• 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

10'-去甲氧基链黑菌素,链黑菌素的一种新型类似物。

10'-Desmethoxystreptonigrin, a novel analog of streptonigrin.

作者信息

Liu W C, Barbacid M, Bulgar M, Clark J M, Crosswell A R, Dean L, Doyle T W, Fernandes P B, Huang S, Manne V

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000.

出版信息

J Antibiot (Tokyo). 1992 Apr;45(4):454-7. doi: 10.7164/antibiotics.45.454.

DOI:10.7164/antibiotics.45.454
PMID:1592677
Abstract

10'-Desmethoxystreptonigrin, a novel analog of streptonigrin produced by Streptomyces albus, was discovered in a screen for inhibitors of farnesylation of RAS p21 protein. The compound was isolated from the fermentation broth and its structure determined. It is markedly cytotoxic to several human tumor cell lines and also exhibits potent broad-spectrum antibacterial activity.

摘要

10'-去甲氧基链黑菌素是由白色链霉菌产生的链黑菌素的一种新型类似物,它是在筛选RAS p21蛋白法尼基化抑制剂时发现的。该化合物从发酵液中分离出来并确定了其结构。它对几种人类肿瘤细胞系具有显著的细胞毒性,并且还表现出强大的广谱抗菌活性。

相似文献

1
10'-Desmethoxystreptonigrin, a novel analog of streptonigrin.10'-去甲氧基链黑菌素,链黑菌素的一种新型类似物。
J Antibiot (Tokyo). 1992 Apr;45(4):454-7. doi: 10.7164/antibiotics.45.454.
2
Isolation of lavendamycin, a new antibiotic from Streptomyces lavendulae.
J Antibiot (Tokyo). 1982 Mar;35(3):259-65. doi: 10.7164/antibiotics.35.259.
3
C-1027 enediyne chromophore: presence of another active form and its chemical structure.C-1027烯二炔发色团:另一种活性形式的存在及其化学结构。
J Antibiot (Tokyo). 1999 Apr;52(4):415-21. doi: 10.7164/antibiotics.52.415.
4
Novel cytocidal compounds, oxopropalines from Streptomyces sp. G324 producing lavendamycin. I. Taxonomy of the producing organism, fermentation, isolation and biological activities.新型杀细胞化合物,来自产生薰衣草霉素的链霉菌属G324的氧代丙氨酸。I. 产生菌的分类学、发酵、分离及生物活性
J Antibiot (Tokyo). 1993 Nov;46(11):1672-7. doi: 10.7164/antibiotics.46.1672.
5
Chrolactomycin, a novel antitumor antibiotic produced by Streptomyces sp.氯乳霉素,一种由链霉菌属产生的新型抗肿瘤抗生素。
J Antibiot (Tokyo). 2001 Oct;54(10):836-9. doi: 10.7164/antibiotics.54.836.
6
Manumycins E, F and G, new members of manumycin class antibiotics, from Streptomyces sp.来自链霉菌属的马尼霉素类抗生素新成员马尼霉素E、F和G
J Antibiot (Tokyo). 1994 Mar;47(3):324-33. doi: 10.7164/antibiotics.47.324.
7
A new antitumor antibiotic: demethylstreptonigrin.
J Antibiot (Tokyo). 1986 Jul;39(7):1013-5. doi: 10.7164/antibiotics.39.1013.
8
RK-397, a new oxo pentaene antibiotic.RK - 397,一种新型氧代戊二烯抗生素。
J Antibiot (Tokyo). 1993 Oct;46(10):1616-8. doi: 10.7164/antibiotics.46.1616.
9
Novel cytocidal compounds, oxopropalines from Streptomyces sp. G324 producing lavendamycin. II. Physico-chemical properties and structure elucidations.新型杀细胞化合物,来自产生薰衣草霉素的链霉菌属G324的氧代丙氨酸。II. 物理化学性质及结构解析。
J Antibiot (Tokyo). 1993 Nov;46(11):1678-86. doi: 10.7164/antibiotics.46.1678.
10
Novel antitumor antibiotics, saptomycins D and E.
J Antibiot (Tokyo). 1991 Aug;44(8):908-11. doi: 10.7164/antibiotics.44.908.

引用本文的文献

1
Chaetomella acutiseta produces chaetomellic acids A and B which are reversible inhibitors of farnesyl-protein transferase.尖锐毛壳菌产生毛壳菌素A和B,它们是法尼基蛋白转移酶的可逆抑制剂。
Appl Microbiol Biotechnol. 1993 Nov;40(2-3):370-4. doi: 10.1007/BF00170395.
2
Actinoplanic acids A and B as novel inhibitors of farnesyl-protein transferase.放线菌酸A和B作为法尼基蛋白转移酶的新型抑制剂。
Appl Microbiol Biotechnol. 1995 Aug-Sep;43(4):610-6. doi: 10.1007/BF00164762.