INHIBITION OF REVERSE-TRANSCRIPTASE ACTIVITY BY BENZOPHENANTHRIDINE ALKALOIDS

被引:31
作者
SETHI, ML
机构
[1] Department of Biomedicinal Chemistry, College of Pharmacy and Pharmacol Sciences, Howard University, Washington
来源
LLOYDIA-THE JOURNAL OF NATURAL PRODUCTS | 1979年 / 42卷 / 02期
关键词
D O I
10.1021/np50002a010
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
Benzophenanthridine alkaloids, fagaronine 4, O-methylfagaronine 5, nitidine 1, allonitidine 3 and methoxydihydronitidine 2 have been shown to possess inhibitory activity against reverse transcriptase of RNA tumor viruses. The enzyme inhibition (50%) by these alkaloids was found in the range of 6-60μg per milliliter of the reaction mixture when polynucleotide-oligodeoxynucleotide complexes were used as template primers. The results suggested that the benzophenanthridine alkaloids interacted with the template primers (particularly of the A:T base pairs) and not with the enzyme proteins. Kinetics reaction of the reverse transciptase inhibition showed that the alkaloids stopped the DNA polymerase synthesis instantly, probably by interacting with the template primer. © 1979, American Chemical Society. All rights reserved.
引用
收藏
页码:187 / 196
页数:10
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