Skip to search formSkip to main contentSkip to account menu

1,4-androstadiene-3,17-dione

Known as: androsta-1,4-diene-3,17-dione, boldione 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Androstadienes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
The ultimate veal calf reference experiment: hormone residue analysis data obtained by gas and liquid chromatography tandem mass spectrometry.
2007
2007
Boldenone, boldione, and milk replacers in the diet of veal calves: the effects of phytosterol content on the urinary excretion of boldenone metabolites.
Twenty-six veal calves were split into two groups and fed two milk replacers with a different content of phytosterols for 26 days… 
2002
2002
MICROBIAL TRANSFORMATION OF CHOLESTEROL BY MYCOBACTERIUM SMEGMATIS
Mycobacterium smegmatis PTCC 1307 (CIP 73.26) was used as a microbial agent to produce androsta-1,4-diene-3,17-dione (ADD) and… 
1998
1998
Enzymic aromatization of 6-alkyl-substituted androgens, potent competitive and mechanism-based inhibitors of aromatase.
To gain insight into the relationships between the aromatase inhibitory activity of 6-alkyl-substituted androgens, potent… 
1993
1993
Steroidal inhibitors as chemical probes of the active site of aromatase
1992
1992
Production of androsta-1,4-diene-3,17-dione from cholesterol using immobilized growing cells of Mycobacterium sp. NRRL B-3683 adsorbed on solid carriers
SummaryLiving cells of Mycobacterium sp. NRRL B-3683 were immobilized by adsorption on different types of solid carriers in order… 
1987
1987
Degradations of 4-cholesten-3-one and 1,4-androstadiene-3,17-dione by cholesterol-degrading bacteria.
Degradations of 4-cholesten-3-one and 1,4-androstadiene-3,17-dione, which are intermediates of microbial conversion of… 
1976
1976
Stereochemistry of a methyl-group rearrangement during the biosynthesis of lanosterol.
1. (3RS,6R)-[6-2H1,6-3H1,6-14C], (3RS,6S)-[6-2H1,6-3H1,6-14C] and (3RS)-[6-3H1,6-14C]mevalonolactones were synthesised from R… 
1975
1975
Microbial cleavage of the tomatidine spiroketal sidechain.
1968
1968
Inhibition of steroid nucleus degradation in mycobacterial transformations.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)