【摘 要】
：
Six eremophilane sesquiterpenes were obtained from a marine fungus Penicillium sp. BL27-2. Their structures were elucidatedas 3-acetyl-9, 7 (11)-dien-7ot-hydrox
【机 构】
：
Department of Plant Pathology,School of Traditional Chinese Materia Medica,College of Chemical Engin
【基金项目】
：
国家高技术研究发展计划(863计划);国家重点基础研究发展计划(973计划)
论文部分内容阅读
Six eremophilane sesquiterpenes were obtained from a marine fungus Penicillium sp. BL27-2. Their structures were elucidatedas 3-acetyl-9, 7 (11)-dien-7ot-hydroxy-8-oxoeremophilane (1), 3-acetyl-13-deoxyphomenone (2), Sporogen-AO 1 (3), 7-hydro-xypetasol (4), 8α-hydroxy-13-deo -xyphomenone (5) and 6-dehydropetasol (6) based on detailed NMR analysis. 1 was a newcompound and 2 was obtained as a new natural compound. These compounds were assayed for their cytotoxic activity on P388,A549, HL60, BEL7402 and K562 cell lines by the MTT method. The assay results suggested the epoxide tings in eremophilanemolecules were essential for their activity, and acetylation could enhance their activity.2008 Yong Fu Huang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
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