Description
An RORγt antagonist (IC50 = 1.1 µM in a reporter assay); inhibits RORγt-induced transcription in HEK293T cells expressing the human receptor (IC50 = 300 nM); inhibits RORγt-dependent differentiation of isolated naïve cord blood human CD4+ T cells into Th17 T helper cells
Formal name: rel-3-(1,3-benzodioxol-5-yl)-1-[(3R,5S)-3,5-dimethyl-1-piperidinyl]-3-(2-hydroxy-4,6-dimethoxyphenyl)-1-propanone
Synonyms:
Molecular weight: 441.5
CAS: 1334526-14-5
Purity: ≥98%
Formulation: A solid