Gidazepam
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Systematic (IUPAC) name | |
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2-(9-bromo- 3-oxo- 6-phenyl- 2,5-diazabicyclo [5.4.0] undeca- 5,8,10,12-tetraen- 2-yl) acetohydrazide | |
Clinical data | |
Pregnancy category |
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Routes of administration | Oral |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | Hepatic |
Biological half-life | ? |
Excretion | Renal |
Identifiers | |
CAS Number | 129186-29-4 |
ATC code | ?? (WHO) |
PubChem | CID 121919 |
DrugBank | ? |
Chemical data | |
Formula | C17H15BrN4O2 |
Molar mass | 387.2[[Script error: No such module "String".]] |
Gidazepam is a drug which is an atypical benzodiazepine derivative, developed in the Soviet Union.[1][2] It is a selectively anxiolytic benzodiazepine.[3] It also has therapeutic value in the management of certain cardiovascular disorders.[4][5][6][7][8]
Gidazepam is a prodrug for its active metabolite 7-bromo-5-phenyl-1,2-di-hydro-3H-1,4- benzodiazepine-2-one (desalkylgidazepam).[9][10] It is used as an antianxiety drug. Its anxiolytic effects can take several hours to manifest after dosing however, as it is the active metabolite which primarily gives the anxiolytic effects.[11]
See also
References
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- ↑ Petrova, TR; Tatarkin, AN (1994). "The neuroregulatory modulation of the hemodynamic reactions to physical loading in patients with cardiac arrhythmias". Terapevticheskii arkhiv. 66 (9): 65–8. ISSN 0040-3660. PMID 7992218.
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