Brotizolam
A thienodiazepine drug with sedative, hypnotic, and anxiolytic properties, used in some countries for the short-term treatment of insomnia and anxiety. It acts on GABA-A receptors similarly to benzodiazepines to promote sleep and reduce anxiety. Risk of tolerance, dependence, and withdrawal limits its use to short-term treatment.
分子量
393.7000 g/mol
LogP
2.80
TPSA
71.30 Ų
Lipinski 五规则
符合
治疗领域
作用机制
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, and anticonvulsant effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, …
二维结构
Cite this structure
Embed this structure
SMILES
Cc1nnc2n1-c1sc(Br)cc1C(c1ccccc1Cl)=NC2
InChI
InChI=1S/C15H10BrClN4S/c1-8-19-20-13-7-18-14(9-4-2-3-5-11(9)17)10-6-12(16)22-15(10)21(8)13/h2-6H,7H2,1H3
Molecular Formula
C15H10BrClN4S
HBD / HBA
- / 4
可旋转键数
1
重原子数
22
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
常见问题
A thienodiazepine drug with sedative, hypnotic, and anxiolytic properties, used in some countries for the short-term treatment of insomnia and anxiety. It acts on GABA-A receptors similarly to benzodiazepines to promote sleep and reduce anxiety. Risk of tolerance, dependence, and withdrawal limits its use to short-term treatment.
Enhances the effect of gamma-aminobutyric acid (GABA) at GABA-A receptors by binding to an allosteric site and increasing the frequency of chloride ion channel opening. This produces anxiolytic, sedative, hypnotic, and anticonvulsant effects.
Yes, Brotizolam is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL32479. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2451. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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