Cyprazepam
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| 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 |
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| 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  |
| 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 |
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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.
[edit] See also
[edit] 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.
- ^ "DHA-pharmaceutical agent conjugates - European Patent Application EP1466628". Patents online. 13 October 2004. 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]
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