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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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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 |
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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 |
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