首页> 外国专利> heterocyclic acenapht compound, cyclodextrin inclusion compound of heterocyclic acenapht compound, cyclodextrin complex of heterocyclic acenapht compound, use of heterocyclic acenapht compound, use of cyclodextrin inclusion compound of cyclodextrin and cyclodextrin complex use

heterocyclic acenapht compound, cyclodextrin inclusion compound of heterocyclic acenapht compound, cyclodextrin complex of heterocyclic acenapht compound, use of heterocyclic acenapht compound, use of cyclodextrin inclusion compound of cyclodextrin and cyclodextrin complex use

机译:杂环化合物,杂环化合物的环糊精包合物,杂环化合物的环糊精配合物,杂环化合物的用途,环糊精的环糊精包合物的用途和环糊精的用途

摘要

The present invention relates to acenaphtho heterocyclic compounds, cyclodextrin inclusion compounds and complexes thereof, and their uses in manufacturing the inhibitors of BH3 analogue, Bcl-2 family proteins. The acenaphtho heterocyclic compounds are obtained by introducing oxo-, thio-, carbonyl, ester or acyl in the 3-, 4- and 6-position of 8-oxo-8 H -acenaphtho[1,2-b]pyrrole-9-carbonitrile, or further substituting 9-cyano with carboxyl, ester or amide. The compounds can simulate BH3-only protein, competitively binding and antagonizing Bcl-2, Bcl-X L and Mcl-1 proteins in vitro or intracellularly, to induce cell apoptosis. The cyclodextrin inclusion compounds and complexes can improve the effects. Therefore, they can all be used in the manufacture of anticancer compounds.
机译:本发明涉及杂环化合物,环糊精包合化合物及其配合物,及其在制备BH3类似物Bcl-2家族蛋白抑制剂中的用途。通过在8-氧代-8H-ac [1,2-b]吡咯-9-的3-,4-和6-位引入羰基,硫代,羰基,酯或酰基,获得obtained杂环化合物。腈,或进一步用羧基,酯或酰胺取代9-氰基。这些化合物可以模拟仅BH3蛋白,在体外或细胞内竞争性结合并拮抗Bcl-2,Bcl-XL和Mcl-1蛋白,从而诱导细胞凋亡。环糊精包合物和配合物可以改善效果。因此,它们都可以用于制造抗癌化合物。

著录项

  • 公开/公告号BRPI0921044A2

    专利类型

  • 公开/公告日2019-09-24

    原文格式PDF

  • 申请/专利权人 DALIAN UNIVERSITY OF TECHNOLOGY;

    申请/专利号BR2009PI21044

  • 申请日2009-10-25

  • 分类号C07D209/70;A61K31/403;A61K31/54;A61P43;C07D405/12;C07D409/12;C08B37/16;

  • 国家 BR

  • 入库时间 2022-08-21 12:03:01

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