Alkaloids of thalictrum. XX. Isolation, identification and structural elucidation of the alkaloids of the root of Thalictrum longistylum.

Lloydia Pub Date : 1977-05-01
W N Wu, J L Beal, R P Leu, R W Doskotch
{"title":"Alkaloids of thalictrum. XX. Isolation, identification and structural elucidation of the alkaloids of the root of Thalictrum longistylum.","authors":"W N Wu,&nbsp;J L Beal,&nbsp;R P Leu,&nbsp;R W Doskotch","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>A study of the alkaloids of the roots of Thalictrum longistylum DC. resulted in the isolation of 12 alkaloids plus an artifact, 8-trichloromethyldihydroberberine. The 12 alkaloids were berberine, columbamine, jatrorrhizine, magnoflorine, methothalistyline, N-desmethylthalistyline, oxyberberine, palmatine, thalibrine, thalifendine, thaliglucinone, and thalistyline. Of these alkaloids, methothalistyline, N-desmethylthalistyline, and thalistyline are new compounds and with thaliglucinone possess hypotensive activity in dogs and rabbits. Methothalistyline, N-demethylthalistyline, thalistyline, and thalibrine were found to be active against Staphylococcus aureus and Mycobacterium smegmatis with with thalistyline being most active (50 microgram/ml).</p>","PeriodicalId":18256,"journal":{"name":"Lloydia","volume":"40 3","pages":"281-9"},"PeriodicalIF":0.0000,"publicationDate":"1977-05-01","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

A study of the alkaloids of the roots of Thalictrum longistylum DC. resulted in the isolation of 12 alkaloids plus an artifact, 8-trichloromethyldihydroberberine. The 12 alkaloids were berberine, columbamine, jatrorrhizine, magnoflorine, methothalistyline, N-desmethylthalistyline, oxyberberine, palmatine, thalibrine, thalifendine, thaliglucinone, and thalistyline. Of these alkaloids, methothalistyline, N-desmethylthalistyline, and thalistyline are new compounds and with thaliglucinone possess hypotensive activity in dogs and rabbits. Methothalistyline, N-demethylthalistyline, thalistyline, and thalibrine were found to be active against Staphylococcus aureus and Mycobacterium smegmatis with with thalistyline being most active (50 microgram/ml).

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
海芋生物碱。XX。长茎锥根生物碱的分离、鉴定及结构分析。
长茎锥根生物碱的研究。结果分离出12种生物碱和一种伪产物,8-三氯甲基二氢小檗碱。12种生物碱分别为小檗碱、柱状碱、麻草根碱、木兰碱、甲氧基苯乙胺、n -去甲基苯乙胺、oxyberberine、palmatine、thalinbrine、thalifendine、thaliglucinone和thalistyline。在这些生物碱中,methothalistyline、n -去甲基thalistyline和thalistyline是新化合物,它们与thaliglucinone一起对狗和兔子具有降血压的作用。Methothalistyline、N-demethylthalistyline、thalistyline和thalibrine对金黄色葡萄球菌和耻垢分枝杆菌均有活性,其中以thalistyline活性最强(50微克/毫升)。
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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