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Inhibition of Monoamine Oxidase by Stilbenes from Rheum palmatum.


ABSTRACT: Seven stilbenes and one catechin were bioactivity-guidedly isolated from the rhizomes of Rheum palmatem. Their structures were identified as piceatannol (1), resveratrol (2), piceid (3), rhapontigenin (4), piceatannol-3´-O-?-D-glucopyranoside (5), rhaponticin (6), catechin (7) and desoxyrhapontigenin (8). Anti-monoamine oxidase (MAO) activities of compounds 1-8 were tested. Compounds 1 and 8 showed significant MAO inhibitory activities with IC50 values 16.4 ± 1.5 ?M and 11.5 ± 1.1, respectively, when the IC50 value of iproniazid as a standard was 6.5 ± 0.5 ?M. The selectivity of compounds 1-8 against MAO-A and MAO-B were also evaluated. The results showed that compounds 4?6?8 preferred to inhibit MAO-A rather than MAO-B with selectivity values ([IC50 of MAO-B]/ [IC50 of MAO-A]) of 4.74, 10.01 and 9.42, respectively. The preliminary structure-activity relationships (SARs) of these compounds were discussed and the molecular modeling was also performed to explore the binding mode of inhibitors at the active site of MAO-A and MAO-B.

SUBMITTER: Wei B 

PROVIDER: S-EPMC5316268 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

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Inhibition of Monoamine Oxidase by Stilbenes from Rheum palmatum.

Wei Bo B   Yang Zhong-Duo ZD   Shi Dan-Feng DF   Yao Xiao-Jun XJ   Wang Ming-Gang MG  

Iranian journal of pharmaceutical research : IJPR 20160101 4


Seven stilbenes and one catechin were bioactivity-guidedly isolated from the rhizomes of <i>Rheum palmatem</i>. Their structures were identified as piceatannol (1), resveratrol (2), piceid (3), rhapontigenin (4), piceatannol-3<i>´</i>-O-β-D-glucopyranoside (5), rhaponticin (6), catechin (7) and desoxyrhapontigenin (8). Anti-monoamine oxidase (MAO) activities of compounds 1-8 were tested. Compounds 1 and 8 showed significant MAO inhibitory activities with IC<sub>50</sub> values 16.4 ± 1.5 μM and  ...[more]

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