Description
A synthetic glucocorticoid with anti-inflammatory properties; inhibits edema by 55% in a RPA test in rabbit when administered topically (0.1% w/w); inhibits edema by 70.1% and 88.0% in croton oil-induced and PCA tests, respectively, in rat (topical, 0.1% w/w); in vivo application (0.1% w/w) to the abraded surface of cecum in rats inhibits leukocyte adhesion (43.3% incidence versus 100% for controls) and lowers the total number of intraperitoneal leukocytes from 270 million to 121 million 3 days post surgery; acts as an agonist at the Smo receptor (EC50 = 1,100 nM)
Formal name: 21-chloro-9-fluoro-11β-hydroxy-16α,17-[(1-methylethylidene)bis(oxy)]-pregn-4-ene-3,20-dione
Synonyms: SQ 18,566
Molecular weight: 455
CAS: 3093-35-4
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Endocrinology & Metabolism|Hormones & Receptors|Glucocorticoids & Mineralocorticoids||Research Area|Immunology & Inflammation|Allergy||Research Area|Immunology & Inflammation|Gastric Disease||Research Area|Immunology & Inflammation|Innate Immunity