Cargando…

Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila

The repeated and improper use of antibiotics had led to an increased number of multiresistant bacteria. Therefore, new lead structures are needed. Here, the synthesis and an expanded structure–activity relationship of the simple and antistaphylococcal amide nematophin from Xenorhabdus nematophila an...

Descripción completa

Detalles Bibliográficos
Autores principales: Wesche, Frank, Adihou, Hélène, Wichelhaus, Thomas A, Bode, Helge B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404511/
https://www.ncbi.nlm.nih.gov/pubmed/30873237
http://dx.doi.org/10.3762/bjoc.15.47
_version_ 1783400907110612992
author Wesche, Frank
Adihou, Hélène
Wichelhaus, Thomas A
Bode, Helge B
author_facet Wesche, Frank
Adihou, Hélène
Wichelhaus, Thomas A
Bode, Helge B
author_sort Wesche, Frank
collection PubMed
description The repeated and improper use of antibiotics had led to an increased number of multiresistant bacteria. Therefore, new lead structures are needed. Here, the synthesis and an expanded structure–activity relationship of the simple and antistaphylococcal amide nematophin from Xenorhabdus nematophila and synthetic derivatives are described. Moreover, the synthesis of intrinsic fluorescent derivatives, incorporating azaindole moieties was achieved for the first time.
format Online
Article
Text
id pubmed-6404511
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-64045112019-03-14 Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila Wesche, Frank Adihou, Hélène Wichelhaus, Thomas A Bode, Helge B Beilstein J Org Chem Full Research Paper The repeated and improper use of antibiotics had led to an increased number of multiresistant bacteria. Therefore, new lead structures are needed. Here, the synthesis and an expanded structure–activity relationship of the simple and antistaphylococcal amide nematophin from Xenorhabdus nematophila and synthetic derivatives are described. Moreover, the synthesis of intrinsic fluorescent derivatives, incorporating azaindole moieties was achieved for the first time. Beilstein-Institut 2019-02-25 /pmc/articles/PMC6404511/ /pubmed/30873237 http://dx.doi.org/10.3762/bjoc.15.47 Text en Copyright © 2019, Wesche et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Wesche, Frank
Adihou, Hélène
Wichelhaus, Thomas A
Bode, Helge B
Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title_full Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title_fullStr Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title_full_unstemmed Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title_short Synthesis and SAR of the antistaphylococcal natural product nematophin from Xenorhabdus nematophila
title_sort synthesis and sar of the antistaphylococcal natural product nematophin from xenorhabdus nematophila
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404511/
https://www.ncbi.nlm.nih.gov/pubmed/30873237
http://dx.doi.org/10.3762/bjoc.15.47
work_keys_str_mv AT weschefrank synthesisandsaroftheantistaphylococcalnaturalproductnematophinfromxenorhabdusnematophila
AT adihouhelene synthesisandsaroftheantistaphylococcalnaturalproductnematophinfromxenorhabdusnematophila
AT wichelhausthomasa synthesisandsaroftheantistaphylococcalnaturalproductnematophinfromxenorhabdusnematophila
AT bodehelgeb synthesisandsaroftheantistaphylococcalnaturalproductnematophinfromxenorhabdusnematophila