首页> 外国专利> 2- Or 3-imidazolyl-1-isopropyl-4-methyl cyclohexane derivs. - prepd. by reaction of imidazole with halo- or sulphonyloxy-1-isopropyl-4-methyl-cyclohexane

2- Or 3-imidazolyl-1-isopropyl-4-methyl cyclohexane derivs. - prepd. by reaction of imidazole with halo- or sulphonyloxy-1-isopropyl-4-methyl-cyclohexane

机译:2-或3-咪唑基-1-异丙基-4-甲基环己烷衍生。 -准备咪唑与卤代或磺酰氧基-1-异丙基-4-甲基-环己烷反应

摘要

New imidazole deriv are 2- and 3-(1-imidazolyl) -4- methyl-1-isopropyl-cyclohexane derivs (I), in which the 3 chiral centres have R- or S- configuration, and their racemates, and pharmacologically tolerable salts of these cpds. (I) are inhibitors of thromboxane synthesis, with greater activity than known imidazole derivs. They accordingly modify the thromboxane A2/PGI2 equilibrium in favour of the antiaggregatory, vasodilating PGI2 at the expense of the proaggregatory and vasoconstricting TXA2, and can be used as antithromboembolic agents.
机译:新的咪唑衍生物是2-和3-(1-咪唑基)-4-甲基-1-异丙基-环己烷衍生物(I),其中三个手性中心具有R-或S-构型,以及它们的外消旋体,并且在药理上可耐受这些cpds的盐。 (I)是血栓烷合成的抑制剂,具有比已知的咪唑衍生物更大的活性。他们因此改变了血栓烷A2 / PGI2的平衡,有利于抗凝集,使PGI2血管舒张,而牺牲了凝集和收缩血管的TXA2,并可用作抗血栓栓塞剂。

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