BIOMAT Database Logo BIOMAT Database Logo

[Metabolism and determination of 3beta-hydroxy-17-keto-androstene (epiandrosterone) in humans]. 1956

M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY

UI MeSH Term Description Entries
D001826 Body Fluids Liquid components of living organisms. Body Fluid,Fluid, Body,Fluids, Body
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000728 Androgens Compounds that interact with ANDROGEN RECEPTORS in target tissues to bring about the effects similar to those of TESTOSTERONE. Depending on the target tissues, androgenic effects can be on SEX DIFFERENTIATION; male reproductive organs, SPERMATOGENESIS; secondary male SEX CHARACTERISTICS; LIBIDO; development of muscle mass, strength, and power. Androgen,Androgen Receptor Agonist,Androgen Effect,Androgen Effects,Androgen Receptor Agonists,Androgenic Agents,Androgenic Compounds,Agents, Androgenic,Agonist, Androgen Receptor,Agonists, Androgen Receptor,Compounds, Androgenic,Effect, Androgen,Effects, Androgen,Receptor Agonist, Androgen,Receptor Agonists, Androgen
D000736 Androstenes Unsaturated derivatives of the steroid androstane containing at least one double bond at any site in any of the rings.
D000738 Androsterone A metabolite of TESTOSTERONE or ANDROSTENEDIONE with a 3-alpha-hydroxyl group and without the double bond. The 3-beta hydroxyl isomer is epiandrosterone. 3-alpha-Hydroxy-5-alpha-Androstan-17-One,5 alpha-Androstan-3 alpha-ol-17-one,Epiandrosterone,3 alpha Hydroxy 5 alpha Androstan 17 One,5 alpha Androstan 3 alpha ol 17 one
D013256 Steroids A group of polycyclic compounds closely related biochemically to TERPENES. They include cholesterol, numerous hormones, precursors of certain vitamins, bile acids, alcohols (STEROLS), and certain natural drugs and poisons. Steroids have a common nucleus, a fused, reduced 17-carbon atom ring system, cyclopentanoperhydrophenanthrene. Most steroids also have two methyl groups and an aliphatic side-chain attached to the nucleus. (From Hawley's Condensed Chemical Dictionary, 11th ed) Steroid,Catatoxic Steroids,Steroids, Catatoxic
D014556 Urine Liquid by-product of excretion produced in the kidneys, temporarily stored in the bladder until discharge through the URETHRA.

Related Publications

M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
The conjugated 17-hydroxy epimers of delta5-androstene-3beta-17-diol in infant and adult urine and umbilical cord plasma.
March 1968, Steroids,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
[Formation of 17 alpha-hydroxy-delta 5-pregnenolone and 3 beta-hydroxy-17-keto-delta 5-androstene (DHA) in adrenal and testicular tissue].
January 1961, Experientia,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Simple determination of 3alpha-hydroxy fraction and 3beta-hydroxy fraction of urinary 17-ketosteroids.
July 1976, Clinical chemistry,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Studies in steroid metabolism. XXXIV. Identification and characterization of 3-beta-hydroxy-delta 9(11)-androstene-17-one and 3beta, 11beta-dihydroxyandrostane-17-one from human urine.
September 1954, The Journal of biological chemistry,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
[A deep colored antimony compound from dehydroepiandrosterone (3beta-hydroxy-5-androstene-17-one). 79. Steroids and Sterines].
January 1977, Arzneimittel-Forschung,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Metabolism of 11 beta-hydroxy-delta 4-androstene-3, 17-dione in congenital adrenal hyperplasia.
December 1959, The Journal of clinical endocrinology and metabolism,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Structure-activity relationships in 4- and 5-androstene: 3beta-acetoxy-17-methyl-17-oxo-16,17-seco-5-androstene-16-carbonitrile and 17-methyl-3,17-dioxo-16,17-seco-4-androstene-16-carbonitrile.
September 2004, Acta crystallographica. Section C, Crystal structure communications,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Metabolism of delta 4-androstene-3beta, 17beta-diol and delta 4-androstene-3alpha, 17beta-diol in vitro.
January 1957, The Journal of biological chemistry,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
16-Substituted steroids. XVII. 5-Androstene-3beta, 16beta-diol and 5-androstene-3beta, 16alpha-diol.
September 1956, The Journal of biological chemistry,
M F JAYLE, and L G HUIS IN'T VELD, and E BAULIEU, and O CREPY
Synthesis of 7β-hydroxy-epiandrosterone.
January 2011, Steroids,
Copied contents to your clipboard!