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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Main Authors: Qing-Wei Tan, Ming-An Ouyang, Bo Gao
Format: Article
Language:English
Published: MDPI AG 2014-04-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/19/4/4897
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spelling doaj-1c5aabbdc4044ad991cf4b472fd5bbbe2020-11-24T22:35:18ZengMDPI AGMolecules1420-30492014-04-011944897490610.3390/molecules19044897molecules19044897Three New Ring-A Modified Ursane Triterpenes from Davidia involucrataQing-Wei Tan0Ming-An Ouyang1Bo Gao2Key Laboratory of Bio-pesticide and Chemistry-Biology, Ministry of Education, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, ChinaKey Laboratory of Plant Virology of Fujian Province, Institute of Plant Virology, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, ChinaFujian International Travel Health Care Center, Fuzhou 350001, Fujian, ChinaThree 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 IC50 range from 7.26 to 47.41 μM.http://www.mdpi.com/1420-3049/19/4/4897Davidia involucrataNyssaceaetriterpenoidscytotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Qing-Wei Tan
Ming-An Ouyang
Bo Gao
spellingShingle Qing-Wei Tan
Ming-An Ouyang
Bo Gao
Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata
Molecules
Davidia involucrata
Nyssaceae
triterpenoids
cytotoxicity
author_facet Qing-Wei Tan
Ming-An Ouyang
Bo Gao
author_sort Qing-Wei Tan
title Three New Ring-A Modified Ursane Triterpenes from Davidia involucrata
title_short 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_sort three new ring-a modified ursane triterpenes from davidia involucrata
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2014-04-01
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 IC50 range from 7.26 to 47.41 μM.
topic Davidia involucrata
Nyssaceae
triterpenoids
cytotoxicity
url http://www.mdpi.com/1420-3049/19/4/4897
work_keys_str_mv AT qingweitan threenewringamodifiedursanetriterpenesfromdavidiainvolucrata
AT minganouyang threenewringamodifiedursanetriterpenesfromdavidiainvolucrata
AT bogao threenewringamodifiedursanetriterpenesfromdavidiainvolucrata
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