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二苯硫醚和二苯硒醚的生物活性及分子模拟

Bioactivity and molecular modelling of diphenylsulfides and diphenylselenides.

作者信息

Woods J A, Hadfield J A, McGown A T, Fox B W

机构信息

CRC Department of Experimental Chemotherapy, Pateson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.

出版信息

Bioorg Med Chem. 1993 Nov;1(5):333-40. doi: 10.1016/s0968-0896(00)82139-2.

Abstract

Bis(2-bromo-4,5-dimethoxyphenyl)sulfide (5) and bis(2-bromo-4,5-dimethoxyphenyl) selenide (7) have been shown to block cells in the G2/M phase of the cell cycle, whereas the debromo (4,6) equivalents do not. The biobromoselenide (7) is cytotoxic to tumour cells in vitro and has been shown to increase the mitotic index of treated cells. These biological effects are consistent with disruption of the mitotic apparatus. This agent does not inhibit microtubule assembly in vitro, but does bind to tubulin. Molecular modelling of these structures indicates that their spatial and electronic structures may make an important contribution to the biological activity.

摘要

双(2-溴-4,5-二甲氧基苯基)硫醚(5)和双(2-溴-4,5-二甲氧基苯基)硒化物(7)已被证明可使细胞周期阻滞于G2/M期,而其脱溴类似物(4,6)则无此作用。生物溴硒化物(7)在体外对肿瘤细胞具有细胞毒性,并已证明可增加处理细胞的有丝分裂指数。这些生物学效应与有丝分裂装置的破坏一致。该药物在体外不抑制微管组装,但能与微管蛋白结合。这些结构的分子模拟表明,它们的空间和电子结构可能对生物活性有重要贡献。

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