发明名称
摘要 <p>Pyrazolidinedione derivatives of the general formula (I), wherein R1 is hydrogen, optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl or heteroarylalkyl; and R2 is aryl or heteroaryl; tautomers thereof; geometric isomers thereof and tautomers of these geometric isomers, including mixtures of individual compounds of formula (I), or tautomers thereof, and their geometric isomers, or tautomers thereof; pharmaceutically acceptable acid addition salts of compounds which are basic; pharmaceutically acceptable salts of compounds containing acidic groups with bases; pharmaceutically acceptable esters of compounds containing hydroxy or carboxy groups; prodrugs of compounds in which a prodrug forming group is present; as well as hydrates or solvates thereof; are active as platelet adenosine diphosphate receptor antagonists and can be used for the prevention and/or treatment of peripheral vascular, of visceral-, hepaticand renal-vascular, of cardiovascular and of cerebrovascular diseases or conditions associated with platelet aggregation, particularly thrombosis, and, respectively, for the manufacture of corresponding medicaments. Some, albeit not all, of the compounds of the above formula (I) are novel.</p>
申请公布号 JP2007506661(A) 申请公布日期 2007.03.22
申请号 JP20060515947 申请日期 2004.06.16
申请人 发明人
分类号 C07D231/34;A61K31/4152;A61K31/4155;A61K31/4166;A61K31/4178;A61K31/4439;A61K31/454;A61K31/4725;A61K31/5377;A61P7/02;A61P7/04;A61P43/00;C07C45/00;C07C45/62;C07C45/67;C07C45/68;C07C45/71;C07C47/542;C07C47/548;C07C47/565;C07C47/575;C07C309/65;C07D231/32;C07D231/36;C07D401/04;C07D401/06;C07D405/12;C07D409/12 主分类号 C07D231/34
代理机构 代理人
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