CAS 123013-22-9
:(11β,16β)-9-Fluoro-11-hydroxy-21-methoxy-16-methyl-17-(1-oxopropoxy)pregna-1,4-diene-3,20-dione
Description:
The chemical substance known as "(11β,16β)-9-Fluoro-11-hydroxy-21-methoxy-16-methyl-17-(1-oxopropoxy)pregna-1,4-diene-3,20-dione," with the CAS number 123013-22-9, is a synthetic glucocorticoid. This compound features a steroid backbone, characterized by its four fused carbon rings, which is typical of steroid hormones. The presence of a fluorine atom at the 9-position enhances its anti-inflammatory potency, while the hydroxyl group at the 11-position contributes to its glucocorticoid activity. The methoxy group at the 21-position and the propoxy carbonyl at the 17-position further modify its pharmacological properties, potentially influencing its solubility and receptor binding affinity. This compound is primarily studied for its therapeutic applications in treating inflammatory and autoimmune conditions due to its ability to modulate immune responses. As with many glucocorticoids, it may exhibit a range of biological effects, including anti-inflammatory, immunosuppressive, and metabolic actions, making it a subject of interest in both clinical and pharmaceutical research.
Formula:C26H35FO6
InChI:InChI=1/C26H35FO6/c1-6-22(31)33-26(21(30)14-32-5)15(2)11-19-18-8-7-16-12-17(28)9-10-23(16,3)25(18,27)20(29)13-24(19,26)4/h9-10,12,15,18-20,29H,6-8,11,13-14H2,1-5H3/t15-,18-,19-,20-,23-,24-,25-,26-/m0/s1
InChI key:InChIKey=ZMYGOSBRLPSJNB-SOMXGXJRSA-N
SMILES:C(COC)(=O)[C@]1(OC(CC)=O)[C@]2(C)[C@@](C[C@@H]1C)([C@]3([C@](F)([C@@H](O)C2)[C@]4(C)C(CC3)=CC(=O)C=C4)[H])[H]
Synonyms:- (+)-9-Fluoro-11beta,17-dihydroxy-21-methoxy-16beta-methylpregna-1,4-diene-3,20-dione 17-propionate
- (11Beta,16Beta)-9-Fluoro-11-Hydroxy-21-Methoxy-16-Methyl-3,20-Dioxopregna-1,4-Dien-17-Yl Propanoate
- (11β,16β)-9-Fluoro-11-hydroxy-21-methoxy-16-methyl-17-(1-oxopropoxy)pregna-1,4-diene-3,20-dione
- (9Xi,11Beta,16Beta)-9-Fluoro-11-Hydroxy-21-Methoxy-16-Methyl-3,20-Dioxopregna-1,4-Dien-17-Yl Propanoate
- 21-O-Methyl-17-O-propionylbetamethasone
- Amelometasone [INN]
- Betamethasone 17-propionate 21-methoxide
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11-hydroxy-21-methoxy-16-methyl- 17-(1-oxopropoxy)-, (11-beta,16-beta)-
- Pregna-1,4-diene-3,20-dione, 9-fluoro-11-hydroxy-21-methoxy-16-methyl-17-(1-oxopropoxy)-, (11β,16β)-
- Ts-410
- Unii-T01B0Rce7T
- Amelometasone
- [(8S,10S,11S,13S,14S,16S,17R)-9-fluoro-11-hydroxy-17-(2-methoxyacetyl)-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
Amelometasone
CAS:Amelometasone is a biochemical.Formula:C26H35FO6Color and Shape:SolidMolecular weight:462.55[(8S,9R,10S,11S,13S,14S,16S,17R)-9-Fluoro-11-Hydroxy-17-(2-Methoxyacetyl)-10,13,16-Trimethyl-3-Oxo-6,7,8,11,12,14,15,16-Octahydrocyc lopenta[a]Phenanthren-17-Yl] Propanoate
CAS:Controlled Product<p>Betamethasone is a corticosteroid that is used to treat inflammation, ankylosing spondylitis, and rheumatoid arthritis. It has been shown to have efficacy in the treatment of pediatric patients with asthma, as well as animal models of cardiac arrest and stroke. Betamethasone has also been shown to be effective in the treatment of potassium ion-associated death due to cardiac arrhythmia or repolarization abnormalities. This drug can be administered orally or topically; it binds to the glucocorticoid receptor on cells and modulates gene transcription. The primary mechanism of action for betamethasone is not fully understood but may involve inhibition of protein synthesis and suppression of inflammatory cells.</p>Formula:C26H35FO6Purity:Min. 95%Molecular weight:462.55 g/mol

