(S)-Mapracorat is a selective and less active glucocorticoid receptor agonist.
体外研究
(S)-Mapracorat concentration dependently inhibited TNFα secretion from activated canine PBMC with IC50 value of approximately 0.2 nM.
体内研究
Intradermal injection of compound 48/80 (50 μg in 50 μL saline) resulted in a clear wheal and flare reaction over the 60 min observation period. Topical pre-treatment with (S)-Mapracorat (0.1%) leads to significant reduction in the wheal and flare responses compared to vehicle (acetone) treated areas.
分子量
462.48
CAS号
887375-15-7
运输条件
Room temperature in continental US; may vary elsewhere.