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CP-1414S

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Chemical compound Pharmaceutical compound
CP-1414S
Clinical data
ATC code
  • none
Identifiers
IUPAC name
  • 1-phenyl-4-amino-8-nitro-3H-1,5-benzodiazepin-2-one
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H12N4O3
Molar mass296.286 g·mol
InChI
  • InChI=1S/C15H12N4O3/c16-14-9-15(20)18(10-4-2-1-3-5-10)13-8-11(19(21)22)6-7-12(13)17-14/h1-8H,9H2,(H2,16,17)
  • Key:MBSVPZTUXNRICW-UHFFFAOYSA-N
  (verify)

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.

See also

References

  1. US Patent 3766169 PROCESS FOR THE PREPARATION OF 3-AMINOMETHYLIDENE-1,5-BENZODIAZEPINE-2,4-(3H,5H)-DIONES
  2. Carli M, Ballabio M, Caccia S, Garattini S, Samanin R (1981). "Studies on some pharmacological activities of 7-nitro-2-amino-5-phenyl-3H-1,5-benzodiazepine (CP 1414 S) in the rat. A comparison with diazepam". Arzneimittel-Forschung. 31 (10): 1721–3. PMID 6119091.
  3. Mennini T, Garattini S (November 1982). "Benzodiazepine receptors': correlation with pharmacological responses in living animals". Life Sciences. 31 (19): 2025–35. doi:10.1016/0024-3205(82)90094-7. PMID 6129557.
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* atypical activity profile (not GABAA receptor ligands)
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See also: Receptor/signaling modulatorsGABA receptor modulatorsGABA metabolism/transport modulators


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