Flubromazepam
From Infogalactic: the planetary knowledge core
Systematic (IUPAC) name | |
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7-Bromo-5-(2-fluorophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one
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Clinical data | |
Legal status |
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Routes of administration |
Oral |
Pharmacokinetic data | |
Biological half-life | 106 hours |
Identifiers | |
CAS Number | 2647-50-9 |
PubChem | CID: 12947024 |
ChemSpider | 10441497 |
UNII | GKX573279U |
Chemical data | |
Formula | C15H10BrFN2O |
Molecular mass | 333.16 g/mol |
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Flubromazepam is a benzodiazepine derivative which was first synthesized in 1960,[1] but was never marketed and did not receive any further attention or study until late 2012 when it appeared on the grey market as a novel designer drug.[2][3][4][5]
It is a structural analog of phenazepam in which the chlorine atom has been replaced by a fluorine atom.
An alternate isomer, 5-(2-bromophenyl)-7-fluoro-1,3-dihydro-2H-1,4-benzodiazepin-2-one, may have been sold under the same name.[2]
See also
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References
- ↑ US 3136815, "Amino substituted benzophenone oximes and derivatives thereof"
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Categories:
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- Benzodiazepines
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- GABAA receptor positive allosteric modulators
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