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prostacyclin analogues and their use in the inhibition of platelet aggregation induced by arachidonic acid and the broncostenosi

机译:前列环素类似物及其在抑制花生四烯酸和支气管哮喘引起的血小板凝集中的应用

摘要

Prostacyclin analogs are provided having the structure IMAGE wherein X represents =O or OH, R1 and R2 are OH or H, provided at least one of R1 and R2 is other than hydroxyl, R3 is H or alkyl of 1 to 4 carbons, m is an integer of from 2 to 5, and n is an integer of from 2 to 10, or pharmaceutically acceptable salts thereof. These compounds have been found to be potent inhibitors of arachidonic acid-induced platelet aggregation and bronchoconstriction.
机译:提供具有结构的前列环素类似物,其中X表示= O或OH,R 1和R 2为OH或H,条件是R 1和R 2中的至少一个不是羟基,R 3为H或1-4个碳的烷基, m是2至5的整数,或者n是2至10的整数,或其药学上可接受的盐。已经发现这些化合物是花生四烯酸诱导的血小板聚集和支气管收缩的有效抑制剂。

著录项

  • 公开/公告号IT8048486D0

    专利类型

  • 公开/公告日1980-04-22

    原文格式PDF

  • 申请/专利号IT19800048486

  • 发明设计人 MARTIN F.HASLANGER;

    申请日1980-04-22

  • 分类号C07C69/73;A61K31/19;A61K31/215;A61P7/02;A61P11/08;C07C51;C07C59/46;C07C59/90;C07C67;C07C405;C07D309/12;

  • 国家 IT

  • 入库时间 2022-08-22 18:13:41

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