Cyproterone acetate is a synthetic derivative of 17-hydroxyprogesterone, and acts as an androgen receptor antagonist as well as a weak progesterone receptor agonist with weak progestational and glucocorticoid activity.
More Information Supplier PagePF 3716556 is H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
More Information Supplier PagePF 3716556 is H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
More Information Supplier PagePF 3716556 is H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
More Information Supplier PagePF 3716556 is H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
More Information Supplier PagePF 3716556 is H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
More Information Supplier PageMK-5108, also known as VX-689, is a competitive inhibitor of the ATP-binding site of aurora A kinase.
More Information Supplier PageMK-5108, also known as VX-689, is a competitive inhibitor of the ATP-binding site of aurora A kinase.
More Information Supplier PageEpothilone D improves microtubule density, axonal integrity, and cognition in a transgenic mouse model of tauopathy.
More Information Supplier PageDovitinib is a small-molecule multitargeted receptor tyrosine kinase inhibitor, which inhibits Ba/F3 cells transformed to IL3 independence by ZNF198-FGFR1 or BCR-FGFR1 with IC50 values of 150 nM and 90 nM, respectively.
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