Novel Sesquiterpenoid from Pachira aquatica

CNU IR > Pharmacy and Science > 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium > Item 310902800/24249

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/24249

Title:	Novel Sesquiterpenoid from Pachira aquatica
Authors:	Lin-Yang Cheng (鄭霖陽) Chin-Yen Chen (陳晉彦) Chang-Hui Liao (廖長輝) Mei-Ing Chung (鍾美英) Jih-Jung Chen (陳日榮)
Date:	2011
Issue Date:	2011-06-23 14:57:34 (UTC+8)
Abstract:	Pachira aquatica Aublet (Bombacaceae) is an evergreen tree, distributed throughout tropical America, being widely cultivated in Asiatic countries, introduced tomainly in China, Japan and Taiwan. Cadinane type sesquiterpenoids, sesquiterpene lactones, and triterpenes are widely distributed in plants of the family Bombacaceae. Many of these compounds exhibit antiangiogenic, hypotensive, and antimicrobial activities. Investigation of rc-hexane-soluble fraction of the stem of R aquatica has led to the isolation of a new cadinane type sesquiterpene, pachiraquiatin A (1), together with ten known compounds, including seven flavonoids, 5-hydroxyaurnetin (2), kaempferol 3,7,4'-trimethyl ether (3), santin 7-methyl ether 3,5,6,7,8,3', 4'-heptamethoxyflavone (5), calycopterin (6), retusin (7), and -dihydroxy-3,7-dimethoxyflavone (8), two cadalene type sesquiter- penes, isohemigossylic acid lactone 7-methyl ether (9) and hibiscolactone A (10), and a triterpenoid, lupenone (11). The structures of the above isolates were determined through spectroscopic and MS analyses. This symposium describes the structural elucidation of 1 and the biological activities of the isolates.
Relation:	2011年台俄有機、藥物與生物化學交流暨藥物化學研討會，起迄日：2011/04/06~2011/04/05，地點：溪頭台大實驗林
Appears in Collections:	[Pharmacy and Science] 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium

Files in This Item:

File	Description	Size	Format
pp-33.pdf		82Kb	Adobe PDF	552	View/Open

Loading...