- Cyprazepam
-
Cyprazepam Systematic (IUPAC) name 10-chloro-N-(cyclopropylmethyl)-3-hydroxy-2-phenyl-
3,6-diazabicyclo[5.4.0]undeca-1,6,8,10-tetraen-5-imineClinical data Pregnancy cat. ? Legal status Schedule IV(US) Routes Oral Pharmacokinetic data Bioavailability ? Metabolism Hepatic Half-life ? Excretion Renal Identifiers CAS number 15687-07-7 ATC code None PubChem CID 27452 ChemSpider 16736916 UNII 933N61G4SL KEGG D03631 Chemical data Formula C19H18ClN3O Mol. mass 339.819 g/mol SMILES eMolecules & PubChem (what is this?) (verify) Cyprazepam[1] is a drug which is a sedative-hypnotic benzodiazepine derivative.[2][3][4][5] It has anxiolytic properties,[6] and presumably also has hypnotic, skeletal muscle relaxant, anticonvulsant and amnestic properties.
See also
References
- ^ US Patent 3138586
- ^ Herbert Oelschläger; Doris Martienssen, F. Belal (22 September 2006). "Ring Contraction of 1,4-Benzodiazepines to 3,4-Dihydroquinazolines During Macro Scale Reduction (Example 5: Cyprazepam)". Archiv der Pharmazie (Wiley Interscience) 325 (8): 503–507. doi:10.1002/ardp.19923250810. ISSN 0365-6233. http://www3.interscience.wiley.com/journal/113348763/abstract.
- ^ Bradley Matthews; Shashoua Victor, Webb Nigel, Swindell Charles (13 October 2004). "DHA-pharmaceutical agent conjugates - European Patent Application EP1466628". Patents online. http://www.freepatentsonline.com/EP1466628.html. Retrieved 19 September 2009.
- ^ "Harmonized Tariff Schedule of the United States (2009) - Supplement 1 - PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE" (PDF). USA: United States International Trade Commission. 2009. http://www.usitc.gov/publications/docs/tata/hts/bychapter/0910PHARMAPPX.pdf. Retrieved 19 September 2009.
- ^ E. W. Schafer; Jr W. A. Bowles, Jr, J. Hurlbut (1983). "The Acute Oral Toxicity, Repellency, and Hazard Potential of 998 Chemicals to One or More Species of Wild and Domestic Birds" (PDF). Arch. Environm. Contam. Toxicol (USA) 12 (3): 355–382. doi:10.1007/BF01059413. PMID 6882015. http://www.springerlink.com/content/q3r47rn103727752/fulltext.pdf. Retrieved 19 September 2009.
- ^ World Health Organisation (2006). "The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances" (PDF). USA: Minstry of health, Syria. http://www.moh.gov.sy/Pages/DrugAndNutrition/documents/INN%20Stems/RevisedFinalStemBook2006.pdf. Retrieved 19 September 2009.[dead link]
Benzodiazepine derivatives 1,4-Benzodiazepines Bromazepam · Camazepam · Carburazepam · Chlordiazepoxide · Cinolazepam · Clonazepam · Clorazepate · Cyprazepam · Delorazepam · Demoxepam · Devazepide * · Diazepam · Doxefazepam · Elfazepam · Ethyl carfluzepate · Ethyl dirazepate · Ethyl loflazepate · Fletazepam · Fludiazepam · Flunitrazepam · Flurazepam · Flutemazepam · Flutoprazepam · Fosazepam · Gidazepam · Halazepam · Iclazepam · Ketazolam · Lorazepam · Lormetazepam · Meclonazepam · Medazepam · Menitrazepam · Metaclazepam · Motrazepam · Nimetazepam · Nitrazepam · Nitrazepate · Nordazepam · Nortetrazepam · Oxazepam · Phenazepam · Pinazepam · Pivoxazepam · Prazepam · Proflazepam · Quazepam · QH-II-66 · Reclazepam · Ro5-2904 · Ro5-4864 * · Sulazepam · Temazepam · Tetrazepam · Tifluadom * · Tolufazepam · Tuclazepam · Uldazepam
1,5-Benzodiazepines Arfendazam · Clobazam · CP-1414S · Lofendazam · Triflubazam
2,3-Benzodiazepines * Girisopam · GYKI-52466 · GYKI-52895 · Nerisopam · Talampanel · Tofisopam
Triazolobenzodiazepines Adinazolam · Alprazolam · Estazolam · Flubromazolam · Triazolam
Imidazobenzodiazepines Bretazenil · Climazolam · FG-8205 · Flumazenil · Imidazenil · L-655,708 · Loprazolam · Midazolam · PWZ-029 · Remimazolam · Ro15-4513 · Ro48-6791 · Ro48-8684 · Sarmazenil · SH-053-R-CH3-2′F
Oxazolobenzodiazepines Cloxazolam · Flutazolam · Haloxazolam · Mexazolam · Oxazolam
Thienodiazepines Bentazepam · Brotizolam · Ciclotizolam · Clotiazepam · Etizolam · Olanzapine *
Pyridodiazepines Lopirazepam · Zapizolam
Pyrazolodiazepines Pyrrolodiazepines Tetrahydroisoquinobenzodiazepines Benzodiazepine prodrugs * atypical activity profile (not GABAA receptor ligands)This pharmacology-related article is a stub. You can help Wikipedia by expanding it.