(S)-Mapracorat

  Cat. No.:  DC20017  
Chemical Structure
887375-15-7
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More than 5000 active chemicals with high quality for research!
Field of application
(S)-Mapracorat is a selective and less active glucocorticoid receptor agonist.
Cas No.: 887375-15-7
Synonyms: (Synonyms: (S)-ZK-245186; (S)-BOL-303242X)
SMILES: CC1=NC2=C(C=C1)C(=CC=C2)NC[C@@](CC(C)(C)C3=CC(=CC4=C3OCC4)F)(C(F)(F)F)O
Formula: C25H26F4N2O2
M.Wt: 462.48
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: In Vitro (S)-Mapracorat concentration dependently inhibited TNFα secretion from activated canine PBMC with IC50 value of approximately 0.2 nM. In Vivo 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%) and triamcinolone acetonide (0.015%) led to significant reduction in the wheal and flare responses compared to vehicle (acetone) treated areas. However, once daily topical administration of triamcinolone acetonide significantly reduced skin fold thickness from day 8 to 14, whereas no such reduction was observed for (S)-Mapracorat.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
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