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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...

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Detalles Bibliográficos
Autores principales: Wang, Xiaoji, Feng, Junmin, Xu, Zhengshuang, Ye, Tao, Meng, Yi, Zhang, Zhiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
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.
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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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