• 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

TAN-1120, a new anthracycline with potent angiostatic activity.

作者信息

Nozaki Y, Hida T, Iinuma S, Ishii T, Sudo K, Muroi M, Kanamaru T

机构信息

Discovery Research Division, Takeda Chemical Industries, Ltd., Osaka, Japan.

出版信息

J Antibiot (Tokyo). 1993 Apr;46(4):569-79. doi: 10.7164/antibiotics.46.569.

DOI:10.7164/antibiotics.46.569
PMID:7684735
Abstract

A potent angiogenesis-inhibitory compound TAN-1120 was found to be produced by a Streptomyces species isolated from a soil sample. The producing organism was characterized as a new subspecies of S. triangulatus and named S. triangulatus subsp. angiostaticus subsp. nov. due to its specific ability to produce the compound. This substance was isolated as a red powder by a combination of organic solvent extraction, silica gel column chromatography and preparative HPLC using an ODS column. Its structure was elucidated by chemical reactions and spectral analyses to be a new baumycin-group anthracycline. Reduction of TAN-1120 gave two compounds, a deoxy derivative and baumycin A1. TAN-1120 showed remarkably potent angiostatic activity in two conventional angiogenesis assay systems in vivo, while doxorubicin and daunomycin had far weaker activity. It strongly inhibited proliferation of vascular endothelial cells did not prevent capillary cord formation in vitro by the endothelial cells on extracellular matrix-coated plates. TAN-1120 is one of the most potent angiostatic agents reported.

摘要

相似文献

1
TAN-1120, a new anthracycline with potent angiostatic activity.
J Antibiot (Tokyo). 1993 Apr;46(4):569-79. doi: 10.7164/antibiotics.46.569.
2
Respinomycins A1, A2 B, C and D, a novel group of anthracycline antibiotics. I. Taxonomy, fermentation, isolation and biological activities.
J Antibiot (Tokyo). 1993 Jun;46(6):936-41. doi: 10.7164/antibiotics.46.936.
3
A new anthracycline antibiotic, IT-62-B, converts the morphology of ras-transformed cells back to normal: taxonomy, fermentation, isolation, structure elucidation and biological characterization.一种新的蒽环类抗生素IT-62-B可使经ras基因转化的细胞形态恢复正常:分类学、发酵、分离、结构解析及生物学特性研究。
J Antibiot (Tokyo). 1997 Apr;50(4):297-303. doi: 10.7164/antibiotics.50.297.
4
TAN-1323 C and D, new concanamycin-group antibiotics; detection of the angiostatic activity with a wide range of macrolide antibiotics.TAN-1323 C和D,新型刀豆氨酸类抗生素;多种大环内酯类抗生素血管生成抑制活性的检测
J Antibiot (Tokyo). 1995 Jan;48(1):12-20. doi: 10.7164/antibiotics.48.12.
5
A new anthracycline antibiotic, cinerubin R. Taxonomy, structural elucidation and biological activity.一种新的蒽环类抗生素,烬灰红菌素R。分类学、结构解析及生物活性。
J Antibiot (Tokyo). 1992 Oct;45(10):1599-608. doi: 10.7164/antibiotics.45.1599.
6
Anthracycline metabolites from Streptomyces violaceus A262. II. New anthracycline epelmycins produced by a blocked mutant strain SU2-730.来自紫色链霉菌A262的蒽环类代谢产物。II. 由阻断突变株SU2-730产生的新型蒽环类埃佩霉素
J Antibiot (Tokyo). 1991 Oct;44(10):1121-9. doi: 10.7164/antibiotics.44.1121.
7
Anthracycline metabolites from Streptomyces violaceus A262. III. New anthracycline obelmycins produced by a variant strain SE2-2385.来自紫色链霉菌A262的蒽环类代谢产物。III. 变异菌株SE2-2385产生的新型蒽环类奥贝霉素
J Antibiot (Tokyo). 1991 Oct;44(10):1130-40. doi: 10.7164/antibiotics.44.1130.
8
Anthracycline metabolites from baumycin-producing Streptomyces sp. D788. II. New anthracycline metabolites produced by a blocked mutant strain RPM-5.
J Antibiot (Tokyo). 1993 Jan;46(1):56-64. doi: 10.7164/antibiotics.46.56.
9
Anthracycline metabolites from Streptomyces violaceus A262. V. New anthracycline alldimycin A: a minor component isolated from obelmycin beer.
J Antibiot (Tokyo). 1991 Oct;44(10):1160-4. doi: 10.7164/antibiotics.44.1160.
10
Anthracycline metabolites from Streptomyces violaceus A262. IV. New anthracycline yellamycins produced by a variant strain SC-7.
J Antibiot (Tokyo). 1991 Oct;44(10):1155-9. doi: 10.7164/antibiotics.44.1155.

引用本文的文献

1
Discovery of human cell selective effector molecules using single cell multiplexed activity metabolomics.利用单细胞多重活性代谢组学发现人类细胞选择性效应分子。
Nat Commun. 2018 Jan 2;9(1):39. doi: 10.1038/s41467-017-02470-8.
2
The Chick Embryo Chorioallantoic Membrane as an In Vivo Assay to Study Antiangiogenesis.鸡胚绒毛尿囊膜作为一种研究抗血管生成的体内检测方法。
Pharmaceuticals (Basel). 2010 Mar 8;3(3):482-513. doi: 10.3390/ph3030482.
3
A new cyano-substituted anthracycline metabolite from Streptomyces sp. HS-NF-1006.一种来自链霉菌属HS-NF-1006的新型氰基取代蒽环类代谢产物。
J Antibiot (Tokyo). 2017 Feb;70(2):219-221. doi: 10.1038/ja.2016.112. Epub 2016 Sep 7.
4
Nitrososynthase-triggered oxidative carbon-carbon bond cleavage in baumycin biosynthesis.硝硫基合酶触发巴龙霉素生物合成中的氧化碳-碳键断裂。
J Am Chem Soc. 2013 Aug 7;135(31):11457-60. doi: 10.1021/ja404987r. Epub 2013 Jul 25.
5
Neomycin inhibits angiogenin-induced angiogenesis.新霉素抑制血管生成素诱导的血管生成。
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9791-5. doi: 10.1073/pnas.95.17.9791.
6
Antitumor effect of arterial administration of a medium-chain triglyceride solution of an angiogenesis inhibitor, TNP-470, in rabbits bearing VX-2 carcinoma.血管生成抑制剂TNP - 470的中链甘油三酯溶液动脉给药对荷VX - 2癌兔的抗肿瘤作用
Pharm Res. 1995 May;12(5):653-7. doi: 10.1023/a:1016243105622.