Potent inhibitors of equine steroid isomerase EcaGST A3-3

التفاصيل البيبلوغرافية
العنوان: Potent inhibitors of equine steroid isomerase EcaGST A3-3
المؤلفون: Lindström, Helena, Mazari, Aslam M. A., Musdal, Yaman, Mannervik, Bengt
المصدر: PLOS ONE. 14(3)
مصطلحات موضوعية: neurokemi med molekylär neurobiologi, Neurochemistry with Molecular Neurobiology
الوصف: Equine glutathione transferase A3-3 (EcaGST A3-3) belongs to the superfamily of detoxication enzymes found in all higher organisms. However, it is also the most efficient steroid double-bond isomerase known in mammals. Equus ferus caballus shares the steroidogenic pathway with Homo sapiens, which makes the horse a suitable animal model for investigations of human steroidogenesis. Inhibition of the enzyme has potential for treatment of steroid-hormone-dependent disorders. Screening of a library of FDA-approved drugs identified 16 out of 1040 compounds, which at 10 mu M concentration afforded at least 50% inhibition of EcaGST A3-3. The most potent inhibitors, anthralin, sennoside A, tannic acid, and ethacrynic acid, were characterized by IC50 values in the submicromolar range when assayed with the natural substrate Delta(5)-androstene-3,17-dione.
وصف الملف: print
الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-168366Test
https://doi.org/10.1371/journal.pone.0214160Test
قاعدة البيانات: SwePub
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0214160