Cayman Chemical, 293753-05-6

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  • Cayman Chemical

    A selective inverse agonist of RORα, competitively inhibiting the binding of 25-hydroxycholesterol to the ligand binding domain (Ki = 220 nM) and inhibiting constitutive transactivation activity (IC50 = 480 nM); evokes RORα-dependent effects both in vitro and in vivo.