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Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus

The present work constitutes a contribution to the phytochemical investigation of Cryptoporus volvatus aiming to search for effective cytotoxic constituents against tumor cell lines in vivo. Bioassay-guided separation of the ethylacetate extract of C. volvatus afforded four new isocryptoporic acid (...

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Detalles Bibliográficos
Autores principales: Zhou, Ling-Yun, Yu, Xiao-Hong, Lu, Bin, Hua, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273021/
https://www.ncbi.nlm.nih.gov/pubmed/27941653
http://dx.doi.org/10.3390/molecules21121692
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author Zhou, Ling-Yun
Yu, Xiao-Hong
Lu, Bin
Hua, Yan
author_facet Zhou, Ling-Yun
Yu, Xiao-Hong
Lu, Bin
Hua, Yan
author_sort Zhou, Ling-Yun
collection PubMed
description The present work constitutes a contribution to the phytochemical investigation of Cryptoporus volvatus aiming to search for effective cytotoxic constituents against tumor cell lines in vivo. Bioassay-guided separation of the ethylacetate extract of C. volvatus afforded four new isocryptoporic acid (ICA) derivatives, ICA-B trimethyl ester (1), ICA-E (2), ICA-E pentamethyl ester (3), and ICA-G (4), together with nine known cryptoporic acids. These isocryptoporic acids are isomers of the cryptoporic acids with drimenol instead of albicanol as the terpenoid fragment; their structures were elucidated on the basis of spectroscopic evidences (UV, IR, HRMS, and NMR) and comparison with literature values. All isolates show certain cytotoxic activities against five tumor cell lines. Among them, compound 4 showed an comparable activity to that of the positive control cis-platin, while other compounds exhibited weak cytotoxic activities.
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spelling pubmed-62730212018-12-28 Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus Zhou, Ling-Yun Yu, Xiao-Hong Lu, Bin Hua, Yan Molecules Article The present work constitutes a contribution to the phytochemical investigation of Cryptoporus volvatus aiming to search for effective cytotoxic constituents against tumor cell lines in vivo. Bioassay-guided separation of the ethylacetate extract of C. volvatus afforded four new isocryptoporic acid (ICA) derivatives, ICA-B trimethyl ester (1), ICA-E (2), ICA-E pentamethyl ester (3), and ICA-G (4), together with nine known cryptoporic acids. These isocryptoporic acids are isomers of the cryptoporic acids with drimenol instead of albicanol as the terpenoid fragment; their structures were elucidated on the basis of spectroscopic evidences (UV, IR, HRMS, and NMR) and comparison with literature values. All isolates show certain cytotoxic activities against five tumor cell lines. Among them, compound 4 showed an comparable activity to that of the positive control cis-platin, while other compounds exhibited weak cytotoxic activities. MDPI 2016-12-08 /pmc/articles/PMC6273021/ /pubmed/27941653 http://dx.doi.org/10.3390/molecules21121692 Text en © 2016 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
Zhou, Ling-Yun
Yu, Xiao-Hong
Lu, Bin
Hua, Yan
Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title_full Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title_fullStr Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title_full_unstemmed Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title_short Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus
title_sort bioassay-guided isolation of cytotoxic isocryptoporic acids from cryptoporus volvatus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273021/
https://www.ncbi.nlm.nih.gov/pubmed/27941653
http://dx.doi.org/10.3390/molecules21121692
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