Inhibition of reverse transcriptase activity by benzophenanthridine alkaloids.

Lloydia Pub Date : 1979-03-01
M L Sethi
{"title":"Inhibition of reverse transcriptase activity by benzophenanthridine alkaloids.","authors":"M L Sethi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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 6-60 microgram 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.</p>","PeriodicalId":18256,"journal":{"name":"Lloydia","volume":"42 2","pages":"187-96"},"PeriodicalIF":0.0000,"publicationDate":"1979-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lloydia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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 6-60 microgram 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.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
苯并苯胺生物碱对逆转录酶活性的抑制作用。
苯并苯胺类生物碱、fagaronine 4、o -甲基fagaronine 5、nitidine 1、allonitidine 3和methoxydihydronitidine 2对RNA肿瘤病毒的逆转录酶具有抑制活性。当多核苷酸-寡脱氧核苷酸复合物作为模板引物时,这些生物碱对酶的抑制作用为6-60微克/毫升。结果表明,苯并苯胺生物碱与模板引物(特别是A:T碱基对)相互作用,而不与酶蛋白相互作用。反转录酶抑制的动力学反应表明,生物碱可能与模板引物相互作用,使DNA聚合酶的合成瞬间停止。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Plants used against cancer. A survey. Inhibition of reverse transcriptase activity by benzophenanthridine alkaloids. (+)Nortrachelogenin, a new pharmacologically active lignan from Wikstroemia indica. Proceedings of the 19th Annual Meeting of the American Society of Pharmacognosy held with the Phytochemical Society of North America, August 14-17, 1978, Oklahoma State University, Stillwater, Oklahoma. Plant antitumor agents. XVI. 6alpha-Senecioyloxy-chaparrinone, a new antileukemic quassinoid from Simaba multiflora.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1