| Weight | 332.484 g/mol |
|---|---|
| Formula | C21H32O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Alphaxalone (23930-19-0)
Score:
#940 in Neuroscience
,
#4121 in Biology
,
#5194 in Chemistry
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- Controlled Sedation with Alphaxalone-Alphadolone (BMJ, 1974)
- Modulation of GABAa receptor activity by alphaxalone (British Journal of Pharmacology, 1987)
- Differential antagonism by epipregnanolone of alphaxalone and pregnanolone potentiation of [3H]flunitrazepam binding suggests more than one class of binding site for steroids at GABAA receptors (Neuropharmacology, 1993)
- Differential subunit dependence of the actions of the general anesthetics alphaxalone and etomidate at gamma-aminobutyric acid type A receptors expressed in Xenopus laevis oocytes. (Molecular Pharmacology, 1997)
- Anxiolytic activity of steroid anesthetic alphaxalone. (Journal of Pharmacology and Experimental Therapeutics, 1991)
- PLASMA CONCENTRATIONS OF ALPHAXALONE DURING CONTINUOUS INFUSION OF ALTHESIN (BJA: British Journal of Anaesthesia, 1979)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)C1CCC2C1(CC(=O)C3C2CCC4C3(CCC(C4)O)C)C
-
InChIKeyDUHUCHOQIDJXAT-UHFFFAOYSA-N
- Pubchem - Alphaxalone
- Wikipedia - alfaxalone
Alfaxalone, also known as alphaxalone or alphaxolone, is a neuroactive steroid and general anesthetic. It is used in veterinary practice under the trade name Alfaxan as an induction agent for anesthesia and as an injectable anesthetic. Though it is more expensive than other induction agents, it often preferred due to the lack of depressive effects on the cardiovascular system.
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Alphaxalone
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