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((4-((4-hydroxy-3-(1-methylethyl)phenyl)methyl)-3
Glicoricone
enhancing the proliferation and function of immune competent cells) and plays important role in gap junction communication (e
InChiKey: IYFNEFQTYQPVOC-UHFFFAOYSA-N
which reactivates tumor suppressor genes by blocking DNA methyltransferase 1 activity and inducing its degradation
TAK-700 R-form Catalog No.:M22571-C ((4-((4-hydroxy-3-(1-methylethyl)phenyl)methyl)-3TAK 700 R form is a highly selective inhibitor of 17, 20 lyase with IC50 value of 38nM . TAK 700 is a potent and selective inhibitor of the 17, 20 lyase activity of CYP17A1 which is responsible for androgen biosynthesis. Thus, TAK 700 is selected as a candidate for treatment of prostate cancer through reducing the adrenal androgen production. As an inhibitor of CYP17A1, the selectivity of TAK 700 is important to avoid causing the drugdrug interactions
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