ChemicalBook--->CAS DataBase List--->167355-22-8

167355-22-8

167355-22-8 Structure

167355-22-8 Structure
IdentificationBack Directory
[Name]

Urea, N-phenyl-N'-[(3R)-2,3,4,5-tetrahydro-2,4-dioxo-1-phenyl-5-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-1H-1,5-benzodiazepin-3-yl]-
[CAS]

167355-22-8
[Synonyms]

GV150013
GV-150013
GV 150013
Urea, N-phenyl-N'-[(3R)-2,3,4,5-tetrahydro-2,4-dioxo-1-phenyl-5-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-1H-1,5-benzodiazepin-3-yl]-
[Molecular Formula]

C33H34N4O3
[MDL Number]

MFCD03106419
[MOL File]

167355-22-8.mol
[Molecular Weight]

534.65
Chemical PropertiesBack Directory
[Boiling point ]

792.3±60.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[pka]

9.56±0.20(Predicted)
Hazard InformationBack Directory
[Uses]

GV-150013 is a selective CCK-B receptor antagonist. GV-150013 has sleep aid effect[1].
[Definition]

ChEBI: GV 150013X is a benzodiazepine.
[in vivo]

GV-150013 (0.5 - 60μg/kg, ip, Once) increase REM sleep and non-REM sleep in old rats model[1].

Animal Model:Old rats [2].
Dosage:0.5 μg/kg, 5μg/kg, 60μg/kg
Administration:Intraperitoneal injection, Once
Result:The duration of REM sleep and non-REM sleep was longer than that of control.
[References]

[1] Crespi F. Cholecystokinin-B (CCK-B) receptor antagonists improve "aged" sleep: a new class of sleep modulators? Methods Find Exp Clin Pharmacol. 1999 Jan-Feb;21(1):31-8. DOI:10.1358/mf.1999.21.1.527016
[2] F.Crespi, et al. Influence of cholecystokinin-B (CCK-B) receptor antagonists on rat electroencephalography (EEG): A new class of sleep modulators? Gaviraghi. Dept of Pharmacology GlaxoWellcome S.p.A., Medicine Research Centre, via A. Fleming, 4, 37135 Verona, Italy
Spectrum DetailBack Directory
[Spectrum Detail]

Urea, N-phenyl-N'-[(3R)-2,3,4,5-tetrahydro-2,4-dioxo-1-phenyl-5-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-1H-1,5-benzodiazepin-3-yl]-(167355-22-8)1HNMR
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