PPARgamma agonist from Chromolaena odorata.

Article Details

Citation

Zhang ML, Irwin D, Li XN, Sauriol F, Shi XW, Wang YF, Huo CH, Li LG, Gu YC, Shi QW

PPARgamma agonist from Chromolaena odorata.

J Nat Prod. 2012 Dec 28;75(12):2076-81. doi: 10.1021/np300386d. Epub 2012 Nov 27.

PubMed ID
23186307 [ View in PubMed
]
Abstract

A phytochemical investigation of Chromolaena odorata resulted in the isolation of five new compounds, 5aalpha,6,9,9abeta,10-pentahydro-10beta-hydroxy-7-methylanthra[1,2-d][1,3]dioxol- 5-one (1), 1,2-methylenedioxy-6-methylanthraquinone (2), 3-hydroxy-1,2,4-trimethoxy-6-methylanthraquinone (3), 3-hydroxy-1,2-dimethoxy-6-methylanthraquinone (4), and 7-methoxy-7-epi-medioresinol (5), together with 12 known compounds, odoratin (6), 3beta-acetyloleanolic acid (7), ursolic acid (8), ombuin (9), 4,2'-dihydroxy-4',5',6'-trimethoxychalcone (10), (-)-pinoresinol (11), austrocortinin (12), tianshic acid (13), cleomiscosin D (14), (-)-medioresinol (15), (-)-syringaresinol (16), and cleomiscosin A (17). All the compounds were evaluated for their PPARgamma transactivation activity, and compound 6 showed moderate activity with an EC(50) value of 3.10 muM.

DrugBank Data that Cites this Article

Binding Properties
DrugTargetPropertyMeasurementpHTemperature (°C)
RosiglitazonePeroxisome proliferator-activated receptor gammaEC 50 (nM)900N/AN/ADetails