+ m/z 260.
The test used makes it possible to ascertain that these compounds are capable of potentiating the bactericide activity of ethionamide on M. tuberculosis alone. This test is a “High Content Screening” (HCS) or dense content screening test. HCS tests are performed on cell cultures that enable certain phenotypic features of a microorganism (e.g. a bacterium) in a given environment to be studied. The phenotypic changes observed can range from the increase (or decrease) of the production of certain marked proteins to the modification of the morphology of the microorganism under consideration. The method is described in the following publication: “Ethionamide Boosters: Synthesis, Biological Activity, and Structure—Activity Relationships of a Series of 1,2,4-Oxadiazole EthR Inhibitors”, M. Flipo et al., Journal of Medicinal Chemistry, 2011, 54(8), 2994-3010.
This test aims to determine the ligand concentration necessary to potentiate ten times the activity of ethionamide (ETH).
To measure the ligand concentration necessary for potentiating ten times the activity of ETH, a constant concentration of ethionamide (0.1 μg/mL corresponding to 1/10th of its CMI99) is chosen. By varying the ligand concentration, the concentration necessary to inhibit 50% of the bacterial growth. i.e. the concentration necessary to potentiate ten times the activity of ethionamide, can be determined. This concentration will be denoted EC50.
40 μL of a solution at 10 mM in DMSO of the sample are added to 1.96 mL MeOH or PBS at pH 7.4. The samples are then agitated during 24 h at RT, centrifuged during 5 min and then filtrated on filters of 0.45 μm size. 20 μL of each solution are then added to 180 μL MeOH and then analyzed by LC-MS. The solubility is determined as ratio of the surfaces of the mass signals PBS/MeOH.
The tables I to III hereafter summarize the formulas of the inventive compounds tested as well as the values of the EC50 experimentally measured according to the aforementioned protocol.
With reference to the results of Table I, one observes that a CH2CF3 group affords a greater potentiating activity of ethionamide without negatively affecting the compound's solubility.
The results show that for a same radical R1 and a same radical R2, the potentiating activity of the inventive compounds is improved when n=1.
Table III hereafter summarizes the activities expressed in EC50 for all the inventive compounds tested.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12/03548 | Dec 2012 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/077732 | 12/20/2013 | WO | 00 |
