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SML0647

Sigma-Aldrich

Phenazepam

≥97% (HPLC)

Sinônimo(s):

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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About This Item

Fórmula empírica (Notação de Hill):
C15H10BrClN2O
Número CAS:
51753-57-2
Peso molecular:
349.61
Código UNSPSC:
12352200
NACRES:
NA.77

Nível de qualidade

100

Ensaio

≥97% (HPLC)

Formulário

powder

cor

white to beige

solubilidade

DMSO: 20 mg/mL, clear

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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)

chave InChI

CGMJQQJSWIRRRL-UHFFFAOYSA-N

Ações bioquímicas/fisiológicas

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.

Características e benefícios

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.

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Frases de perigo

H319,H340,H360,H362

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (COA)

Lot/Batch Number
053M4710V

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[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)
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
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
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

Artigos

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