Literature DB >> 21868221

Hydrazidomycins, cytotoxic alkylhydrazides from Streptomycesatratus.

Nico Ueberschaar1, Basile Le Sage Tchize Ndejouong, Ling Ding, Armin Maier, Heinz-Herbert Fiebig, Christian Hertweck.   

Abstract

Three unusual alkyhydrazide natural products, named hydrazidomycin A (1), B (2) and C (3), were isolated from the chloroform extract of a Streptomycesatratus culture, and their structures were elucidated by MS and NMR techniques. Hydrazidomycins A-C exhibited moderate to strong cytotoxic activities in a panel of 42 cell lines, with hydrazidomycin A being the most potent compound (mean IC(50)=0.37 μM).
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21868221     DOI: 10.1016/j.bmcl.2011.07.108

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  Novel ynamide structural analogues and their synthetic transformations.

Authors:  Ting Lu; Richard P Hsung
Journal:  ARKIVOC       Date:  2014       Impact factor: 1.140

2.  The diversity of bacterial endophytes from Iris pseudacorus L. and their plant beneficial traits.

Authors:  Vyacheslav Shurigin; Jakhongir Alimov; Kakhramon Davranov; Tashkhan Gulyamova; Dilfuza Egamberdieva
Journal:  Curr Res Microb Sci       Date:  2022-04-12

3.  Discovery of a New Natural Product and a Deactivation of a Quorum Sensing System by Culturing a "Producer" Bacterium With a Heat-Killed "Inducer" Culture.

Authors:  Libang Liang; Amanda Sproule; Brad Haltli; Douglas H Marchbank; Fabrice Berrué; David P Overy; Kate McQuillan; Martin Lanteigne; Noelle Duncan; Hebelin Correa; Russell G Kerr
Journal:  Front Microbiol       Date:  2019-01-17       Impact factor: 5.640

  3 in total

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