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CP-1414S

Structure via PubChem · Public domain (PubChem)

EntityQ5013568· pop 7· linked from 539 articles

CP-1414S is an experimental drug first made by a team in Germany. It is a benzodiazepine derivative. CP-1414S is a 1,5-benzodiazepine, with the nitrogen atoms located at positions 1 and 5 of the diazepine ring, and so is most closely related to other 1,5-benzodiazepines such as clobazam.

In the Vinony graph

Vinony's link graph records 539 inbound references to CP-1414S, and connects out to benzodiazepine drug, alphenal and zapizolam.

It sits within the topics Chemical pages without DrugBank identifier, Drugboxes which contain changes to watched fields and Drugs not assigned an ATC code.

Vinony links it to 7 Wikipedia language editions.

Chemical data

Formula
C15H12N4O3
Molecular weight
296.28 g/mol
IUPAC name
4-amino-8-nitro-1-phenyl-3H-1,5-benzodiazepin-2-one
SMILES
C1C(=NC2=C(C=C(C=C2)[N+](=O)[O-])N(C1=O)C3=CC=CC=C3)N
InChIKey
MBSVPZTUXNRICW-UHFFFAOYSA-N
XLogP
1.4
Polar surface area
105 Ų
H-bond donors
1
H-bond acceptors
4
Formal charge
0

via PubChem

Wikidata facts

Mass
296.09094
Show 2 more facts
chemical formula
C₁₅H₁₂N₄O₃
canonical SMILES
C1C(=NC2=C(C=C(C=C2)[N+](=O)[O-])N(C1=O)C3=CC=CC=C3)N
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Encyclopedic overview

2 sections
Contents
  • See also
  • References

CP-1414S is an experimental drug first made by a team in Germany. It is a benzodiazepine derivative. CP-1414S is a 1,5-benzodiazepine, with the nitrogen atoms located at positions 1 and 5 of the diazepine ring, and so is most closely related to other 1,5-benzodiazepines such as clobazam.

CP-1414S has primarily anxiolytic and anticonvulsant effects. Its potency is roughly equal to that of clobazam, but with more pronounced sedation.

Excerpted from Wikipedia’s “CP-1414S” article, available under the CC BY-SA 4.0 licence.

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