Weight | 257.377 g/mol |
---|---|
Formula | C17H23NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
DEXTRORPHAN (297-90-5, 125-73-5)
(+-)-17-Methylmorphinan-3-ol
Score:
#205 in Neurology
,
#909 in Neuroscience
,
#1846 in Biochemistry
,
#3992 in Biology
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- Intrathecal treatment with dextrorphan or ketamine potently reduces pain-related behaviors in a rat model of peripheral mononeuropathy (Brain Research, 1993)
- Safety, Tolerability, and Pharmacokinetics of the N-Methyl-d-Aspartate Antagonist Dextrorphan in Patients With Acute Stroke (Stroke, 1995)
- Dextrorphan and dextromethorphan attenuate glutamate neurotoxicity (Brain Research, 1987)
- Dextrorphan and levorphanol selectively block N-methyl-D-aspartate receptor-mediated neurotoxicity on cortical neurons. (Journal of Pharmacology and Experimental Therapeutics, 1987)
- Differential effects of dextrorphan and levorphanol on the excitation of rat spinal neurons by amino acids. (European Journal of Pharmacology, 1985)
- Dextrorphan relieves neuropathic heat-evoked hyperalgesia in the rat (Neuroscience Letters, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - (+-)-17-Methylmorphinan-3-ol
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SMILESCN1CCC23CCCCC2C1CC4=C3C=C(C=C4)O
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InChIKeyJAQUASYNZVUNQP-UHFFFAOYSA-N
- Pubchem - DEXTRORPHAN
- Wikipedia - dextrorphan
Dextrorphan (DXO) is a psychoactive drug of the morphinan class which acts as an antitussive or cough suppressant and dissociative hallucinogen. It is the dextrorotatory-stereoisomer of racemorphan, the levo-half being levorphanol. Dextrorphan is produced by O-demethylation of dextromethorphan by CYP2D6.
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