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-imine
Clinical 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 Y
ATC code	None
PubChem	CID 27452
ChemSpider	16736916 Y
UNII	933N61G4SL Y
KEGG	D03631 Y
Chemical data
Formula	C19H18ClN3O
Mol. mass	339.819 g/mol
SMILES	eMolecules & PubChem
InChI InChI=1S/C19H18ClN3O/c20-15-8-9-17-16(10-15)19(14-4-2-1-3-5-14)23(24)12-18(22-17)21-11-13-6-7-13/h1-5,8-10,13H,6-7,11-12H2,(H,21,22) Y Key:UKFDTMNJMKWWNK-UHFFFAOYSA-N Y
Y(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

• Benzodiazepine

References

1. ^ US Patent 3138586
2. ^ 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. 
3. ^ 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. 
4. ^ "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. 
5. ^ 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. 
6. ^ 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]}

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