首页> 外国专利> ACENAPHTHO HETEROCYCLE COMPOUNDS, CYCLODEXTRIN INCLUSION COMPOUNDS AND COMPLEXES, AND USES IN THE MANUFACTURES OF BH3 PROTEIN ANALOGUE, BCL-2 FAMILY PROTEIN INHIBITORS THEREOF

ACENAPHTHO HETEROCYCLE COMPOUNDS, CYCLODEXTRIN INCLUSION COMPOUNDS AND COMPLEXES, AND USES IN THE MANUFACTURES OF BH3 PROTEIN ANALOGUE, BCL-2 FAMILY PROTEIN INHIBITORS THEREOF

机译:乙炔杂环化合物,环糊精包合物和配合物及其在BH3蛋白类似物,BCL-2家族蛋白抑制剂生产中的用途

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复合物,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。

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