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Wikipedia

Ripazepam

Ripazepam is a pyrazolodiazepinone derivative structurally related to certain benzodiazepine drugs, especially zolazepam. It has anxiolytic effects.[1][2]

Ripazepam
Identifiers
  • 1-ethyl-3-methyl-8-phenyl-4,6-dihydropyrazolo[4,3-e][1,4]diazepin-5-one
CAS Number
  • 26308-28-1 Y
PubChem CID
  • 33474
ChemSpider
  • 30896 N
UNII
  • 92000WH9C9
KEGG
  • C19518 Y
ChEBI
  • CHEBI:82529
ChEMBL
  • ChEMBL159298 N
CompTox Dashboard (EPA)
  • DTXSID1021245
Chemical and physical data
FormulaC15H16N4O
Molar mass268.320 g·mol−1
3D model (JSmol)
  • Interactive image
  • 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
 NY (what is this?)  (verify)

See also

References

  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.

ripazepam, pyrazolodiazepinone, derivative, structurally, related, certain, benzodiazepine, drugs, especially, zolazepam, anxiolytic, effects, identifiersiupac, name, ethyl, methyl, phenyl, dihydropyrazolo, diazepin, onecas, number26308, ypubchem, cid33474chem. Ripazepam is a pyrazolodiazepinone derivative structurally related to certain benzodiazepine drugs especially zolazepam It has anxiolytic effects 1 2 RipazepamIdentifiersIUPAC name 1 ethyl 3 methyl 8 phenyl 4 6 dihydropyrazolo 4 3 e 1 4 diazepin 5 oneCAS Number26308 28 1 YPubChem CID33474ChemSpider30896 NUNII92000WH9C9KEGGC19518 YChEBICHEBI 82529ChEMBLChEMBL159298 NCompTox Dashboard EPA DTXSID1021245Chemical and physical dataFormulaC 15H 16N 4OMolar mass268 320 g mol 13D model JSmol Interactive imageSMILES CCN1C2 C C N1 C NC O CN C2C3 CC CC C3InChI 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 NKey YFHYNLHGFKXAIQ UHFFFAOYSA N N N Y what is this verify See also EditBenzodiazepineReferences Edit 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 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 This sedative related article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Ripazepam amp oldid 1122954028, wikipedia, wiki, book, books, library,

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