Study on the Natural Products from Two Formosan Soft Corals Lobophytum crassum and Dendronephthya griffini and the Chemical Modifications of Lobohedleolide

博士 === 國立中山大學 === 海洋生物科技暨資源學系研究所 === 95 === Marine invertebrate have been found to be a rich source of bioactive secondary metabolites. During the course of our investigation on the bioactive chemical constituents from marine invertebrates, twenty-eight metabolites have been isolated from two soft c...

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Bibliographic Details
Main Authors: Chih-Hua Chao, 趙子華
Other Authors: Jyh-Horng Sheu
Format: Others
Language:zh-TW
Published: 2007
Online Access:http://ndltd.ncl.edu.tw/handle/5unxbk
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Summary:博士 === 國立中山大學 === 海洋生物科技暨資源學系研究所 === 95 === Marine invertebrate have been found to be a rich source of bioactive secondary metabolites. During the course of our investigation on the bioactive chemical constituents from marine invertebrates, twenty-eight metabolites have been isolated from two soft coral Lobophytum crassum and Dendronephthya griffini. Investigation on L. crassum has led to the isolation of fourteen compounds, including seven new cembranoids, crassumolides A–G (1–7), and three new glycolipids (2R)-1-hydroxy -3-hexadecyloxy-propyl-β-D-arabinopyranoside (8), (2R)-1-hydroxy-3- octadecyloxy-propyl-β-D-arabinopyranoside (9), and (2R)-1-acetoxy-3- hexadecyloxy-propyl-β-D-arabino-pyranoside (10), coupled with four known compounds, lobohedleolide (11), 17-dimethylaminolobohedleolide (12), sinulariol A (13), and denticulatolide (14). Ten new steroids, griffinisterones A–J (15–24), were isolated from the soft coral D. griffini, while a known, 15-chlorogriffinsulfate (25), and three new polychlorinated acyclic compounds,griffinsulfate (26), 15-chlorogriffinol (27), and griffinol (28), were also purified from the same organism. Structures of these metabolites were identified as new natural products by extensive spectroscopic methods. Except for the use of 2D NMR, the 24-epimers of 15 and 16 were identified by a single-crystal X-ray crystallography on 15. Lobohedleolide (11), obtained in large quantity in L. crassum, has also been modified to 29–34 by chemical conversion. Oxidation with meta-chloro-peroxybenzoic acid (MCPBA) afforded compounds 29 and 30, and with selenium dioxide led to the formation of 31. Compound 34 is the product of O-coupling reaction of 11 with 1-hydroxybenzotriazole (HOBt). Over 99﹪diastereoselectivity was observed in the process of Henbest hydroxyl-directed epoxidation on 11 to yield 32. EDC-coupling with an aid of HCl salt of DMAP afforded methylester 33 in high yield, and proved the absolute stereochemistry of 3. The cytotoxicity and anti-inflammatory activities of the natural and modified compounds were also discussed herein.