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膦甲酸及其他药物对HIV-1 RNA依赖性DNA聚合酶以及细胞DNA聚合酶α、β和γ的抑制作用。

Inhibition of HIV-1 RNA-dependent DNA polymerase and cellular DNA polymerases alpha, beta and gamma by phosphonoformic acid and other drugs.

作者信息

Wondrak E M, Löwer J, Kurth R

机构信息

Paul-Ehrlich-Institut, Frankfurt am Main, Federal Republic of Germany.

出版信息

J Antimicrob Chemother. 1988 Feb;21(2):151-61. doi: 10.1093/jac/21.2.151.

Abstract

Potential specific inhibitors of HIV RNA-dependent DNA polymerase (RDDP) were examined in an in-vitro test system containing purified HIV-1 RDDP, or functionally purified cellular DNA-dependent DNA polymerases alpha, beta and gamma. A wide variety of drugs were tested for their specific inhibitory activity against the viral enzyme to identify substances which, at the same concentration, did not inhibit the cellular DNA polymerases. Phosphonoformic acid and derivatives were found to be the most specific inhibitors, followed by chlortetracycline.

摘要

在一个包含纯化的HIV-1 RNA依赖性DNA聚合酶(RDDP)或功能纯化的细胞DNA依赖性DNA聚合酶α、β和γ的体外测试系统中,对HIV RNA依赖性DNA聚合酶(RDDP)的潜在特异性抑制剂进行了研究。测试了多种药物对病毒酶的特异性抑制活性,以鉴定在相同浓度下不抑制细胞DNA聚合酶的物质。发现膦甲酸及其衍生物是最具特异性的抑制剂,其次是金霉素。

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