摘要:
The invention relates to specific novel 7-aza-indazoles having formula (I), which modulate the activity of proteins, particularly kinases, compositions containing same and the use thereof as a medicament, in particular as anticancer agents.
摘要:
The invention relates to substituted imidazoles and pyrroles, compositions containing same, the production method thereof and the use of same. More specifically, the invention relates to the preparation of substituted imidazoles and pyrroles, compositions containing same, the preparation method thereof and the use of same as a medicament, particularly as anti-cancer agents.
摘要:
The invention relates to substituted pyrrolo-pyridines, compositions containing them, a method for their production and use thereof. The invention particularly relates to the preparation of pyrrolo-pyridines, compositions containing them, their production method and their use as a medicament, in particular, as anticancer agents. Formula (I).
摘要:
The invention relates to the preparation of substituted indoles, to compositions containing them, to a method for the preparation thereof, and to their use as a medicament, particularly as anticancer agents.
摘要:
The invention relates to substituted imidazoles and pyrroles, compositions containing same, the production method thereof and the use of same. More specifically, the invention relates to the preparation of substituted imidazoles and pyrroles, compositions containing same, the preparation method thereof and the use of same as a medicament, particularly as anti-cancer agents.
摘要:
The invention relates to substituted pyrazolo-pyridines, compositions containing them, a method for the production thereof, and to their use. The invention particularly concerns the preparation of substituted pyrazolo-pyridines, compositions containing them, a method for the preparation thereof, and their use as a medicament, in particular, as anticancer agents.
摘要:
The invention concerns 4-substituted quinoline derivatives active as antimicrobial agents, of general formula (I), wherein: X1, X2, X3, X4 and X5 respectively represent >C-R'1 to >C-R'5, or not more than one represents N; Y represents CHR, CO, CROH, CRNH2, CRF or CF2, R being hydrogen or alkyl; m is 1, 2, or 3 and n is 0, 1 or 2; Z is CH2 or Z represents O, S, SO, SO2 and, in that case, n is equal to 2; R2 represents -CO2R, -CH2CO2R, -CH2-CH2CO2R, -CH2OH or -CH2-CH2OH, R being as defined above; R3 represents phenyl, heteroaryl or alk-R°3, wherein alk is an alkyl and R°3 represents various groups, optionally oxygenated, sulphured or aminated, in their enantiomeric or diastereoisomeric forms or mixtures thereof, and optionally in their syn or anti forms or mixtures thereof, as well as their salts.
摘要:
Quinolyl propyl piperidine deriviatives of general formula (I) wherein R1 is an H or halogen atom or OH, NH2, alkylylamino, dialkylamino, hydroxyamino, alkyloxyamino ou alkylol alkyloxy amino, R2 represents COOH, carboxymethyl or hydroxymethyl, R3 is alkyl (1 - 6 carbon atoms) substituted by phenylthio which can include 1 - 4 substituents [chosen from halogen, OH, alkyl, alkyloxy, trifluoromethyl, trifluoromethoxy, carboxy, alkyloxycarbonyl, cyano or NH2], by a cycloalkylthio radical (3 - 7 membered), or by an aromatic heterocyclylthio radical which is 5 - 6 membered comprising 1 - 4 heteroatoms chosen from nitrogen, oxygen or sulphur and itself optionally substituted [by halogen, OH, alkyl, alkyloxy, trifluoromethyl, trifluoromethoxy, oxo, COOH, alkyloxycarbonyl, cyano or NH2] or R3 is propargyl substituted by phenyl which, itself, can include 1 - 4 substituents [chosen from halogen, OH, alkyl, alkyloxy, trifluoromethyl, trifluoromethoxy, carboxy, alkyloxycarbonyl, CN or NH2], or substituted by cycloalkyl containing 3 -7 members or substituted by aromatic heterocyclyl (5 - 6 members and1 - 4 heteroatoms chosen from nitrogen, oxygen or sulphur) and itself optionally substituted [by halogen, OH, alkyl, alkyloxy, trifluoromethyl, trifluoromethoxy, oxo, COOH, alkyloxycarbonyl, CN or NH2], and R4 is alkyl (1 -6 carbon atoms), alkenyl-CH2- or alkynyl-CH2- (whose alkenyl or alkynyl parts comprise 2 - 6 carbon atoms), cycloalkyl or cycloalkyl alkyl (whose cycloalkyl part comprises 3 -8 carbon atoms) in the diastereoisomer forms thereof or mixtures thereof and/or in the cis or trans forms thereof, in addition to the salts thereof. The novel derivatives are particularly interesting antimicrobial agents.
摘要:
The invention relates to substituted pyrazolo-pyridines, compositions containing them, a method for the production thereof, and to their use. The invention particularly concerns the preparation of substituted pyrazolo-pyridines, compositions containing them, a method for the preparation thereof, and their use as a medicament, in particular, as anticancer agents.