• 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

由链霉菌属菌株K01-0509产生的III型分泌系统抑制剂古地诺霉素。II:物理化学性质及结构解析

Guadinomines, Type III secretion system inhibitors, produced by Streptomyces sp. K01-0509. II: physico-chemical properties and structure elucidation.

作者信息

Iwatsuki Masato, Uchida Ryuji, Yoshijima Hitomi, Ui Hideaki, Shiomi Kazuro, Kim Yong-Pil, Hirose Tomoyasu, Sunazuka Toshiaki, Abe Akio, Tomoda Hiroshi, Omura Satoshi

机构信息

The Kitasato Institute, Japan.

出版信息

J Antibiot (Tokyo). 2008 Apr;61(4):230-6. doi: 10.1038/ja.2008.33.

DOI:10.1038/ja.2008.33
PMID:18503202
Abstract

The structures of guadinomines, new inhibitors of a bacterial Type III secretion system produced by Streptomyces sp. K01-0509, were elucidated by spectroscopic studies including various NMR experiments. Guadinomines A, B, C(1), C(2) and D consist of a carbamoylated cyclic guanidinyl moiety, an alkyl chain moiety and an L-Ala-L-Val moiety in common, while guadinomic acid is a smaller molecule consisting of a carbamoylated cyclic guanidinyl moiety and a hydroxyl hexanoate moiety.

摘要

胍迪诺霉素是由链霉菌属菌株K01 - 0509产生的一种新型细菌III型分泌系统抑制剂,通过包括各种核磁共振实验在内的光谱学研究阐明了其结构。胍迪诺霉素A、B、C(1)、C(2)和D共同由一个氨甲酰化的环状胍基部分、一个烷基链部分和一个L - 丙氨酰 - L - 缬氨酸部分组成,而胍迪诺酸是一个较小的分子,由一个氨甲酰化的环状胍基部分和一个羟基己酸部分组成。

相似文献

1
Guadinomines, Type III secretion system inhibitors, produced by Streptomyces sp. K01-0509. II: physico-chemical properties and structure elucidation.由链霉菌属菌株K01-0509产生的III型分泌系统抑制剂古地诺霉素。II:物理化学性质及结构解析
J Antibiot (Tokyo). 2008 Apr;61(4):230-6. doi: 10.1038/ja.2008.33.
2
Guadinomines, Type III secretion system inhibitors, produced by Streptomyces sp. K01-0509. I: taxonomy, fermentation, isolation and biological properties.由链霉菌属菌株K01-0509产生的III型分泌系统抑制剂古地诺霉素。I:分类学、发酵、分离及生物学特性。
J Antibiot (Tokyo). 2008 Apr;61(4):222-9. doi: 10.1038/ja.2008.32.
3
A-94964, novel inhibitor of bacterial translocase I, produced by Streptomyces sp. SANK 60404. II. Physico-chemical properties and structure elucidation.链霉菌SANK 60404产生的新型细菌转位酶I抑制剂A-94964。II. 理化性质及结构解析
J Antibiot (Tokyo). 2008 Sep;61(9):545-9. doi: 10.1038/ja.2008.72.
4
Nosokomycins, new antibiotics discovered in an in vivo-mimic infection model using silkworm larvae. II: Structure elucidation.蚕幼虫体内模拟感染模型中发现的新抗生素 Nosokomycins。II:结构阐明。
J Antibiot (Tokyo). 2010 Apr;63(4):157-63. doi: 10.1038/ja.2010.10. Epub 2010 Mar 5.
5
Total synthesis and determination of the absolute configuration of guadinomines B and C2.胍地诺明B和C2的全合成及绝对构型的确定
Chemistry. 2008;14(27):8220-38. doi: 10.1002/chem.200801024.
6
Molecular insights into the biosynthesis of guadinomine: a type III secretion system inhibitor.胍丁胺生物合成的分子机制研究:一种 III 型分泌系统抑制剂。
J Am Chem Soc. 2012 Oct 24;134(42):17797-806. doi: 10.1021/ja308622d. Epub 2012 Oct 10.
7
A novel isoquinoline alkaloid, DD-carboxypeptidase inhibitor, with antibacterial activity isolated from Streptomyces sp. 8812. Part II: Physicochemical properties and structure elucidation.
J Antibiot (Tokyo). 2009 Oct;62(10):581-5. doi: 10.1038/ja.2009.86. Epub 2009 Aug 28.
8
Lariatins, antimycobacterial peptides produced by Rhodococcus sp. K01-B0171, have a lasso structure.拉瑞菌素是红球菌属K01 - B0171产生的抗分枝杆菌肽,具有套索结构。
J Am Chem Soc. 2006 Jun 14;128(23):7486-91. doi: 10.1021/ja056780z.
9
Cyslabdan, a new potentiator of imipenem activity against methicillin-resistant Staphylococcus aureus, produced by Streptomyces sp. K04-0144. I. Taxonomy, fermentation, isolation and structural elucidation.Cyslabdan,一种由链霉菌属K04 - 0144产生的新型亚胺培南抗耐甲氧西林金黄色葡萄球菌活性增强剂。I. 分类学、发酵、分离及结构解析。
J Antibiot (Tokyo). 2008 Jan;61(1):1-6. doi: 10.1038/ja.2008.101.
10
NW-G01, a novel cyclic hexapeptide antibiotic, produced by Streptomyces alboflavus 313: II. Structural elucidation.新型环六肽抗生素 NW-G01,由白色链霉菌 313 产生:Ⅱ.结构解析。
J Antibiot (Tokyo). 2010 May;63(5):231-5. doi: 10.1038/ja.2010.24. Epub 2010 Apr 9.

引用本文的文献

1
Fighting Antimicrobial Resistance: Innovative Drugs in Antibacterial Research.对抗抗菌药物耐药性:抗菌研究中的创新药物
Angew Chem Int Ed Engl. 2025 Mar 3;64(10):e202414325. doi: 10.1002/anie.202414325. Epub 2025 Feb 10.
2
PurA is the main target of aurodox, a type III secretion system inhibitor.PurA 是一种 III 型分泌系统抑制剂aurodox 的主要靶标。
Proc Natl Acad Sci U S A. 2024 Apr 23;121(17):e2322363121. doi: 10.1073/pnas.2322363121. Epub 2024 Apr 19.
3
Targeting bacterial pathogenesis by inhibiting virulence-associated Type III and Type IV secretion systems.
通过抑制与毒力相关的 III 型和 IV 型分泌系统来靶向细菌发病机制。
Front Cell Infect Microbiol. 2023 Jan 10;12:1065561. doi: 10.3389/fcimb.2022.1065561. eCollection 2022.
4
Research Progress on Small Molecular Inhibitors of the Type 3 Secretion System.III 型分泌系统小分子抑制剂的研究进展。
Molecules. 2022 Nov 30;27(23):8348. doi: 10.3390/molecules27238348.
5
Natural Product Type III Secretion System Inhibitors.天然产物Ⅲ型分泌系统抑制剂
Antibiotics (Basel). 2019 Sep 24;8(4):162. doi: 10.3390/antibiotics8040162.
6
Total Synthesis of (+)-Guadinomic Acid via Hydroxyl-Directed Guanidylation.通过羟基导向胍基化的 (+)-瓜环酸的全合成。
J Org Chem. 2018 Aug 17;83(16):9492-9496. doi: 10.1021/acs.joc.8b01214. Epub 2018 Jun 22.
7
Stereoselective Synthesis of Isoxazolidines via Copper-Catalyzed Alkene Diamination.通过铜催化的烯烃双胺化反应立体选择性合成异恶唑烷。
ACS Catal. 2017 Jul 7;7(7):4775-4779. doi: 10.1021/acscatal.7b01362. Epub 2017 Jun 15.
8
Cladomarine, a new anti-saprolegniasis compound isolated from the deep-sea fungus, Penicillium coralligerum YK-247.枝状海菌素,一种从深海真菌珊瑚状青霉YK-247中分离出的新型抗水霉病化合物。
J Antibiot (Tokyo). 2017 Jul;70(8):911-914. doi: 10.1038/ja.2017.58. Epub 2017 May 31.
9
Streptomyces Bacteria as Potential Probiotics in Aquaculture.链霉菌作为水产养殖中潜在的益生菌
Front Microbiol. 2016 Feb 5;7:79. doi: 10.3389/fmicb.2016.00079. eCollection 2016.
10
Small-Molecule Inhibitors of the Type III Secretion System.III型分泌系统的小分子抑制剂
Molecules. 2015 Sep 23;20(9):17659-74. doi: 10.3390/molecules200917659.