Methylmethaqualone
| Systematic (IUPAC) name | |
|---|---|
| 3-(2,4-dimethylphenyl)-2-methylquinazolin-4(3H)-one | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 3244-75-5 |
| ATC code | None |
| PubChem | CID 63382 |
| ChemSpider | 57045 |
| Chemical data | |
| Formula | C17H16N2O |
| Mol. mass | 264.322 |
| SMILES | eMolecules & PubChem |
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Methylmethaqualone (MMQ) is an analogue of methaqualone which has similar sedative and hypnotic properties to its parent compound, and is around the same potency. Methylmethaqualone differs from methaqualone by 4-methylation on the phenyl ring. It was made illegal in Germany in 1999 and listed by the DEA as a "drug of forensic interest" at about the same time, but little other information is available, it would appear that this compound was sold on the black market in Germany as a designer drug analogue of methaqualone.[1][2]
Animal studies of methylmethaqualone have shown it to produce convulsions at only slightly above the effective sedative dose,[3] and anecdotal reports from human users have confirmed that it can have a pro-convulsive effect, which could potentially make this compound particularly hazardous if taken in excessive doses.
[edit] References
- ^ Klein RFX, Hays PA (January–June; 2003). "Detection and Analysis of Drugs of Forensic Interest, 1992 - 2001; A Literature Review." (pdf). Microgram Journal (DEA) 1 (1–2): 60. http://www.justice.gov/dea/programs/forensicsci/microgram/journal_v1/2003_1-2.pdf.
- ^ Angelos, S. A.; Lankin, D. C.; Meyers, J. A.; Raney, J. K. (1993). "The structural identification of a methyl analog of methaqualone via 2-dimensional NMR techniques". Journal of forensic sciences 38 (2): 455–465. PMID 8455002.
- ^ Boltze, K. H.; Dell, H. D.; Lehwald, H.; Lorenz, D.; Rueberg-Schweer, M. (1963). "Substituted 4-Quinazolinone Derivatives As Hypnotics and Anticonvulsants". Arzneimittel-Forschung 13: 688–701. PMID 14085923.
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