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New derivatives 0 - 1 and s - glycosides novel bicyclic lactol, for their preparation and pharmaceutical compositions containing them,

机译:新的衍生物0-1和s-糖苷新型双环丙二醇及其制备方法和包含它们的药物组合物,

摘要

Racemic or optically active compounds with antitumor activity of the formula: IMAGE wherein X is oxygen or sulfur; R1 is hydrogen, C1 to C4 alkanoyl, benzoyl or phenyl-substituted benzoyl; R2 is hydrogen or C1 to C4 alkanoyl; R3 is C2 to C40 straight or branched chain alkyl substituted by hydroxy, epoxy, amino, C1 to C6 alkylamino, C1 to C6 dialkylamino, C1 to C6 alkanoyloxy or, C1 to C4 alkoxycarbonyl; cyclohexyl, phenyl unsubstituted or substituted by halogen, amino, C1 to C4 alkyl-substituted amino, C1 to C4 alkoxy, nitro, or hydroxy; C1 to C6 alkanoyl; allyl or phenyl-C1 to C4 alkyl unsubstituted or substituted by a C2 to C6 alkene group; or where X is sulfur R3 is as defined above or is C1 to C40 straight or branched chain alkyl; and DIFFERENCE represents the exo- or endo-steric position in the ring and indicates an alpha - or beta -steric position in the side chain are disclosed.
机译:具有下式的抗肿瘤活性的外消旋或旋光活性化合物:式中,X为氧或硫; R1是氢,C1至C4的烷酰基,苯甲酰基或苯基取代的苯甲酰基; R2是氢或C1-C4烷酰基; R3是被羟基,环氧基,氨基,C1-C6烷基氨基,C1-C6二烷基氨基,C1-C6链烷酰氧基或C1-C4烷氧基羰基取代的C2-C40直链或支链烷基;环己基,未被取代或被卤素,氨基,C1至C4烷基取代的氨基,C1至C4烷氧基,硝基或羟基取代的苯基; C1至C6烷酰基;未取代或被C 2至C 6烯基取代的烯丙基或苯基-C 1至C 4烷基;或其中X是硫,R 3如上定义或为C 1至C 40直链或支链烷基;或以及“差异”表示环中的外或内空间位置,并表示公开了侧链中的α-或β-空间位置。

著录项

  • 公开/公告号FR2404004B1

    专利类型

  • 公开/公告日1982-12-17

    原文格式PDF

  • 申请/专利权人 CHINOIN GYOGYSZER ES VEGYESZETI;

    申请/专利号FR19780027399

  • 发明设计人

    申请日1978-09-25

  • 分类号C07D307/77;A61K31/34;C07C177/00;

  • 国家 FR

  • 入库时间 2022-08-22 10:02:12

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