Brinkworth R I, Stoermer M J, Fairlie D P
Centre for Drug Design and Development, University of Queensland, Brisbane, Australia.
Biochem Biophys Res Commun. 1992 Oct 30;188(2):631-7. doi: 10.1016/0006-291x(92)91103-w.
Substituted gamma-chromones were found to weakly inhibit HIV-1 proteinase, an important enzyme in the replication and processing of the AIDS virus. Chromones bearing hydroxyl substituents and a phenolic group at the 2-position (flavones) were the most active compounds and structure-activity relationships for a limited series of flavone inhibitors are presented. Dixon plots are reported and a possible mechanism for flavone-induced inhibition is proposed. The results are also compared with those for some structurally related non-peptidic inhibitors of HIV-1 proteinase. Since some flavonoid compounds have already been shown to have antiviral activity against AIDS, the present observations of anti-HIV-1 proteinase activity may be particularly significant.
已发现取代的γ-色酮可微弱抑制HIV-1蛋白酶,这是一种在艾滋病病毒复制和加工过程中起重要作用的酶。在2-位带有羟基取代基和酚羟基的色酮(黄酮)是最具活性的化合物,并给出了一系列有限的黄酮抑制剂的构效关系。报告了 Dixon 图,并提出了黄酮诱导抑制的可能机制。还将结果与一些结构相关的HIV-1蛋白酶非肽类抑制剂的结果进行了比较。由于一些黄酮类化合物已被证明对艾滋病具有抗病毒活性,因此目前关于抗HIV-1蛋白酶活性的观察结果可能特别重要。