FLAVONES ARE INHIBITORS OF HIV-1 PROTEINASE

被引:108
作者
BRINKWORTH, RI [1 ]
STOERMER, MJ [1 ]
FAIRLIE, DP [1 ]
机构
[1] UNIV QUEENSLAND,CTR DRUG DESIGN & DEV,BRISBANE,QLD 4072,AUSTRALIA
关键词
D O I
10.1016/0006-291X(92)91103-W
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Substituted γ-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. © 1992.
引用
收藏
页码:631 / 637
页数:7
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