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Prostacyclin analogs and their use in inhibition of arachidonic acid- induced platelet aggregation and bronchoconstriction

机译:前列环素类似物及其在抑制花生四烯酸诱导的血小板聚集和支气管收缩中的用途

摘要

Prostacyclin analogs are provided having the structure ##STR1## wherein X represents O or OH, R.sub.1 and R.sub.2 are OH or H, provided at least one of R.sub.1 and R.sub.2 is other than hydroxyl, R. sub.3 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## STR1 ##的前列环素类似物,其中X代表O或OH,R 1和R 2是OH或H,条件是R 1和R 2中至少一个。 2不是羟基,R.sub.3是H或1-4个碳的烷基,m是2-5的整数,n是2-10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US4192891A

    专利类型

  • 公开/公告日1980-03-11

    原文格式PDF

  • 申请/专利权人 SQUIBB E R & SONS INC;

    申请/专利号US19790033368

  • 发明设计人 MARTIN F. HASLANGER;

    申请日1979-04-25

  • 分类号C07C177/00;C07C69/38;C07C69/74;

  • 国家 US

  • 入库时间 2022-08-22 17:06:30

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