| Weight | 300.398 g/mol |
|---|---|
| Formula | C19H24O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
ADRENOSTERONE (911474-75-4, 382-45-6)
11-ketoandrostenedione · adrenosterone, 3H-labeled · 4-androstene-3,11,17-trione
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- Androgen and Behavior in the Male Three-Spined Stickleback, Gasterosteus aculeatus: II. Castration and 11-Ketoandrostenedione Effects on Courtship and Parental Care during the Nesting Cycle (Hormones and Behavior, 2002)
- Conversion of 11-ketoandrostenedione to 11-ketotestosterone by blood cells of six fish species (General and Comparative Endocrinology, 1990)
- Stereochemical control of intramolecular conjugate addition. A short, highly stereoselective synthesis of adrenosterone (Journal of the American Chemical Society, 1982)
- Treatment of GnRHa-implanted Senegalese sole (Solea senegalensis) with 11-ketoandrostenedione stimulates spermatogenesis and increases sperm motility. (Comparative Biochemistry and Physiology A-molecular & Integrative Physiology, 2007)
- Biotransformation of adrenosterone by filamentous fungus, Cunninghamella elegans (Steroids, 2007)
- Stimulation of Spawning Behavior in Castrated Rainbow Trout (Oncorhynchus mykiss) by 17, 20-Dihydroxy-4-pregnen-3-one, but Not by 11-Ketoandrostenedione (Hormones and Behavior, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 11-ketoandrostenedione
- adrenosterone, 3H-labeled
- 4-androstene-3,11,17-trione
-
SMILESCC12CCC(=O)C=C1CCC3C2C(=O)CC4(C3CCC4=O)C
-
InChIKeyRZRPTBIGEANTGU-UHFFFAOYSA-N
- Pubchem - ADRENOSTERONE
- Wikipedia - adrenosterone
Adrenosterone, also known as Reichstein's substance G , as well as 11-ketoandrostenedione (11-KA4), 11-oxoandrostenedione (11-OXO), and androst-4-ene-3,11,17-trione, is a steroid hormone with a weak androgenic effect, and an intermediate/prohormone of 11-ketotestosterone. It was first isolated in 1936 from the adrenal cortex by Tadeus Reichstein at the Pharmaceutical Institute in the University of Basel. Originally, adrenosterone was called Reichstein's substance G.
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