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Ripazepam

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ripazepam
Identifiers
  • 1-ethyl-3-methyl-8-phenyl-4,6-dihydropyrazolo[4,3-e][1,4]diazepin-5-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H16N4O
Molar mass268.320 g·mol−1
3D model (JSmol)
  • CCN1C2=C(C(=N1)C)NC(=O)CN=C2C3=CC=CC=C3
  • InChI=1S/C15H16N4O/c1-3-19-15-13(10(2)18-19)17-12(20)9-16-14(15)11-7-5-4-6-8-11/h4-8H,3,9H2,1-2H3,(H,17,20) ☒N
  • Key:YFHYNLHGFKXAIQ-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Ripazepam is a pyrazolodiazepinone derivative structurally related to certainbenzodiazepine drugs, especiallyzolazepam. It hasanxiolytic effects.[1][2]

See also

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References

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  1. ^Fitzgerald JE, de la Iglesia FA, McGuire EJ (April 1984). "Carcinogenicity studies in rodents and ripazepam, a minor tranquilizing agent".Fundamental and Applied Toxicology.4 (2 Pt 1):178–90.doi:10.1016/0272-0590(84)90118-0.hdl:2027.42/24852.PMID 6724192.
  2. ^Baraldi PG, Manfredini S, Periotto V, Simoni D, Guarneri M, Borea PA (May 1985). "Synthesis and interaction of 5-(substituted-phenyl)-3-methyl-6,7-dihydropyrazolo[4,3-e] [1,4]diazepin-8(7H)-ones with benzodiazepine receptors in rat cerebral cortex".Journal of Medicinal Chemistry.28 (5):683–5.doi:10.1021/jm50001a025.PMID 2985787.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
Thienodiazepines
Thienotriazolodiazepines
Thienobenzodiazepines*
Pyridodiazepines
Pyridotriazolodiazepines
Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
Alcohols
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Kava constituents
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Nonbenzodiazepines
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