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meclonazepam

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EntityQ6804826· pop 11· linked from 542 articles

meclonazepam

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

In the Vinony graph

Within Vinony's link graph, meclonazepam is referenced by 542 other articles, and connects out to benzodiazepine drug, alphenal and zapizolam.

It sits within the topics 2-Chlorophenyl compounds, Chemical pages without DrugBank identifier and Designer drugs.

Its subject is documented across 10 Wikipedia language editions.

Chemical data

Formula
C16H12ClN3O3
Molecular weight
329.74 g/mol
IUPAC name
(3S)-5-(2-chlorophenyl)-3-methyl-7-nitro-1,3-dihydro-1,4-benzodiazepin-2-one

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
329.057
Show 4 more facts
chemical formula
C₁₆H₁₂ClN₃O₃
canonical SMILES
CC1C(=O)NC2=C(C=C(C=C2)[N+](=O)[O-])C(=N1)C3=CC=CC=C3Cl
isomeric SMILES
C[C@H]1C(=O)NC2=C(C=C(C=C2)[N+](=O)[O-])C(=N1)C3=CC=CC=C3Cl
Commons category
Meclonazepam
Sources (2)

via Wikidata · CC0

~2 min read

Encyclopedic overview

6 sections
Contents
  • Pharmacology
  • Legal issues
  • United Kingdom
  • See also
  • References
  • Further reading

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

Meclonazepam was never used as medicine and instead appeared online as a designer drug.

Excerpted from Wikipedia’s “meclonazepam” article, available under the CC BY-SA 4.0 licence.

Available in 10 languages

via Wikidata sitelinks · CC0

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