Fletazepam
 | |
| Clinical data | |
|---|---|
| ATC code |
|
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ECHA InfoCard | 100.047.309 |
| Chemical and physical data | |
| Formula | C17H13ClF4N2 |
| Molar mass | 356.745 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
Fletazepam[1] is a drug which is a benzodiazepine derivative. It has sedative and anxiolytic effects similar to those produced by other benzodiazepine derivatives, but is mainly notable for its strong muscle relaxant properties.[2]
Fletazepam is most closely related to other N-trifluoroethyl substituted benzodiazepines such as halazepam and quazepam.[3]
See also
References
- ↑ DE 2106175
- ↑ Barnett, A.; Goldstein, J.; Fiedler, EP.; Taber, RI. (Nov 1974). "The pharmacology of fletazepam a centrally-acting muscle relaxant.". Arch Int Pharmacodyn Ther. 212 (1): 164–74. PMID 4476200.
- ↑ Iorio, LC.; Barnett, A.; Billard, W. (Jul 1984). "Selective affinity of 1-N-trifluoroethyl benzodiazepines for cerebellar type 1 receptor sites.". Life Sci. 35 (1): 105–13. PMID 6738302. doi:10.1016/0024-3205(84)90157-7.
This article is issued from
Wikipedia.
The text is licensed under Creative Commons - Attribution - Sharealike.
Additional terms may apply for the media files.