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CAS 10392-75-3

:

Pregna-1,4-diene-3,20-dione, 21-(acetyloxy)-9-chloro-11-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]-, (11β,16α)-

Description:
Pregna-1,4-diene-3,20-dione, 21-(acetyloxy)-9-chloro-11-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]-, (11β,16α)-, commonly known as a synthetic steroid, exhibits several notable characteristics. This compound is part of the corticosteroid class, which is known for its anti-inflammatory and immunosuppressive properties. Its structure features a steroid backbone with multiple functional groups, including a chloro substituent and acetoxy group, which contribute to its biological activity. The presence of hydroxyl groups enhances its solubility and reactivity, while the methylethylidene moiety may influence its pharmacokinetics and receptor binding affinity. This compound is typically utilized in medical applications, particularly in the treatment of various inflammatory conditions and disorders. Its specific stereochemistry, indicated by the (11β,16α) configuration, plays a crucial role in determining its interaction with biological targets, influencing both efficacy and safety profiles. As with many synthetic steroids, careful consideration of dosage and potential side effects is essential in clinical use.
Formula:C26H33ClO7
InChI:InChI=1S/C26H33ClO7/c1-14(28)32-13-20(31)26-21(33-22(2,3)34-26)11-18-17-7-6-15-10-16(29)8-9-23(15,4)25(17,27)19(30)12-24(18,26)5/h8-10,17-19,21,30H,6-7,11-13H2,1-5H3/t17-,18-,19-,21+,23-,24-,25-,26+/m0/s1
InChI key:InChIKey=IRHGAALQXFDXBJ-VHDCPBDGSA-N
SMILES:C(COC(C)=O)(=O)[C@]12[C@]3(C)[C@@](C[C@]1(OC(C)(C)O2)[H])([C@]4([C@](Cl)([C@@H](O)C3)[C@]5(C)C(CC4)=CC(=O)C=C5)[H])[H]
Synonyms:
  • Pregna-1,4-diene-3,20-dione, 21-(acetyloxy)-9-chloro-11-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]-, (11β,16α)-
  • 1H-Naphth[2′,1′:4,5]indeno[1,2-d][1,3]dioxole, pregna-1,4-diene-3,20-dione deriv.
  • Pregna-1,4-diene-3,20-dione, 9-chloro-11β,16α,17,21-tetrahydroxy-, cyclic 16,17-acetal with acetone, 21-acetate
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Found 4 products.