| Weight | 353.506 g/mol |
|---|---|
| Formula | C23H31NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 8 |
Levomethadyl acetate (1477-40-3)
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- A comparison of levomethadyl acetate, buprenorphine, and methadone for opioid dependence. (The New England Journal of Medicine, 2000)
- Torsades de Pointes Associated with High Dose Levomethadyl Acetate (ORLAAM (Journal of Addictive Diseases, 2001)
- Dose-related efficacy of levomethadyl acetate for treatment of opioid dependence: A randomized clinical trial (JAMA, 1997)
- Levomethadyl Acetate: Prolonged Duration of Opioid Effects, Including Cross Tolerance to Heroin, in Man (JAMA, 1973)
- HIV risk behaviors during pharmacologic treatment for opioid dependence: A comparison of levomethadyl acetate hydrochloride, buprenorphine, and methadone (Journal of Substance Abuse Treatment, 2006)
- Induction With Levomethadyl Acetate: Safety and Efficacy (Archives of General Psychiatry, 1998)
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SMILESCCC(C(CC(C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2)OC(=O)C
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- Pubchem - Levomethadyl acetate
- Wikipedia - levomethadyl acetate
Levacetylmethadol (INN), levomethadyl acetate (USAN), OrLAAM (trade name) or levo--acetylmethadol (LAAM) is a synthetic opioid similar in structure to methadone. It has a long duration of action due to its active metabolites. It was approved in 1993 by the U.S.
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