Introduction of a terminal hydroxy group into the lipid part of a moenomycin-type transglycosylase inhibitor suppresses antibiotic activity-Reference-Cited by-同舟云学术

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Introduction of a terminal hydroxy group into the lipid part of a moenomycin-type transglycosylase inhibitor suppresses antibiotic activity

Published:1995-07 Issue:31 Volume:51 Page:8471-8482
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kempin Uwe,Hennig Lothar,Welzel Peter,Marzian Susanne,Müller Dietrich,Fehlhaber Hans-Wolfram,Markus Astrid,van Heijenoort Yveline,van Heijenoort Jean

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Bacterial Cell Wall,1994

2. A structurally and biogenetically interesting moenomycin antibiotic

3. The first synthesis of a moenomycin-type transglycosylase inhibitor

4. The first moenomycin antibiotic without the methyl-branched uronic acid constituent.- Unexpected structure activity relations

5. Structures of some moenomycin antibiotics - inhibitors of peptidoglycan biosynthesis

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2. Sesquiterpene Glycosides from Cosmospora joca;Journal of Natural Products;2011-06-17

3. Combinatorial approach toward synthesis of small molecule libraries as bacterial transglycosylase inhibitors;Organic & Biomolecular Chemistry;2010

4. Synthesis of moenocinol and its analogs using BT-sulfone in Julia-Kocienski olefination;Tetrahedron Letters;2007-02

5. Characterization of moenomycin antibiotic complex by multistage MALDI-IT/RTOF-MS and ESI-IT-MS;Journal of the American Society for Mass Spectrometry;2006-08-01

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