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Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata
Three new ursane triterpenes, 3α,19α-dihydroxy-2-nor-urs-12-en-23,28-dioic acid-23-methyl ester (1), 19α,23-dihydroxy-3-oxo-2-nor-urs-12-en-28-oic acid (2), and 2,3-seco-3-methoxy-3,19α,23-trihydroxy-urs-12-en-2-al-28-oic acid (3), were isolated from the MeOH extract of the branch barks of Davidia i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271727/ https://www.ncbi.nlm.nih.gov/pubmed/24747647 http://dx.doi.org/10.3390/molecules19044897 |
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author | Tan, Qing-Wei Ouyang, Ming-An Gao, Bo |
author_facet | Tan, Qing-Wei Ouyang, Ming-An Gao, Bo |
author_sort | Tan, Qing-Wei |
collection | PubMed |
description | Three new ursane triterpenes, 3α,19α-dihydroxy-2-nor-urs-12-en-23,28-dioic acid-23-methyl ester (1), 19α,23-dihydroxy-3-oxo-2-nor-urs-12-en-28-oic acid (2), and 2,3-seco-3-methoxy-3,19α,23-trihydroxy-urs-12-en-2-al-28-oic acid (3), were isolated from the MeOH extract of the branch barks of Davidia involucrata, together with six known compounds. Their structures were elucidated by means of various spectroscopic analyses. The isolated triterpenes provide important evolutionary and chemotaxonomic knowledge about the monotypic genus Davidia. Five of the identified compounds showed moderate cytotoxicities against the cell proliferation of SGC-7901, MCF-7, and BEL-7404 with IC(50) range from 7.26 to 47.41 μM. |
format | Online Article Text |
id | pubmed-6271727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62717272019-01-02 Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata Tan, Qing-Wei Ouyang, Ming-An Gao, Bo Molecules Article Three new ursane triterpenes, 3α,19α-dihydroxy-2-nor-urs-12-en-23,28-dioic acid-23-methyl ester (1), 19α,23-dihydroxy-3-oxo-2-nor-urs-12-en-28-oic acid (2), and 2,3-seco-3-methoxy-3,19α,23-trihydroxy-urs-12-en-2-al-28-oic acid (3), were isolated from the MeOH extract of the branch barks of Davidia involucrata, together with six known compounds. Their structures were elucidated by means of various spectroscopic analyses. The isolated triterpenes provide important evolutionary and chemotaxonomic knowledge about the monotypic genus Davidia. Five of the identified compounds showed moderate cytotoxicities against the cell proliferation of SGC-7901, MCF-7, and BEL-7404 with IC(50) range from 7.26 to 47.41 μM. MDPI 2014-04-17 /pmc/articles/PMC6271727/ /pubmed/24747647 http://dx.doi.org/10.3390/molecules19044897 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Tan, Qing-Wei Ouyang, Ming-An Gao, Bo Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title | Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title_full | Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title_fullStr | Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title_full_unstemmed | Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title_short | Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata |
title_sort | three new ring-a modified ursane triterpenes from davidia involucrata |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271727/ https://www.ncbi.nlm.nih.gov/pubmed/24747647 http://dx.doi.org/10.3390/molecules19044897 |
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