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Atomfair 9beta,11beta-Epoxy-16alpha,17,21-trihydroxypregna-1,4-diene-3,20-dione C21H26O6

Description 9beta,11beta-Epoxy-16alpha,17,21-trihydroxypregna-1,4-diene-3,20-dione (CAS No. 215095-77-5) is a high-purity synthetic steroid derivative with the molecular formula C21H26O6. This compound features a unique pentacyclic structure with epoxy, hydroxyl, and ketone functional groups, making it a valuable intermediate for pharmaceutical research and steroid chemistry. Its IUPAC name, (1S,2S,10S,11S,13R,14S,15S,17S)-13,14-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyl-18-oxapentacyclo[8.8.0.01,17.02,7.011,15]octadeca-3,6-dien-5-one , highlights its complex stereochemistry. Ideal for researchers studying glucocorticoid analogs, anti-inflammatory agents, or metabolic pathways. Available in milligram to gram quantities with ??95% purity (HPLC).

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Description

Description

9beta,11beta-Epoxy-16alpha,17,21-trihydroxypregna-1,4-diene-3,20-dione (CAS No. 215095-77-5) is a high-purity synthetic steroid derivative with the molecular formula C21H26O6. This compound features a unique pentacyclic structure with epoxy, hydroxyl, and ketone functional groups, making it a valuable intermediate for pharmaceutical research and steroid chemistry. Its IUPAC name, (1S,2S,10S,11S,13R,14S,15S,17S)-13,14-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyl-18-oxapentacyclo[8.8.0.01,17.02,7.011,15]octadeca-3,6-dien-5-one, highlights its complex stereochemistry. Ideal for researchers studying glucocorticoid analogs, anti-inflammatory agents, or metabolic pathways. Available in milligram to gram quantities with ??95% purity (HPLC).

  • CAS No: 215095-77-5
  • Molecular Formula: C21H26O6
  • Molecular Weight: 374.4
  • Exact Mass: 374.17293854
  • Monoisotopic Mass: 374.17293854
  • IUPAC Name: (1S,2S,10S,11S,13R,14S,15S,17S)-13,14-dihydroxy-14-(2-hydroxyacetyl)-2,15-dimethyl-18-oxapentacyclo[8.8.0.01,17.02,7.011,15]octadeca-3,6-dien-5-one
  • SMILES: C[C@]12C[C@H]3[C@]4(O3)[C@H]([C@@H]1C[C@H]([C@@]2(C(=O)CO)O)O)CCC5=CC(=O)C=C[C@]45C
  • Synonyms: 9,11b-Epoxidetriamcinolone, 94088-91-2, 9beta,11beta-Epoxy-16alpha,17,21-trihydroxypregna-1,4-diene-3,20-dione, UNII-U07AFW6W0O, U07AFW6W0O

Application

This epoxy-trihydroxy steroid derivative is primarily used in pharmaceutical research as a precursor for synthesizing glucocorticoid analogs with potential anti-inflammatory or immunosuppressive properties. Its unique 9??,11??-epoxy group offers a reactive site for further chemical modifications. Researchers may explore its role in modulating steroid receptor interactions or metabolic stability studies. Suitable for in vitro assays investigating steroid hormone pathways.

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