Ciclotizolam[1] (WE-973) is a drug which is a thienotriazolodiazepine derivative. It is a partial agonist for the benzodiazepine site of the GABAA receptor, with similar binding affinity to related compounds like brotizolam, but a low efficacy.[2][3]
Clinical data | |
---|---|
ATC code |
|
Legal status | |
Legal status |
|
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C20H18BrClN4S |
Molar mass | 461.81 g·mol−1 |
3D model (JSmol) | |
| |
| |
(what is this?) (verify) |
See also
editReferences
edit- ^ DE Patent 2445430
- ^ Weber KH, Kuhn FJ, Böke-Kuhn K, Lehr E, Danneberg PB, Hommer D, Paul SM, Skolnick P (February 1985). "Pharmacological and neurochemical properties of 1,4-diazepines with two annelated heterocycles ('hetrazepines')". European Journal of Pharmacology. 109 (1): 19–31. doi:10.1016/0014-2999(85)90535-7. PMID 2986988.19-31&rft.date=1985-02&rft_id=info:doi/10.1016/0014-2999(85)90535-7&rft_id=info:pmid/2986988&rft.aulast=Weber&rft.aufirst=KH&rft.au=Kuhn, FJ&rft.au=Böke-Kuhn, K&rft.au=Lehr, E&rft.au=Danneberg, PB&rft.au=Hommer, D&rft.au=Paul, SM&rft.au=Skolnick, P&rfr_id=info:sid/en.wikipedia.org:Ciclotizolam" class="Z3988">
- ^ Ikeda M, Weber KH, Bechtel WD, Malatynska E, Yamamura HI (1989). "Relative efficacies of 1,4-diazepines on GABA-stimulated chloride influx in rat brain vesicles". Life Sciences. 45 (4): 349–58. doi:10.1016/0024-3205(89)90145-8. PMID 2569655.349-58&rft.date=1989&rft_id=info:doi/10.1016/0024-3205(89)90145-8&rft_id=info:pmid/2569655&rft.aulast=Ikeda&rft.aufirst=M&rft.au=Weber, KH&rft.au=Bechtel, WD&rft.au=Malatynska, E&rft.au=Yamamura, HI&rfr_id=info:sid/en.wikipedia.org:Ciclotizolam" class="Z3988">