Anti-oestrogenic diarylheptanoids from Aframomum melegueta with in silico oestrogen receptor alpha binding conformation similar to enterodiol and enterolactone

摘要

Aframomum melegueta is a spice widely used in African folk medicine. The chloroform soluble fraction of A. melegueta seeds yielded four new diarylheptanoids named gingerenone D (1), dihydrogingerenone A (2), dihydrogingerenone B (3), and dihydrogingerenone C (4), in addition to six known diarylheptanoids and hydroxyphenylalkanones. The most potent oestrogen receptor binding ability in an oestrogen recep-tor alpha (ERα) competitive-binding assay was for compounds 1, 2 and 5 with IC_(50) values of 50, 79 and 39 μM, respectively, compared with 18 nM for the natural steroid 17β-oestradiol (E2). In addition, the diarylheptanoids 1, 2 and 5 showed anti-oestrogenic activity in a receptor cofactor assay system for ERα, while the hydroxyphenylalkanone, [6]dehydrogingerdione, (7) exhibited an agonistic action. Results were interpreted via virtual docking of the active compounds to an ERa crystal structure, in comparison with the known oestrogenic compounds: enterodiol (END), enterolactone (ENL), genistein and E2. The anti-oestrogenic compounds 1, 2 and 5 showed a binding similarity to that of END and ENL while com-pound 7 was similar in binding to genistein and E2 interpreting its agonistic effect.