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16α,17α-Epoxyprogesterone|CS-0145392|1097-51-4

16α,17α-Epoxyprogesterone

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Sku TS246CS-0145392_100_G
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Product Information

Product Name
16α,17α-Epoxyprogesterone
Brand Name
ChemScene
Product Number
CS-0145392
CAS
1097-51-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
101966
IUPAC Name
(1R,2S,4R,6S,7S,10S,11R)-6-acetyl-7,11-dimethyl-5-oxapentacyclo8.8.0.02,7.04,6.011,16octadec-15-en-14-one
InChI Key
LHNVKVKZPHUYQO-SRWWVFQWSA-N
SMILES
CC(=O)C@12C@H(O1)CC@@H3C@@2(CCC@H4C@H3CCC5=CC(=O)CCC@45C)C

References Data Source From Pubchem

Highly efficient conversion of androstenedione into dehydroepiandrosterone through the construction of molecular machines
Publication Name: Systems Microbiology and Biomanufacturing
Publication Date: 2025-07-01
DOI: 10.1007/s43393-025-00381-0

Removal efficiencies of natural and synthetic progesterones in hospital wastewater treated by different disinfection processes
Publication Name: Frontiers of Environmental Science & Engineering
Publication Date: 2022-03-04
DOI: 10.1007/s11783-022-1558-z

Different genome-wide transcriptome responses of Nocardioides simplex VKM Ac-2033D to phytosterol and cortisone 21-acetate
Publication Name: BMC Biotechnology
Publication Date: 2021-01-13
DOI: 10.1186/s12896-021-00668-9

Metabolic fate of pregnene-based steroids in the lactonization pathway of multifunctional strain Penicillium lanosocoeruleum
Publication Name: Microbial Cell Factories
Publication Date: 2018-06-26
DOI: 10.1186/s12934-018-0948-1

Heterologous expression and characterization of a 3-ketosteroid-∆1-dehydrogenase from Gordonia neofelifaecis and its utilization in the bioconversion of androst-4,9(11)-dien-3,17-dione
Publication Name: 3 Biotech
Publication Date: 2017-04-08
DOI: 10.1007/s13205-017-0601-4