Methylmethaqualone

Methylmethaqualone
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 YesY
Chemical data
Formula C17H16N2O 
Mol. mass 264.322
SMILES eMolecules & PubChem
 YesY(what is this?)  (verify)

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.

References

  1. ^ 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. 
  2. ^ 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.  edit
  3. ^ 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.  edit