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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...

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Detalles Bibliográficos
Autores principales: Tan, Qing-Wei, Ouyang, Ming-An, Gao, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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