Conversion of a Disulfide Bond into a Thioacetal Group during Echinomycin Biosynthesis-Reference-Cited by-同舟云学术

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Conversion of a Disulfide Bond into a Thioacetal Group during Echinomycin Biosynthesis

Published:2013-12-02 Issue:3 Volume:126 Page:843-847
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Hotta Kinya,Keegan Ronan M.,Ranganathan Soumya,Fang Minyi,Bibby Jaclyn,Winn Martyn D.,Sato Michio,Lian Mingzhu,Watanabe Kenji,Rigden Daniel J.,Kim Chu-Young

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201307404/fullpdf

Reference26 articles.

1. Total Syntheses of Thiocoraline and BE-22179 and Assessment of Their DNA Binding and Biological Properties

2. Thiocoraline, a New Depsipeptide with Antitumor Activity Produced by a Marine Micromonospora. I. Taxonomy, Fermentation, Isolation, and Biological Activities.

3. The role of the cyclic depsipeptide rings in antibiotics.

4. Quinaldopeptin, a novel antibiotic of the quinomycin family.

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bacteria Hunt Bacteria through an Intriguing Cyclic Peptide;ChemMedChem;2018-12-10

2. A Vastly Increased Chemical Variety of RNA Modifications Containing a Thioacetal Structure;Angewandte Chemie International Edition;2018-04-27

3. Die stark wachsende chemische Vielfalt der RNA-Modifikationen enthält eine Thioacetalstruktur;Angewandte Chemie;2018-04-27

4. Enzyme from an Uncultivated Sponge Bacterium Catalyzes S-Methylation in a Ribosomal Peptide;ChemBioChem;2017-01-20

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