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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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 |
_version_ |
1725724015797993472 |