3034696-13-1

S-HP210 Chemical Structure
3034696-13-1

Chemical Structure

S-HP210

  • CAS No.: 3034696-13-1
  • Formula:C22H19N3O2S2
  • Molecular Weight:421.54

InChIKey: AJJBGZJAGZSMJI-AWEZNQCLSA-N

SMILES: C[C@@H](C1=CC=CC=C1)NC(C2=CC=C(C=C2)CN3C(C4=C(NC3=S)C=CS4)=O)=O

Biological Activity: S-HP210 is a potent and selective glucocorticoid receptor (GR) with an IC50 value of 1.92 μM for NF-κB transrepression (TR). S-HP210 represses the LPS-induced transcription of a variety of proinflammatory genes such as IL-1β, IL-6 and COX-2. S-HP210 is nontoxic at effective doses against mouse fibroblasts 3T3 cells[1].

Cat. No. Product Name Purity Description Pricing
HY-146561
S-HP210 98.12% S-HP210 is a potent and selective glucocorticoid receptor (GR) with an IC50 value of 1.92 μM for NF-κB transrepression (TR). S-HP210 represses the LPS-induced transcription of a variety of proinflammatory genes such as IL-1β, IL-6 and COX-2. S-HP210 is nontoxic at effective doses against mouse fibroblasts 3T3 cells.
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