| Literature DB >> 26784520 |
Ge Liao1, Wen-Li Mei2, Wen-Hua Dong2, Wei Li2, Pei Wang2, Fan-Dong Kong2, Cui-Juan Gai2, Xi-Qiang Song3, Hao-Fu Dai4.
Abstract
Seven new 2-(2-phenylethyl)chromone derivatives (1-7) including a chlorinated one (4), together with eight known ones (8-15), were isolated from the EtOAc extract of artificial agarwood originating from Aquilaria sinensis (Lour.) Gilg. All structures including the absolute configurations were unambiguously elucidated by spectroscopic (NMR, UV, IR, MS) methods, Mosher's method, and comparison with reported data in the literatures. Among those, compounds 8, 12, and 14 exhibited significant inhibition against α-glucosidase in vitro with IC50 values of 0.15, 0.05, and 0.09 mM, respectively (with acarbose as the positive control; IC50: 0.98 mM). In addition, compounds 3, 9, 11, and 14 showed weak inhibitory activity against AChE; and compounds 12 and 13 displayed weak cytotoxicity against human gastric cell line (SGC-7901) among three types of tested human cancer cell lines (BEL-7402, K562, and SGC-7901).Entities:
Keywords: 2-(2-Phenylethyl)chromone; Agarwood; Aquilaria sinensis; Biological activity
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Year: 2016 PMID: 26784520 DOI: 10.1016/j.fitote.2016.01.011
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882