• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Microbial transformations of natural antitumor agents XXII: Conversion of bouvardin to O-desmethylbouvardin and bouvardin catechol.

作者信息

Petroski R J, Bates R B, Linz G S, Rosazza J P

出版信息

J Pharm Sci. 1983 Nov;72(11):1291-4. doi: 10.1002/jps.2600721114.

DOI:10.1002/jps.2600721114
PMID:6644590
Abstract

Bouvardin is a cyclic hexapeptide antitumor agent which undergoes two major microbial transformation reactions. Screening with 220 cultures revealed 17 different strains capable of producing O-desmethylbouvardin in good yield. O-Desmethylbouvardin was isolated and characterized from preparative scale incubations with Streptomyces rutgersensis NRRL B-1256. Four aspergilli and one streptomycete formed bouvardin catechol when O-desmethylbouvardin was used as substrate. Bouvardin catechol was isolated and characterized from a preparative scale incubation with Aspergillus ochraceous UI 398.

摘要

相似文献

1
Microbial transformations of natural antitumor agents XXII: Conversion of bouvardin to O-desmethylbouvardin and bouvardin catechol.
J Pharm Sci. 1983 Nov;72(11):1291-4. doi: 10.1002/jps.2600721114.
2
Microbial transformations of natural antitumor agents. 3. Conversion of thalicarpine to (+)-hernandalinol by Streptomyces punipalus.天然抗肿瘤药物的微生物转化。3. 普尼帕尔链霉菌将thalicarpine转化为(+)-hernandalinol。
J Med Chem. 1977 Jul;20(7):914-7. doi: 10.1021/jm00217a010.
3
Microbial transformations of natural antitumor agents. 7. 14-alpha-Hydroxylation of withaferin-A by Cunninghamella elegans (NRRL 1393).天然抗肿瘤药物的微生物转化。7. 雅致小克银汉霉(NRRL 1393)对睡茄素A的14-α-羟基化作用。
Steroids. 1978 May;31(5):671-9. doi: 10.1016/s0039-128x(78)80007-5.
4
Microbial transformations of natural antitumor agents. 23. Conversion of withaferin-A to 12 beta- and 15 beta-hydroxy derivatives of withaferin-A.
Steroids. 1982 Aug;40(2):157-69. doi: 10.1016/0039-128x(82)90030-7.
5
Fast atom bombardment mass spectrometry of bouvardin and selected analogs.波伐定及其选定类似物的快原子轰击质谱分析。
Biomed Mass Spectrom. 1985 Feb;12(2):72-8. doi: 10.1002/bms.1200120205.
6
Microbial transformations of natural antitumor agents: conversion of lapachol to dehydro-alpha-lapachone by Curvularia lunata.天然抗肿瘤药物的微生物转化:弯孢菌将拉帕醇转化为脱氢-α-拉帕醌
Appl Environ Microbiol. 1979 Aug;38(2):311-3. doi: 10.1128/aem.38.2.311-313.1979.
7
Microbial transformations of antitumor compounds. 1. Conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata.抗肿瘤化合物的微生物转化。1. 刺孢小克银汉霉将丙烯胺转化为9-羟基丙烯胺。
J Med Chem. 1974 Jun;17(6):599-602. doi: 10.1021/jm00252a006.
8
Microbial transformations of natural antitumor agents. VIII. Formation of 8- and 9-hydroxyellipticines.
Drug Metab Dispos. 1979 Jul-Aug;7(4):211-4.
9
Microbiological hydroxylation of estradiol: formation of 2- and 4-hydroxyestradiol by Aspergillus alliaceus.雌二醇的微生物羟基化作用:蒜曲霉生成2-羟基雌二醇和4-羟基雌二醇。
Appl Environ Microbiol. 1985 Mar;49(3):563-7. doi: 10.1128/aem.49.3.563-567.1985.
10
Reversal of natural resistance to bouvardin (NSC 259968) in sarcoma 180 cells in vitro and in vivo by verapamil.维拉帕米在体外和体内逆转肉瘤180细胞对布法地辛(NSC 259968)的天然耐药性。
J Cancer Res Clin Oncol. 1985;110(3):221-4. doi: 10.1007/BF00399277.