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Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor

A new centrosymmetric cyclohexapeptide, aspersymmetide A (1), together with a known peptide, asperphenamate (2), was isolated from the fungus Aspergillus versicolor isolated from a gorgonian coral Carijoa sp., collected from the South China Sea. The chemical structure of 1 was elucidated by analyzin...

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Autores principales: Hou, Xue-Mei, Zhang, Ya-Hui, Hai, Yang, Zheng, Ji-Yong, Gu, Yu-Cheng, Wang, Chang-Yun, Shao, Chang-Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706052/
https://www.ncbi.nlm.nih.gov/pubmed/29165326
http://dx.doi.org/10.3390/md15110363
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author Hou, Xue-Mei
Zhang, Ya-Hui
Hai, Yang
Zheng, Ji-Yong
Gu, Yu-Cheng
Wang, Chang-Yun
Shao, Chang-Lun
author_facet Hou, Xue-Mei
Zhang, Ya-Hui
Hai, Yang
Zheng, Ji-Yong
Gu, Yu-Cheng
Wang, Chang-Yun
Shao, Chang-Lun
author_sort Hou, Xue-Mei
collection PubMed
description A new centrosymmetric cyclohexapeptide, aspersymmetide A (1), together with a known peptide, asperphenamate (2), was isolated from the fungus Aspergillus versicolor isolated from a gorgonian coral Carijoa sp., collected from the South China Sea. The chemical structure of 1 was elucidated by analyzing its NMR spectroscopy and MS spectrometry data, and the absolute configurations of the amino acids of 1 were determined by Marfey’s method and UPLC-MS analysis of the hydrolysate. Aspersymmetide A (1) represents the first example of marine-derived centrosymmetric cyclohexapeptide. Moreover, 1 exhibited weak cytotoxicity against NCI-H292 and A431 cell lines at the concentration of 10 μM.
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spelling pubmed-57060522017-12-04 Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor Hou, Xue-Mei Zhang, Ya-Hui Hai, Yang Zheng, Ji-Yong Gu, Yu-Cheng Wang, Chang-Yun Shao, Chang-Lun Mar Drugs Short Note A new centrosymmetric cyclohexapeptide, aspersymmetide A (1), together with a known peptide, asperphenamate (2), was isolated from the fungus Aspergillus versicolor isolated from a gorgonian coral Carijoa sp., collected from the South China Sea. The chemical structure of 1 was elucidated by analyzing its NMR spectroscopy and MS spectrometry data, and the absolute configurations of the amino acids of 1 were determined by Marfey’s method and UPLC-MS analysis of the hydrolysate. Aspersymmetide A (1) represents the first example of marine-derived centrosymmetric cyclohexapeptide. Moreover, 1 exhibited weak cytotoxicity against NCI-H292 and A431 cell lines at the concentration of 10 μM. MDPI 2017-11-22 /pmc/articles/PMC5706052/ /pubmed/29165326 http://dx.doi.org/10.3390/md15110363 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 Short Note
Hou, Xue-Mei
Zhang, Ya-Hui
Hai, Yang
Zheng, Ji-Yong
Gu, Yu-Cheng
Wang, Chang-Yun
Shao, Chang-Lun
Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title_full Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title_fullStr Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title_full_unstemmed Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title_short Aspersymmetide A, a New Centrosymmetric Cyclohexapeptide from the Marine-Derived Fungus Aspergillus versicolor
title_sort aspersymmetide a, a new centrosymmetric cyclohexapeptide from the marine-derived fungus aspergillus versicolor
topic Short Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706052/
https://www.ncbi.nlm.nih.gov/pubmed/29165326
http://dx.doi.org/10.3390/md15110363
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