BIOMAT Database Logo BIOMAT Database Logo

Synthesis of [16,16,19(-2)H3; 19(-3)H]19-oxo-androst-4-ene-3,17-dione. 1988

V C Njar, and H R Dharmaratne, and E Caspi
Worcester Foundation for Experimental Biology, Shrewsbury, MA 01545.

The synthesis of [16,16,19(-2)H3; 19(-3)H]19-oxo-androst-4-ene-3,17-dione starting with 3 beta, 19-dihydroxyandrost-5-en-17-one is described.

UI MeSH Term Description Entries
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D000735 Androstenedione A delta-4 C19 steroid that is produced not only in the TESTIS, but also in the OVARY and the ADRENAL CORTEX. Depending on the tissue type, androstenedione can serve as a precursor to TESTOSTERONE as well as ESTRONE and ESTRADIOL. 4-Androstene-3,17-dione,delta-4-Androstenedione,4 Androstene 3,17 dione,delta 4 Androstenedione
D055598 Chemical Phenomena The composition, structure, conformation, and properties of atoms and molecules, and their reaction and interaction processes. Chemical Concepts,Chemical Processes,Physical Chemistry Concepts,Physical Chemistry Processes,Physicochemical Concepts,Physicochemical Phenomena,Physicochemical Processes,Chemical Phenomenon,Chemical Process,Physical Chemistry Phenomena,Physical Chemistry Process,Physicochemical Phenomenon,Physicochemical Process,Chemical Concept,Chemistry Process, Physical,Chemistry Processes, Physical,Concept, Chemical,Concept, Physical Chemistry,Concept, Physicochemical,Concepts, Chemical,Concepts, Physical Chemistry,Concepts, Physicochemical,Phenomena, Chemical,Phenomena, Physical Chemistry,Phenomena, Physicochemical,Phenomenon, Chemical,Phenomenon, Physicochemical,Physical Chemistry Concept,Physicochemical Concept,Process, Chemical,Process, Physical Chemistry,Process, Physicochemical,Processes, Chemical,Processes, Physical Chemistry,Processes, Physicochemical

Related Publications

V C Njar, and H R Dharmaratne, and E Caspi
Biotransformation of (+)-androst-4-ene-3,17-dione.
December 2004, Natural product research,
V C Njar, and H R Dharmaratne, and E Caspi
16-(4-Isopropylbenzylidene)androst-4-ene-3,17-dione.
February 2004, Acta crystallographica. Section C, Crystal structure communications,
V C Njar, and H R Dharmaratne, and E Caspi
Comparative placental steroid synthesis. I. Conversion of (7-3-H)-dehydroepiandrosterone to (3-H)-androst-4-ene-3,17-dione.
September 1966, Endocrinology,
V C Njar, and H R Dharmaratne, and E Caspi
11α,15α-Dihy-droxy-androst-4-ene-3,17-dione.
October 2011, Acta crystallographica. Section E, Structure reports online,
V C Njar, and H R Dharmaratne, and E Caspi
Digoxin-like immunoreactivity of 19-NOR and 19-OH-androst-4-ene-3,17-dione.
January 1986, Physiologia Bohemoslovaca,
V C Njar, and H R Dharmaratne, and E Caspi
An efficient synthesis of 5alpha-androst-1-ene-3,17-dione.
December 2006, Steroids,
V C Njar, and H R Dharmaratne, and E Caspi
Metabolites of [4-14C]androst-4-ene-3,17-dione in rabbit urine.
April 1967, The Journal of endocrinology,
V C Njar, and H R Dharmaratne, and E Caspi
Aromatization of androst-4-ene-3,17-dione by human intestinal bacteria.
October 1971, The Biochemical journal,
V C Njar, and H R Dharmaratne, and E Caspi
Microbial transformation of androst-4-ene-3,17-dione by Beauveria bassiana.
November 2006, Steroids,
V C Njar, and H R Dharmaratne, and E Caspi
Steroid total synthesis. V. ( )-estr-4-ene-3,17-dione and ( )-13 -ethylgon-4-ene-3,17-dione.
May 1972, The Journal of organic chemistry,
Copied contents to your clipboard!