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DNA聚合酶γ和逆转录酶对ara-UTP的5-卤代衍生物结构的识别。

Recognition of structure of 5-halogenated derivatives of ara-UTP by DNA polymerase gamma and reverse transcriptase.

作者信息

Ono K, Ogasawara M, Ohashi A, Matsukage A, Takahashi T, Nakayama C, Saneyoshi M

出版信息

Nucleic Acids Symp Ser. 1979(6):s129-32.

PMID:94943
Abstract

This report deals with the test of a series of 5-halogenated derivatives of ara-UTP for the inhibition of DNA polymerase gamma and viral reverse transcriptase. The compounds newly synthesized and tested were; ara5-FUTP, ara5-C1UTP, ara5-BrUTP and ara5-IUTP. The results were: 1) All these compounds were inhibitory to DNA polymerase gamma and reverse transcriptase. The mode of inhibitions was, in all cases, competitive against dTTP. 2) Ki values for these inhibitors with DNA polymerase gamma were lower than those with reverse transcriptase. 3) Ara5-ClUTP was less inhibitory to reverse transcriptase than other derivatives.

摘要

本报告涉及一系列5-卤代阿糖胞苷三磷酸(ara-UTP)衍生物对DNA聚合酶γ和病毒逆转录酶抑制作用的测试。新合成并测试的化合物有:5-氟阿糖胞苷三磷酸(ara5-FUTP)、5-氯阿糖胞苷三磷酸(ara5-C1UTP)、5-溴阿糖胞苷三磷酸(ara5-BrUTP)和5-碘阿糖胞苷三磷酸(ara5-IUTP)。结果如下:1)所有这些化合物均对DNA聚合酶γ和逆转录酶有抑制作用。在所有情况下,抑制模式均为与脱氧胸苷三磷酸(dTTP)竞争。2)这些抑制剂对DNA聚合酶γ的抑制常数(Ki)值低于对逆转录酶的抑制常数。3)5-氯阿糖胞苷三磷酸(ara5-ClUTP)对逆转录酶的抑制作用比其他衍生物弱。

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