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Ent-abietanes from the Godavari mangrove, Ceriops decandra: Absolute configuration and NF-κB inhibitory activity
Zhong-Ping Jiang1, Li-Wen Tian2, Li Shen1
1Marine Drugs Research Center, College of Pharmacy, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, PR China.
Abstract:
Nine new ent-abietanes, named decandrols A-I (1-9), which could be categorized into three groups (1, 2-6, 7-9), were isolated from the roots of an Indian mangrove, Ceriops decandra, collected in the swamp of Godavari estuary, Andhra Pradesh, together with six previously reported abietanes (10-15), of which the absolute configurations were first determined. The relative and absolute configurations of these compounds were unambiguously established by HR-ESIMS, extensive 1D and 2D NMR investigations, single-crystal X-ray diffraction analysis with Cu Kα radiation, and quantum-chemical electronic circular dichroism (ECD) calculations. Decandrol A (1) is a rare C9-spirofused 7,8-seco-ent-abietane, whereas 2-15 are typically tricyclic ent-abietanes. Decandrols C (3) and E (5) exhibited significant NF-κB inhibitory activity at the concentration of 100 μM.
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