• 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

揭示具有断裂 C 环的非典型蒽环类化合物的生物合成联系和功能。

Disclosing biosynthetic connections and functions of atypical angucyclinones with a fragmented C-ring.

机构信息

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 16/10 Miklukho-Maklaya St., Moscow, 117997, Russia.

出版信息

Nat Prod Rep. 2021 Aug 1;38(8):1506-1517. doi: 10.1039/d0np00082e. Epub 2021 Jan 22.

DOI:10.1039/d0np00082e
PMID:33480893
Abstract

This review on atypical angucyclinones possessing an aromatic cleavage of the C-ring covers literature between 1995 and early 2020.The unusual framework of the middle C-ring, "broken" as a result of biotransformations and oxidations in vivo and bearing an sp-C connection, is of interest for biosynthetic investigations. The reported 39 natural compounds (55 including stereoisomers) have been analyzed and arranged into three structural groups. The biosynthetic origin of all these compounds has been thoroughly reviewed and revised, based on the found connections with oxidized angucyclinone structures. The data on biological activities has been summarized. Careful consideration of the origin of the structure allowed us to outline a hypothesis on the biological function as well as prospective applications of such atypical angucyclinones.

摘要

这篇关于具有 C 环芳香裂解的非典型蒽环酮的综述涵盖了 1995 年至 2020 年初的文献。C 环中间结构的不寻常框架,由于体内的生物转化和氧化而“断裂”,并带有 sp-C 连接,这对于生物合成研究很有意义。报道的 39 种天然化合物(包括立体异构体在内的 55 种)已经进行了分析,并分为三个结构组。基于与氧化蒽环酮结构的发现联系,对所有这些化合物的生物合成起源进行了彻底的综述和修订。对生物活性数据进行了总结。对结构起源的仔细考虑使我们能够概述这种非典型蒽环酮的生物学功能以及潜在应用的假设。

相似文献

1
Disclosing biosynthetic connections and functions of atypical angucyclinones with a fragmented C-ring.揭示具有断裂 C 环的非典型蒽环类化合物的生物合成联系和功能。
Nat Prod Rep. 2021 Aug 1;38(8):1506-1517. doi: 10.1039/d0np00082e. Epub 2021 Jan 22.
2
Atypical Angucyclinones with Ring Expansion and Cleavage from a Marine sp.海洋来源 sp. 产生的具有环扩张和裂解的非典型蒽环酮类化合物
J Org Chem. 2022 Dec 2;87(23):15998-16010. doi: 10.1021/acs.joc.2c02134. Epub 2022 Nov 17.
3
Generation of Unusual Aromatic Polyketides by Incorporation of Phenylamine Analogues into a C-Ring-Cleaved Angucyclinone.通过将苯胺类似物掺入C环裂解的安古环素酮中生成不寻常的芳香族聚酮化合物。
Molecules. 2021 Mar 31;26(7):1959. doi: 10.3390/molecules26071959.
4
Discovery of a Phenylamine-Incorporated Angucyclinone from Marine Streptomyces sp. PKU-MA00218 and Generation of Derivatives with Phenylamine Analogues.从海洋链霉菌 sp. PKU-MA00218 中发现含苯氨基的蒽环酮类化合物及含苯氨基类似物衍生物的生成。
Org Lett. 2019 Apr 19;21(8):2813-2817. doi: 10.1021/acs.orglett.9b00800. Epub 2019 Mar 29.
5
Angucyclines and Angucyclinones from Streptomyces sp. CB01913 Featuring C-Ring Cleavage and Expansion.来自链霉菌属菌株CB01913的安古环素类和安古环酮类化合物,具有C环裂解和扩展特征。
J Nat Prod. 2015 Oct 23;78(10):2471-80. doi: 10.1021/acs.jnatprod.5b00601. Epub 2015 Sep 3.
6
Angucyclinones from an Indonesian Streptomyces sp.来自印度尼西亚链霉菌属的安古环素类化合物
J Nat Prod. 2008 Jan;71(1):61-5. doi: 10.1021/np0704102. Epub 2007 Dec 15.
7
Biosynthesis of Atypical Angucyclines Unveils New Ring Rearrangement Reactions Catalyzed by Flavoprotein Monooxygenases.非典型蒽环类化合物的生物合成揭示了黄素蛋白单加氧酶催化的新的环重排反应。
Org Lett. 2024 Sep 13;26(36):7489-7494. doi: 10.1021/acs.orglett.4c02074. Epub 2024 Aug 28.
8
Draft genome sequence of marine Streptomyces sp. strain W007, which produces angucyclinone antibiotics with a benz[a]anthracene skeleton.海洋链霉菌 W007 菌株的基因组草图,该菌株产生具有苯并[a]蒽骨架的安格环酮类抗生素。
J Bacteriol. 2012 Mar;194(6):1628-9. doi: 10.1128/JB.06701-11.
9
Antibacterial and Cytotoxic Bridged and Ring Cleavage Angucyclinones From a Marine sp.来自一种海洋物种的具有抗菌和细胞毒性的桥连及环裂解蒽环类化合物
Front Chem. 2020 Aug 4;8:586. doi: 10.3389/fchem.2020.00586. eCollection 2020.
10
[Novel angucycline/angucyclinone family of natural products discovered between 2010 and 2020].2010年至2020年间发现的新型蒽环类/蒽醌类天然产物家族
Sheng Wu Gong Cheng Xue Bao. 2021 Jun 25;37(6):2147-2165. doi: 10.13345/j.cjb.210033.

引用本文的文献

1
Divergence of Classical and C-Ring-Cleaved Angucyclines: Elucidation of Early Tailoring Steps in Lugdunomycin and Thioangucycline Biosynthesis.经典型与 C 环断裂安卡霉素类的差异:卢格多霉素和硫杂安卡霉素生物合成中早期修饰步骤的阐明。
ACS Chem Biol. 2024 May 17;19(5):1131-1141. doi: 10.1021/acschembio.4c00082. Epub 2024 Apr 26.
2
Unravelling key enzymatic steps in C-ring cleavage during angucycline biosynthesis.解析安古霉素生物合成过程中C环裂解的关键酶促步骤。
Commun Chem. 2023 Dec 18;6(1):281. doi: 10.1038/s42004-023-01059-1.
3
Racemic Total Synthesis of Elmonin and Pratenone A, from , Using a Common Intermediate Prepared by -Directed C-H Functionalization.
(-)-埃洛莫宁和普拉替酮 A 的外消旋全合成,来自 ,使用 -定向 C-H 功能化制备的共同中间体。
Org Lett. 2022 Dec 30;24(51):9361-9365. doi: 10.1021/acs.orglett.2c03449. Epub 2022 Dec 19.