发明名称 Pyridine derivatives
摘要 The pyridine derivatives of the general formula: <IMAGE> I [wherein A represents an alkylene group containing from 1 to 5 carbon atoms unsubstituted or substituted by a hydroxy group, B represents a single bond, or an oxygen or sulphur atom, or an alkylene group containing from 1 to 5 carbon atoms, D represents a single bond, or an alkylene group containing from 1 to 5 carbon atoms, R represents a grouping of the formula: <IMAGE> (in which R6 represents a hydrogen atom, or an alkyl group containing from 1 to 4 carbon atoms), Z represents a single bond, or an ethynylene group, or a grouping of the formula: <IMAGE> in which R2 represents a hydrogen atom, or an alkyl group containing from 1 to 4 carbon atoms, R3 represents a hydrogen, bromine or chlorine atom, or an alkyl group containing from 1 to 4 carbom atoms; the symbol represents a single or double bond, the carbon atom attached to R2 binds to B, and the carbon atom attached to R3 binds to D, R1 represents a hydroxy group, or a grouping of the formula: -COOR4 or -COSR4, in which R4 represents a hydrogen atom, or an alkyl group containing from 1 to 12 carbon atoms, or an aralkyl group containing from 7 to 13 carbon atoms, or a cycloalkyl group containing from 4 to 7 carbon atoms unsubstituted or substituted by at least one alkyl group containing from 1 to 4 carbon atoms, or a phenyl unsubstituted or substituted by at least one halogen atom, trifluoromethyl group, alkyl or alkoxy or alkylthio group containing from 1 to 4 carbon atoms, nitro or phenyl group, R5 represents a hydrogen atom, or an alkyl group containing from 1 to 4 carbon atoms, with the proviso that, when B represents an oxygen or sulphur atom, Z represents a single bond and D represents an alkylene group containing from 1 to 5 carbon atoms], and non-toxic acid addition salts thereof and, when R1 represents a carboxy or thiocarboxy group, non-toxic salts thereof, possess a strong inhibitory activity on thromboxane synthetase from rabbit platelet microsomes, and are useful as therapeutically active agents in the prevention or treatment of inflammation, hypertension, thrombus, cerebral apoplexy, asthma, myocardial infarction, cardiostenosis, cerebral infarction and acute cardiac death.
申请公布号 US4271170(A) 申请公布日期 1981.06.02
申请号 US19790105672 申请日期 1979.12.20
申请人 ONO PHARMACEUTICAL CO., LTD., 发明人 TANOUCHI, TADAO;KAWAMURA, MASANORI;HAYASHI, MASAKI
分类号 C07D213/18;C07D213/30;C07D213/48;C07D213/55;C07D213/57;(IPC1-7):A61K31/44;C07D409/06 主分类号 C07D213/18
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