Thiazepinyl hydroxamic acid derivatives as matrix...

C - Chemistry – Metallurgy – 07 – D

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C07D 281/06 (2006.01) A61K 31/55 (2006.01) A61P 29/02 (2006.01) C07D 417/04 (2006.01) C07D 417/06 (2006.01) C07D 417/12 (2006.01) C07D 417/14 (2006.01)

Patent

CA 2400862

A compound of formula (I) in which R1 is halo, lower alkoxy, optionally substituted aryl, optionally substituted aryloxy, optionally substituted heterecyclic group or optionally substituted lower alkynyl, R2 is amidated carboxy, R3 is hydrogen or acyl, Ar is aryl or heterocyclic group, X is thia, sulfinyl or sulfonyl, Y and Z are each lower alkylene, m and n are each an integer of 0 to 2, and a salt thereof, useful as inhibitors of matrix metalloproteinases (MMP) or the production of tumor necrosis factor .alpha. (TNF .alpha.).

L'invention concerne un composé correspondant à la formule (I), ainsi qu'un sel de celui-ci. Dans cette formule R?1¿ représente halo, alcoxy inférieur, aryle éventuellement substitué, aryloxy éventuellement substitué, un groupe hétérocyclique éventuellement substitué ou alcynyle inférieur éventuellement substitué, R?2¿ représente carboxy amidé, R?3¿ représente hydrogène ou acyle, Ar représente aryle ou un groupe hétérocyclique, X représente thia, sulfinyle ou sulfonyle, Y et Z représentent chacun alkylène inférieur, m et n représentent chacun un nombre entier compris entre 0 et 2. Ce composé et son sel sont utiles en tant qu'inhibiteurs des métalloprotéinases matricielles ou dans la production du facteur .alpha. de nécrose tumorale (TNF .alpha.).

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