Inhibitors of interleukin-1.beta. converting enzyme

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 487/04 (2006.01) A61K 31/55 (2006.01) A61K 31/675 (2006.01) A61K 38/05 (2006.01) A61K 38/06 (2006.01) C07D 243/10 (2006.01) C07D 243/14 (2006.01) C07D 401/12 (2006.01) C07D 403/12 (2006.01) C07D 405/12 (2006.01) C07D 409/12 (2006.01) C07D 413/12 (2006.01) C07D 417/12 (2006.01) C07D 471/04 (2006.01) C07D 473/00 (2006.01) C07D 491/048 (2006.01) C07D 495/04 (2006.01) C07D 498/04 (2006.01) C07D 513/04 (2006.01) C07D 519/00 (2006.01) C07F 9/645 (2006.01) C07F 9/6561 (2006.01) C07K 5/078 (2006.01) C07K 5/097

Patent

CA 2239904

The present invention relates to novel classes of compounds which are inhibitors of interleukin-1,6 converting enzyme. The ICE inhibitors of this invention are characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting ICE activity and consequently, may be advantageously used as agents against IL-1-, apoptosis-, IGIF-, and IFN-.gamma.- mediated diseases, inflammatory diseases, autoimmune diseases, destructive bone disorders, proliferative disorders, infectious diseases, degenerative diseases, and necrotic diseases. This invention also relates to methods for inhibiting ICE activity, for treating interleukin-1-, apoptosis-, IGIF- and IFN-.gamma.-mediated diseases and decreasing IGIF and IFN-.gamma. production using the compounds and compositions of this invention. This invention also relates to methods for preparing N-acylamino compounds.

L'invention concerne de nouvelles classes de composés qui sont des inhibiteurs de l'enzyme convertissant l'interleukine-1 beta . Ces inhibiteurs ont des caractéristiques structurelles et physicochimiques spécifiques. Cette invention concerne également des compositions pharmaceutiques comprenant ces composés. Les composés et les compositions pharmaceutiques de l'invention conviennent tout particulièrement pour inhiber l'activité de l'enzyme convertissant l'interleukine-1 beta et peuvent donc être utilisés d'une manière avantageuse comme agents contre les maladies provoquées par l'IL-1, l'apoptose, l'IGIF et l'IFNX- gamma , contre les maladies inflammatoires, les maladies auto-immunes, les maladies s'accompagnant d'une destruction du tissu osseux, les maladies s'accompagnant d'une prolifération cellulaire, les maladies infectieuses, les maladies dégénératives et les nécroses. Cette invention concerne également des méthodes pour inhiber l'activité de l'enzyme convertissant l'interleukine-1 beta , pour traiter les maladies provoquées par l'interleukine-1, l'apoptose, l'IGIF et l'IFN- gamma , et pour diminuer la production d'IGIF et d'IFN- gamma en utilisant les composés et les compositions de cette invention. Cette invention concerne également des procédés pour préparer des composés N-acylamino.

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