Skip to Content
Merck

Screening of herbal constituents for aromatase inhibitory activity.

Bioorganic & medicinal chemistry (2008-09-10)
S Paoletta, G B Steventon, D Wildeboer, T M Ehrman, P J Hylands, D J Barlow
ABSTRACT

Random Forest screening of the phytochemical constituents of 240 herbs used in traditional Chinese medicine identified a number of compounds as potential inhibitors of the human aromatase enzyme (CYP19). Molecular modelling/docking studies indicated that three of these compounds (myricetin, liquiritigenin and gossypetin) would be likely to form stable complexes with the enzyme. The results of the virtual screening studies were subsequently confirmed experimentally, by in vitro (fluorimetric) assay of the compounds' inhibitory activity. The IC-50s for the flavones, myricetin and gossypetin were determined as 10 and 11 microM, respectively, whilst the flavanone, liquiritigenin, gave an IC-50 of 0.34 microM--showing about a 10-fold increase in potency, therefore, over the first generation aromatase inhibitor, aminoglutethimide.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Ketoconazole, 99.0-101.0% (EP, titration), meets EP testing specifications
Sigma-Aldrich
Daidzein, ≥98%, synthetic
Sigma-Aldrich
DL-Aminoglutethimide
Sigma-Aldrich
Myricetin, ≥96.0%, crystalline
Sigma-Aldrich
Myricetin, ≥96.0% (HPLC)
Sigma-Aldrich
Apigenin, ≥95.0% (HPLC)
Sigma-Aldrich
Genistein, from Glycine max (soybean), ~98% (HPLC)
Sigma-Aldrich
Genistein, synthetic, ≥98% (HPLC), powder