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首页> 外文期刊>Biochemical Pharmacology >4-Hydroxy-17-methylincisterol, an inhibitor of DNA polymerase-alpha activity and the growth of human cancer cells in vitro.
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4-Hydroxy-17-methylincisterol, an inhibitor of DNA polymerase-alpha activity and the growth of human cancer cells in vitro.

机译:4-Hydroxy-17-methylincisterol,一种DNA聚合酶α活性和体外人类癌细胞生长的抑制剂。

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摘要

An ergosterol derivative, 4-hydroxy-17-methylincisterol (HMI), was found to be an inhibitor of mammalian DNA polymerases in vitro. HMI inhibited the activity of calf thymus DNA polymerase alpha (pol. alpha). Among the polymerases tested, pol. alpha was the most sensitive to inhibition by HMI, and the inhibition was concentration dependent. The inhibitory effect of HMI on pol. alpha was almost the same as that shown by aphidicolin, a well-known potent pol. alpha inhibitor. HMI had relatively less effect on rat DNA pol. beta, human immunodeficiency virus type 1 reverse transcriptase (HIV-RT), and calf thymus terminal deoxynucleotidyl transferase (TdT) in vitro, and did not influence the activities of prokaryotic DNA polymerases such as Klenow Fragment of DNA polymerase I, or the DNA-metabolic enzyme DNase I. HMI was found to be able to prevent the growth of human cancer cell lines originating from patients with leukemia or various solid tumors; its IC50 values ranged from 7.5 to 12 microM. We also synthesized other ergosterol derivatives and tested them, and found that two compounds, 17-methylincisterol and 4-acetyl-17-methylincisterol, have similar inhibitory effects.
机译:发现麦角固醇衍生物4-羟基-17-甲基incincisterol(HMI)是体外哺乳动物DNA聚合酶的抑制剂。 HMI抑制小牛胸腺DNA聚合酶α(pol。alpha)的活性。在测试的聚合酶中,pol。 α对HMI的抑制作用最敏感,抑制作用与浓度有关。 HMI对pol的抑制作用。 α几乎与著名的强效蚜虫Aphidicolin所显示的相同。 α抑制剂。 HMI对大鼠DNA pol的影响相对较小。 β,1型人类免疫缺陷病毒逆转录酶(HIV-RT)和小牛胸腺末端脱氧核苷酸转移酶(TdT),并且不影响原核DNA聚合酶的活性,例如DNA聚合酶I的Klenow片段或DNA-代谢酶DNase I. HMI被发现能够预防源自白血病或各种实体瘤患者的人类癌细胞系的生长;其IC50值范围为7.5至12 microM。我们还合成了其他麦角固醇衍生物并对其进行了测试,发现两种化合物17-甲基incisterol和4-acetyl-17-methylincisterol具有相似的抑制作用。

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