Novel sulfonyl derivatives

C - Chemistry – Metallurgy – 07 – D

Patent

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C07D 513/04 (2006.01) A61K 31/415 (2006.01) A61K 31/435 (2006.01) A61K 31/44 (2006.01) A61K 31/445 (2006.01) A61K 31/47 (2006.01) A61K 31/495 (2006.01) A61K 31/505 (2006.01) A61K 31/53 (2006.01) A61K 31/535 (2006.01) A61K 31/54 (2006.01) A61K 31/55 (2006.01) C07D 207/04 (2006.01) C07D 207/08 (2006.01) C07D 207/12 (2006.01) C07D 207/22 (2006.01) C07D 209/44 (2006.01) C07D 211/34 (2006.01) C07D 211/70 (2006.01) C07D 213/56 (2006.01) C07D 213/61 (2006.01) C07D 213/73 (2006.01) C07D 213/75 (2006.01) C07D 213/82

Patent

CA 2340100

Sulfonyl derivatives represented by the following general formula (I): Q1-Q2- T1-Q3-SO2-QA and drugs containing the same (wherein Q1 is an optionally substituted, saturated or unsaturated, five- or six-membered cyclic hydrocarbon group, a five- or six-membered heterocyclic group, or the like; Q2 is a single bond, oxygen, sulfur, C1-C6 alkylene or the like; QA is optionally substituted arylalkenyl, heteroarylalkenyl or the like; and T1 is carbonyl or the like). These compounds have potent FXa-inhibitory effects and promptly exert satisfactory and persistent antithrombotic effects through oral administration, thus being useful as anticoagulant agents little accompanied with side effects.

L'invention se rapporte à des dérivés sulfonyle représentés par la formule générale (I) et à des médicaments contenant ces dérivés. Dans la formule (I), Q?1¿-Q?2¿-T?1¿-Q?3¿-SO¿2?-Q?A¿, Q?1¿ est un groupe hydrocarbure cyclique à cinq ou six éléments, saturé ou non saturé et éventuellement substitué, un groupe hétérocyclique à cinq ou six éléments, ou analogue; Q?2¿ est une liaison simple, oxygène, soufre, alkylène C¿1?-C¿6? ou analogue; Q?A¿ est hétéroarylalcényle, arylalcényle éventuellement substitué ou analogue; et T?1¿ est carbonyle ou analogue. Les composés de cette invention sont dotés de puissants pouvoirs inhibiteurs de Fxa et leur administration orale permet d'obtenir des effets antithrombotiques rapides et durables, ce qui les rend utiles en tant qu'agents anticoagulants ne présentant que de faibles effets secondaires.

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