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2-(2-phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing.

Fitoterapia (2014-07-30)
Wei Li, Cai-Hong Cai, Wen-Hua Dong, Zhi-Kai Guo, Hao Wang, Wen-Li Mei, Hao-Fu Dai
RÉSUMÉ

Three new 2-(2-phenylethyl)chromone derivatives (1-3), together with thirteen known ones (4-16), were isolated from the EtOAc extract of Chinese agarwood induced by artificial holing, originating from Aquilaria sinensis (Lour.) Gilg (Thymelaeaceae). The chemical structures of the new compounds were identified by spectroscopic techniques (UV, IR, MS, 1D and 2D NMR). Compounds 1, 6, 15 and 16 exhibited inhibitory effects on Staphylococcus aureus, and compounds 15 and 16 showed inhibitory effects on Ralstonia solanacearum. Compounds 1-3, 7, 9, 11, 12, 15 and 16 exhibited acetylcholinesterase inhibitory activity. A possible biogenetic pathway of compounds 1-16 was proposed to show the relationships between diepoxy-tetrahydro-2-(2-phenylethyl)chromones, epoxy-tetrahydro-2-(2-phenylethyl) chromones, tetrahydro-2-(2-phenylethyl)chromones, and 2-(2-phenylethyl)chromones of the flidersia type, the four main types of 2-(2-phenylethyl)chromones found in agarwood, on the basis of their appearances in different stage of agarwood formation.

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Sigma-Aldrich
Acide 5,5′-Dithiobis(2-nitrobenzoïque), ≥98%, BioReagent, suitable for determination of sulfhydryl groups
Sigma-Aldrich
Acide 5,5′-Dithiobis(2-nitrobenzoïque), ReagentPlus®, 99%
Sigma-Aldrich
Acetylthiocholine iodide, ≥98% (TLC), powder or crystals
Sigma-Aldrich
Acetylthiocholine iodide, ≥99.0% (AT)