600-81-7

Basic information

• Product Name: 4-Pregnen-7beta-ol-3,20-dione
• Synonyms: Pregn-4-ene-3,20-dione, 7-hydroxy-, (7β)-
• CAS NO: 600-81-7
• Molecular Formula: C₂₁H₃₀O₃
• Molecular Weight: 330.46
• Mol File: 600-81-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 188-191 °C
• Boiling Point: 489.1±45.0 °C(Predicted)
• Appearance: /
• Density: 1.15±0.1 g/cm3(Predicted)
• PKA: 14.38±0.70(Predicted)
• CAS DataBase Reference: 4-Pregnen-7beta-ol-3,20-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pregnen-7beta-ol-3,20-dione(600-81-7)
• EPA Substance Registry System: 4-Pregnen-7beta-ol-3,20-dione(600-81-7)

Safety Data

• Hazardous Substances Data: 600-81-7(Hazardous Substances Data)

Upstream product

• 57-83-0 Progesterone 
• 1312467-35-8 3,20-bis(ethylenedioxy)pregn-5-en-7β-ol 
• 71379-22-1 3,20-bis(ethylenedioxy)pregn-5-en-7-one 
• 57-83-0 progesterone 

Downstream Products

• 1162-56-7 6-dehydroprogesterone 

Relevant articles and documents

Novel metabolites of dehydroepiandrosterone and progesterone obtained in Didymosphearia igniaria KCH 6670 culture

Dehydroepiandrosterone (DHEA) (10) and its five derivatives: testosterone (1), androstenedione (2), 17α-methyltestosterone (6), progesterone (13) and pregnenolone (14) were subjected to microbial transformation by the filamentous fungus Didymosphaeria igniaria KCH 6670. The predominant metabolism of the incubated 5-ene steroids (10 and 14) occurred through 3β-hydroxy-steroid dehydrogenase/5,4-en isomerase pathways resulting in the generation of a 4-en-3-oxo system on ring-A. The transformations of C 19 steroids (1, 2, and 10) included a hydroxylation at 7α position, ketone-alcohol interconversion at C-17 and reduction of the double bond at C-4 and 3-keto group to the 3β-alcohol with 5α- stereochemistry at A/B ring. D. igniaria also carried out 6(7)-dehydrogenation and 6,7β-epoxidation during transformation of DHEA. Under these conditions transformation of DHEA (10) gave four products: 7α-hydroxyandrost-4-en-3, 17-dione (4), 17β-hydroxyandrost-4,6-dien-3-one (11), 17β- hydroxyandrost-6β-epoxy-4-en-3-one (12) and 3β,17β-dihydroxy- 5α-androstane (5). The compounds 11 and 12 are identified as DHEA metabolites for the first time. The transformation of C21 steroids (13 and 14) led to the mixture of mono- (mainly 11α- and 15β-) and dihydroxy- (7α,15β-; 14α,15β-; 11α,15β-; 11α,14α-) products. 7α,15β-Dihydroxypregnan-4-en-3,20- dione (18) and 14α,15β-dihydroxypregnan-4-en-3,20-dione (19) were found to be new compounds. The main product of transformation of 17α-methyltestosterone (6) was 12β-hydroxy-17α- methyltestosterone (7). The results of these transformations demonstrate the dependence of hydroxylation position on the structure of steroid nucleus.

Studies on the metabolism of C21 steroids in rat liver. Hydroxylation of progesterone in rat liver microsomes.

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