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Merck
CN

SML0647

Sigma-Aldrich

芬那西泮标准液

≥97% (HPLC)

别名:

7-Bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one, 7-Bromo-5-(2-chlorophenyl)-1,3-dihydrobenzo[e]-1,4-diazepin-2-one, BD 98, Fenazepam

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关于此项目

经验公式（希尔记法）:
C15H10BrClN2O
化学文摘社编号:
51753-57-2
分子量:
349.61
UNSPSC代码:
12352200
NACRES:
NA.77

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质量水平

100

方案

≥97% (HPLC)

表单

powder

drug control

Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet

颜色

white to beige

溶解性

DMSO: 20 mg/mL, clear

储存温度

−20°C

SMILES字符串

Brc1cc2c(cc1)NC(=O)CN=C2c3c(cccc3)Cl

InChI

1S/C15H10BrClN2O/c16-9-5-6-13-11(7-9)15(18-8-14(20)19-13)10-3-1-2-4-12(10)17/h1-7H,8H2,(H,19,20)

InChI key

CGMJQQJSWIRRRL-UHFFFAOYSA-N

生化/生理作用

Phenazepam is an agonist of the γ-Aminobutyric acid A (GABAA)-benzodiazepine receptor chloride channel complex.
Phenazepam is the benzodiazepine that exhibit anticonvulsive, anxiolytic, sedative and hypnotic effects in humans and experimental animals. Phenazepam is an agonist of the γ-Aminobutyric acid A (GABAA)-benzodiazepine receptor chloride channel complex.

特点和优势

This compound is featured on the GABAA Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

象形图

Health hazardExclamation mark
GHS08,GHS07

警示用语：

Danger

危险分类

Eye Irrit. 2 - Lact. - Muta. 1B - Repr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000027975
053M4710V

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N Ia Golovenko et al.
Farmakologiia i toksikologiia, 43(2), 144-148 (1980-03-01)
The distribution pattern of 14C-phenazepam and some of its metabolites in the liver, brain and blood plasma at a prolonged (45 days) administration to rats does not differ from that after a single administration. The liver and brain demonstrated an
Peter D Maskell et al.
Journal of forensic and legal medicine, 19(3), 122-125 (2012-03-07)
In the past few years there has been concern in Western Europe and in the US about the rise in abuse of phenazepam, a benzodiazepine that was originally developed in the USSR in the mid- to late 1970s.(1-4) Although phenazepam
[Evaluation of the effect of phenazepam and seduxen on the functional state of the cardiovascular system in the acute phase of an infarct].
G Lukhanana
Vrachebnoe delo, (10)(10), 15-18 (1983-10-01)
John Martin Corkery et al.
Human psychopharmacology, 27(3), 254-261 (2012-03-13)
Phenazepam (fenazepam; 7-bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one; PNZ, 'Bonsai') is a benzodiazepine developed in the former Soviet Union during the 1970s to treat neurological disorders, epilepsy, and alcohol withdrawal syndrome. Its recreational use appears to have increased over recent years. Because of the lack
Jon B Stephenson et al.
Journal of analytical toxicology, 37(1), 25-29 (2012-10-18)
Phenazepam use in the state of Georgia has increasingly become a trend for a drug market looking at new and different recreational drugs. This paper examines the psychomotor effects of phenazepam on individuals and their ability to operate a motor

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