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Total Synthesis and Stereochemical Assignment of Nostosin B
Nostosins A and B were isolated from a hydrophilic extract of Nostoc sp. strain from Iran, which exhibits excellent trypsin inhibitory activity. Nostosin A was the most potent natural tripeptide aldehyde as trypsin inhibitor up to now. Both r- and s-2-hydroxy-4-(4-hydroxy-phenyl)butanoic acid (Hhpba...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367015/ https://www.ncbi.nlm.nih.gov/pubmed/28264450 http://dx.doi.org/10.3390/md15030058 |
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author | Wang, Xiaoji Feng, Junmin Xu, Zhengshuang Ye, Tao Meng, Yi Zhang, Zhiyu |
author_facet | Wang, Xiaoji Feng, Junmin Xu, Zhengshuang Ye, Tao Meng, Yi Zhang, Zhiyu |
author_sort | Wang, Xiaoji |
collection | PubMed |
description | Nostosins A and B were isolated from a hydrophilic extract of Nostoc sp. strain from Iran, which exhibits excellent trypsin inhibitory activity. Nostosin A was the most potent natural tripeptide aldehyde as trypsin inhibitor up to now. Both r- and s-2-hydroxy-4-(4-hydroxy-phenyl)butanoic acid (Hhpba) were prepared and incorporated into the total synthesis of nostosin B, respectively. Careful comparison of the NMR spectra and optical rotation data of synthetic nostosin B (1a and 1b) with the natural product led to the unambiguous identification of the r-configuration of the Hhpba fragment, which was further confirmed by co-injection with the authentic sample on HPLC using both reversed phase column and the chiral AD-RH column. |
format | Online Article Text |
id | pubmed-5367015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-53670152017-03-31 Total Synthesis and Stereochemical Assignment of Nostosin B Wang, Xiaoji Feng, Junmin Xu, Zhengshuang Ye, Tao Meng, Yi Zhang, Zhiyu Mar Drugs Article Nostosins A and B were isolated from a hydrophilic extract of Nostoc sp. strain from Iran, which exhibits excellent trypsin inhibitory activity. Nostosin A was the most potent natural tripeptide aldehyde as trypsin inhibitor up to now. Both r- and s-2-hydroxy-4-(4-hydroxy-phenyl)butanoic acid (Hhpba) were prepared and incorporated into the total synthesis of nostosin B, respectively. Careful comparison of the NMR spectra and optical rotation data of synthetic nostosin B (1a and 1b) with the natural product led to the unambiguous identification of the r-configuration of the Hhpba fragment, which was further confirmed by co-injection with the authentic sample on HPLC using both reversed phase column and the chiral AD-RH column. MDPI 2017-02-27 /pmc/articles/PMC5367015/ /pubmed/28264450 http://dx.doi.org/10.3390/md15030058 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Xiaoji Feng, Junmin Xu, Zhengshuang Ye, Tao Meng, Yi Zhang, Zhiyu Total Synthesis and Stereochemical Assignment of Nostosin B |
title | Total Synthesis and Stereochemical Assignment of Nostosin B |
title_full | Total Synthesis and Stereochemical Assignment of Nostosin B |
title_fullStr | Total Synthesis and Stereochemical Assignment of Nostosin B |
title_full_unstemmed | Total Synthesis and Stereochemical Assignment of Nostosin B |
title_short | Total Synthesis and Stereochemical Assignment of Nostosin B |
title_sort | total synthesis and stereochemical assignment of nostosin b |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367015/ https://www.ncbi.nlm.nih.gov/pubmed/28264450 http://dx.doi.org/10.3390/md15030058 |
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