1.
J Nucl Med
; 19(3): 333-4, 1978 Mar.
Article
in English
| MEDLINE
| ID: mdl-632918
2.
J Pharm Sci
; 61(6): 888-93, 1972 Jun.
Article
in English
| MEDLINE
| ID: mdl-5046104
Subject(s)
Anti-Arrhythmia Agents/metabolism , Pyridines/metabolism , Administration, Oral , Animals , Bile/metabolism , Biotransformation , Carbon Isotopes , Chromatography, Gas , Chromatography, Thin Layer , Disopyramide/administration & dosage , Disopyramide/metabolism , Disopyramide/urine , Dogs , Feces/analysis , Female , Half-Life , Humans , Hydrolysis , Infrared Rays , Injections, Intraperitoneal , Magnetic Resonance Spectroscopy , Mass Spectrometry , Methylation , Rats , Rats, Inbred Strains , Spectrum Analysis
3.
Xenobiotica
; 2(3): 253-8, 1972 May.
Article
in English
| MEDLINE
| ID: mdl-5076571
Subject(s)
Contraceptives, Oral/metabolism , Norethynodrel/metabolism , Adult , Alkynes/urine , Carbon Isotopes , Chromatography , Estranes/urine , Ethynodiol Diacetate/urine , Feces/analysis , Female , Half-Life , Humans , Hydroxysteroids/urine , Norethynodrel/administration & dosage , Norethynodrel/urine , Stereoisomerism
4.
Xenobiotica
; 2(3): 237-52, 1972 May.
Article
in English
| MEDLINE
| ID: mdl-5076570
Subject(s)
Contraceptives, Oral/metabolism , Ethynodiol Diacetate/metabolism , Carbon Isotopes , Chromatography, Gas , Chromatography, Thin Layer , Ethynodiol Diacetate/administration & dosage , Ethynodiol Diacetate/chemical synthesis , Feces/analysis , Female , Half-Life , Humans , Hydrolysis , Infrared Rays , Isomerism , Mass Spectrometry , Mestranol/urine , Norethindrone/urine , Norethynodrel/urine , Steroids/urine , Ultraviolet Rays
5.
Appl Microbiol
; 23(1): 72-7, 1972 Jan.
Article
in English
| MEDLINE
| ID: mdl-5059623
ABSTRACT
A process is described for the microbial degradation of cholesterol and plant sterols, to produce androsta-1, 4-diene-3, 17-dione and androst-4-ene-3, 17-dione, by two newly isolated bacteria designated Mycobacterium sp. NRRL B-3683 and Mycobacterium sp. NRRL B-3805. These myocbacteria produce substantial amounts of 17-ketonic compounds without appreciable degradation of the steroid nucleus. No ring degradation inhibitory agents are necessary. The first microbiological production of 20alpha-hydroxymethylpregna-1, 4-dien-3-one is also reported.
