
CAS 52647-07-1: (9xi,11beta,16beta,17E)-9-fluoro-11,20-dihydroxy-16-methyl-3-oxopregna-1,4,17-trien-21-al
Formula:C22H27FO4
InChI:InChI=1/C22H27FO4/c1-12-8-16-15-5-4-13-9-14(25)6-7-21(13,3)22(15,23)18(27)10-20(16,2)19(12)17(26)11-24/h6-7,9,11-12,15-16,18,26-27H,4-5,8,10H2,1-3H3/b19-17+/t12-,15-,16-,18-,20-,21-,22?/m0/s1
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Betamethasone Enol Aldehyde E Isomer
CAS:Formula:C22H27FO4Color and Shape:White To Off-White SolidMolecular weight:374.45(E)-Betamethasone-∆17,20 21-Aldehyde
CAS:Formula:C22H27FO4Color and Shape:NeatMolecular weight:374.45Betamethasone enol aldehyde E isomer
CAS:Controlled ProductBetamethasone enol aldehyde E isomer is a synthetic corticosteroid compound, which is a derivative of betamethasone. It is sourced through chemical synthesis methods that modify the steroid structure to expose particular isomeric forms, enhancing its specificity for receptor binding. Its mode of action primarily involves binding to glucocorticoid receptors, inhibiting the transcription of certain pro-inflammatory cytokines, and thereby reducing inflammation and altering immune responses. Betamethasone enol aldehyde E isomer is utilized extensively in research settings to study the effects of corticosteroids on cellular pathways, including those involved in immune modulation and inflammatory processes. Its applications extend to investigations on its efficacy in treating allergic reactions, autoimmune disorders, and various dermatological conditions. Moreover, this compound serves as a valuable tool for elucidating the mechanisms of steroid hormone action at the molecular level, contributing to the development of novel therapeutic strategies.Formula:C22H27FO4Purity:Min. 95 Area-%Color and Shape:White PowderMolecular weight:374.45 g/mol