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nitemazepam

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EntityQ62014635· pop 5· linked from 409 articles

nitemazepam

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Nitemazepam (or 3-hydroxynimetazepam) is a benzodiazepine derivative which was first synthesised in the 1970s but was never marketed. It is the 7-nitro instead of 7-chloro analogue of temazepam, and also the 3-hydroxy derivative of nimetazepam, and an active metabolite. It has in more recent years been sold as a designer drug, first being definitively identified in Europe in 2017. It is metabolized to 7-aminonitemazepam, nimetazepam, 3-hydroxynitemazepam, temazepam, and nimetazepam glucuronide.

In the Vinony graph

Within Vinony's link graph, nitemazepam is referenced by 409 other articles, and connects out to benzodiazepine drug, allopregnanolone and isovaleric acid.

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

Its subject is documented across 5 Wikipedia language editions.

Chemical data

Formula
C16H13N3O4
Molecular weight
311.29 g/mol
IUPAC name
3-hydroxy-1-methyl-7-nitro-5-phenyl-3H-1,4-benzodiazepin-2-one
SMILES
CN1C2=C(C=C(C=C2)[N+](=O)[O-])C(=NC(C1=O)O)C3=CC=CC=C3
InChIKey
QRWVNMAJJIQCEG-UHFFFAOYSA-N
XLogP
1.4
Polar surface area
98.7 Ų
H-bond donors
1
H-bond acceptors
5
Formal charge
0

via PubChem

Wikidata facts

Show 2 more facts
different from
nitrazepam
subject has role
benzodiazepine drug
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via Wikidata · CC0

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Encyclopedic overview

1 sections
Contents
  • References

Nitemazepam (or 3-hydroxynimetazepam) is a benzodiazepine derivative which was first synthesised in the 1970s but was never marketed. It is the 7-nitro instead of 7-chloro analogue of temazepam, and also the 3-hydroxy derivative of nimetazepam, and an active metabolite. It has in more recent years been sold as a designer drug, first being definitively identified in Europe in 2017. It is metabolized to 7-aminonitemazepam, nimetazepam, 3-hydroxynitemazepam, temazepam, and nimetazepam glucuronide.

==References==

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

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