Abstract
The biotransformation of dehydroepiandrosterone (1) with Macrophomina phaseolina was investigated. A total of eight metabolites were obtained which were characterized as androstane-3,17-dione (2), androst-4-ene-3,17-dione (3), androst-4-ene-17β-ol-3-one (4), androst-4,6-diene-17β-ol-3-one (5), androst-5-ene-3β,17β-diol (6), androst-4-ene-3β-ol-6,17-dione (7), androst-4-ene-3β,7β,17β-triol (8), and androst-5-ene- 3β,7α,17β-triol (9). All the transformed products were screened for enzyme inhibition, among which four were found to inhibit the β-glucuronidase enzyme, while none inhibited the α-chymotrypsin enzyme. © 2012 Informa UK, Ltd.
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Choudhary, M. I., Zafar, S., Khan, N. T., Ahmad, S., Noreen, S., Marasini, B. P., … Atta-Ur-Rahman. (2012). Biotransformation of dehydroepiandrosterone with Macrophomina phaseolina and β-glucuronidase inhibitory activity of transformed products. Journal of Enzyme Inhibition and Medicinal Chemistry, 27(3), 348–355. https://doi.org/10.3109/14756366.2011.590804
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