Weight | 290.447 g/mol |
---|---|
Formula | C19H30O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
etiocholanolone (53-42-9)
Score:
#1062 in Biochemistry
,
#2748 in Biology
,
#3448 in Chemistry
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- Sigma-Aldrich - etiocholanolone76.80 - 161.00 USD
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- Comparison of agents producing a neutrophilic leukocytosis in man. Hydrocortisone, prednisone, endotoxin, and etiocholanolone. (Journal of Clinical Investigation, 1975)
- Changes in Human Serum Amyloid A and C-Reactive Protein after Etiocholanolone-Induced Inflammation (Journal of Clinical Investigation, 1978)
- Anticonvulsant Activity of Androsterone and Etiocholanolone (Epilepsia, 2005)
- Androgen responses to stress. II. Excretion of testosterone, epitestosterone, androsterone and etiocholanolone during basic combat training and under threat of attack. (Psychosomatic Medicine, 1969)
- Increased Granulocyte Collection with the Blood Cell Separator and the Addition of Etiocholanolone and Hydroxyethyl Starch (Transfusion, 1974)
- Effeets of etiocholanolone-indueed fever on plasma antipyrine half-lives and metabolie elearanee (Clinical Pharmacology & Therapeutics, 1975)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC12CCC(CC1CCC3C2CCC4(C3CCC4=O)C)O
-
InChIKeyQGXBDMJGAMFCBF-UHFFFAOYSA-N
- Pubchem - etiocholanolone
- Wikipedia - etiocholanolone
Etiocholanolone, also known as 5-androsterone, as well as 3-hydroxy-5-androstan-17-one or etiocholan-3-ol-17-one, is an etiocholane (5-androstane) steroid as well as an endogenous 17-ketosteroid that is produced from the metabolism of testosterone. It causes fever, immunostimulation, and leukocytosis, and is used to evaluate adrenal cortex function, bone marrow performance, and in neoplastic disease to stimulate the immune system. Etiocholanolone is also known to be an inhibitory androstane neurosteroid, acting as a positive allosteric modulator of the GABAA receptor, and possesses anticonvulsant effects.
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