Abstract:
Compounds of formula (I): in which: > R1, R2 and R3, as described in the description, form a ring of formula (II) where R6 is a hydrogen or halogen atom, or an alkyl, alkoxy, amino, alkylamino or dialkylamino group, and X is a hydrogen atom or an N-OR7 group, > R4 and R5 are a hydrogen or halogen atom, or an alkyl, alkoxy, alkylamino or dialkylamino group, > A is as defined in the description, > B is an alkyl or alkenyl group substituted with a [-CHR8R9 group.
Abstract:
Compounds of formula (I): in which: R1 is an alkyl, alkenyl, haloalkyl, polyhaloalkyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heteroaryl or heteroarylalkyl, and R2 and R3 are a hydrogen atom or an alkyl group. Medicaments.
Abstract:
Compounds of formula (I): in which: R1 is alkyl, alkenyl, haloalkyl, polyhaloalkyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heteroaryl or heteroarylalkyl, and R2 is a fluorine atom or an alkyl group substituted with one or more fluorine atoms. Medicaments.
Abstract:
The invention concerns compounds of formula (I), wherein: R 1 , R 2 , R 3 , R 4 and X are such as defined in the description; A represents an alkylene chain such as defined in the description; B represents an alkyl or alkenyl group substituted by a group (II) or R 7 , or B represents a group (III) or R 7 . The invention is applicable to preparation of medicines.
Abstract:
Compounds of formula (I), where: R1, R2, R3, R4 are as defined in the description, the enantiomers, diastereomers, tautomers and addition salts thereof with a pharmaceutically-acceptable acid or base. Said compounds have kinase modulating properties and are useful in the treatment of cancer, diabetes, obesity etc.
Abstract:
La présente invention concerne les composés de formule (I) : (voir formule I) dans laquelle : ~ R Cy représente un groupement cycloalkyle ou un groupement cycloalkylalkyle non-substitué ou substitué, ~ R1, R2, R3 et R4, identiques ou différents, représentent chacun un atome d'hydrogène ou d'halogène ou un groupement nitro ; cyano ; hydroxy ; alkoxy ; alkyle ; amino non-substitué ou substitué ; carboxy ; alkoxycarbonyle ; aryloxycarbonyle ; aminocarbonyle non-substitué ou substitué. La présente invention concerne également leurs procédés de préparation, les compositions pharmaceutiques qui les contiennent ainsi que leur utilisation en tant que modulateurs allostériques positifs des récepteurs AMPA.
Abstract:
Phenyl-carbamic acid piperidin-3-yl ester compounds (I) and their enantiomers, and addition salts with an acid or a base are new. Phenyl-carbamic acid piperidin-3-yl ester compounds of formula (I) and their enantiomers, and addition salts with an acid or a base are new. R 1> : H or methyl group; and R 2> : Br, F or CF 3. An independent claim is included for the preparation of (I). [Image] ACTIVITY : Nootropic. MECHANISM OF ACTION : None given.
Abstract:
Compuesto de fórmula (I): (Ver fórmula I) en la que: R1 representa un átomo de hidrógeno o un grupo metilo, R2 representa un átomo de bromo, un átomo de flúor o un grupo trifluorometilo.