Prostaglandin F{HD 3{B {331 {0 analogs
    6.
    发明授权
    Prostaglandin F{HD 3{B {331 {0 analogs 失效
    前列腺素F {HD 3 {B {331 {0 analogs

    公开(公告)号:US3879437A

    公开(公告)日:1975-04-22

    申请号:US41295773

    申请日:1973-11-05

    申请人: UPJOHN CO

    发明人: AXEN UDO F

    摘要: This disclosure relates to prostaglandins of the PG3 series including PGE3, PGF3 , PGF3 , and PGB3, to various analogs of those in racemic form, and to novel processes for making those. This disclosure also relates to certain fluorine and alkyl substituted analogs and certain acetylenic analogs of PGE3, PGF3 , PGF3 , PGA3, and PGB3 in both racemic and optically active form, and to processes for making those. These various analogs are useful for the same pharmacological purposes as the known optically active forms of PGE3, PGF3 , PGF3 , and PGB3, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement, fertility control, and wound healing.

    摘要翻译: 本公开涉及包含PGE3,PGF3α,PGF3β和PGB3的PG3系列的前列腺素与外消旋形式的各种类似物,以及制备它们的新方法。 本公开还涉及外消旋和旋光活性形式的某些氟和烷基取代的类似物和PGE3,PGF3α,PGF3β,PGA3和PGB3的某些乙炔类似物,以及制备它们的方法。 这些各种类似物对于与已知的PGE3,PGF3α,PGF3β和PGB3的光学活性形式具有相同的药理学目的是有用的,包括抗溃疡,抑制血小板聚集,增加鼻通气,劳动诱导,生殖调节和 伤口愈合。