Meclonazepam

Meclonazepam
Clinical data
ATC code none
Legal status
Legal status
Identifiers
CAS Number 58662-84-3 N
PubChem (CID) 3033985
ChemSpider 2298544 YesY
UNII RN43209SMA YesY
ChEMBL CHEMBL351821 N
Chemical and physical data
Formula C16H12ClN3O3
Molar mass 329.74 g/mol
3D model (Jmol) Interactive image
 NYesY (what is this?)  (verify)

Meclonazepam[1] ((S)-3-methylclonazepam) was discovered by a team at Hoffmann-La Roche in the 1970s and is a drug which is a benzodiazepine derivative similar in structure to clonazepam.[2] It has sedative and anxiolytic actions like those of other benzodiazepines,[3] and also has anti-parasitic effects against the parasitic worm Schistosoma mansoni.[4]

Meclonazepam was never used as medicine and instead appeared online as a designer drug.[5][6]

See also

References

  1. U.S. Patent 4,031,078
  2. The Lundbeck Institute. "Meclonazepam". Psychotropics. Lundbeck.
  3. Ansseau, M.; Doumont, A.; Thiry, D.; Von Frenckell, R.; Collard, J. (1985). "Initial study of methylclonazepam in generalized anxiety disorder. Evidence for greater power in the cross-over design". Psychopharmacology. 87 (2): 130–135. doi:10.1007/bf00431795. PMID 3931136.
  4. O'Boyle, C.; Lambe, R.; Darragh, A. (1985). "Central Effects in Man of the Novel Schistosomicidal Benzodiazepine Meclonazepam". European Journal of Clinical Pharmacology. 29 (1): 105–108. doi:10.1007/bf00547377. PMID 4054198.
  5. Markus R. Meyer; Madeleine Pettersson Bergstrand; Anders Helander; Olof Beck (May 2016). "Identification of main human urinary metabolites of the designer nitrobenzodiazepines clonazolam, meclonazepam, and nifoxipam by nano-liquid chromatography-high-resolution mass spectrometry for drug testing purposes". Analytical and Bioanalytical Chemistry. 408 (13): 3571–3591. doi:10.1007/s00216-016-9439-6. PMID 27071765.
  6. Pettersson Bergstrand M, Helander A, Hansson T, Beck O (2016). "Detectability of designer benzodiazepines in CEDIA, EMIT II Plus, HEIA, and KIMS II immunochemical screening assays". Drug Test Anal. doi:10.1002/dta.2003. PMID 27366870.

Further reading


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