Weight | 309.453 g/mol |
---|---|
Formula | C21H27NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 7 |
Isomethadone (466-40-0)
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- Identification and quantitative determination of some metabolites of methadone, isomethadone and normethadone. (Journal of Pharmacy and Pharmacology, 1971)
- The Synthesis of Isomethadone (Journal of the American Chemical Society, 1952)
- ANALGESIC POTENCY AND SIDE ACTION LIABILITY IN MAN OF HEPTAZONE, WIN 1161-2, 6-METHYL DIHYDROMORPHINE, METOPON, LEVO-ISOMETHADONE AND PENTOBARBITAL SODIUM, AS A FURTHER EFFORT TO REFINE METHODS OF EVALUATION OF ANALGESIC DRUGS (Journal of Pharmacology and Experimental Therapeutics, 1952)
- Stereochemical studies on medicinal agents. 16. Conformational studies of methadone and isomethadone utilizing circular dichroism and proton magnetic resonance (Journal of Medicinal Chemistry, 1974)
- Resolution ofdl-Methadone anddl-Isomethadone (Journal of the American Chemical Society, 1949)
- Antitussive Action of d-Isomethadone and d-Methadone in Dogs (Experimental Biology and Medicine, 1952)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC(=O)C(C1=CC=CC=C1)(C2=CC=CC=C2)C(C)CN(C)C
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InChIKeyIFKPLJWIEQBPGG-UHFFFAOYSA-N
- Pubchem - Isomethadone
- Wikipedia - isomethadone
Isomethadone (INN, BAN; Liden), also known as isoamidone, is a synthetic opioid analgesic and antitussive related to methadone that was used formerly as a pharmaceutical drug but is now no longer marketed. Isomethadone was used as both an analgesic and antitussive. It binds to and activates both the - and -opioid receptors, with the (S)-isomer being the more potent of its two enantiomers.
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