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rilmazolam

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EntityQ98113711· pop 5· linked from 179 articles

rilmazolam

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Also known as CCRIS-1930, 8-chloro-6-(2-chlorophenyl)-N,N-dimethyl-4H-1,2,4-triazolo(1,5-a)(1,4)benzodiazepine-2-carboxamide

Rilmazolam, is a benzodiazepine derivative which acts as a sedative and hypnotic drug, and the active metabolite of the drug Rilmazafone. It has never been developed for medical uses, yet the aforementioned prodrug is an approved medication in Japan. It is primarily metabolized to desmethylrilmazolam, di-desmethylrilmazolam, and carboxy rilmazolam

In the Vinony graph

Vinony's link graph records 179 inbound references to rilmazolam, and connects out to benzodiazepine drug, zapizolam and Japan.

It is catalogued under topics including Chemical pages without ChemSpiderID, Chemical pages without DrugBank identifier and Drugs missing an ATC code.

Vinony links it to 4 Wikipedia language editions.

Chemical data

Formula
C19H15Cl2N5O
Molecular weight
400.3 g/mol
IUPAC name
8-chloro-6-(2-chlorophenyl)-N,N-dimethyl-4H-[1,2,4]triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide
SMILES
CN(C)C(=O)C1=NN2C(=N1)CN=C(C3=C2C=CC(=C3)Cl)C4=CC=CC=C4Cl
InChIKey
YMJXPUGNWIWFJI-UHFFFAOYSA-N
XLogP
3.8
Polar surface area
63.4 Ų
H-bond donors
0
H-bond acceptors
4
Formal charge
0

via PubChem

Wikidata facts

Mass
399.0653654600001
Show 3 more facts
canonical SMILES
CN(C)C(=O)C1=NN2C(=N1)CN=C(C3=C2C=CC(=C3)Cl)C4=CC=CC=C4Cl
chemical formula
C₁₉H₁₅Cl₂N₅O
Commons category
Rilmazafone metabolite

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • See also
  • References

Rilmazolam, is a benzodiazepine derivative which acts as a sedative and hypnotic drug, and the active metabolite of the drug Rilmazafone. It has never been developed for medical uses, yet the aforementioned prodrug is an approved medication in Japan. It is primarily metabolized to desmethylrilmazolam, di-desmethylrilmazolam, and carboxy rilmazolam

==See also== Flutazolam Etizolam Phenazepam Mexazolam Rilmazafone

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

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