ChemicalBook--->CAS DataBase List--->1191044-58-2

1191044-58-2

1191044-58-2 Structure

1191044-58-2 Structure
IdentificationBack Directory
[Name]

GSK1059865
[CAS]

1191044-58-2
[Synonyms]

GSK1059865
GSK-1059865 (GSK 1059865
Methanone, [(2S,5S)-2-[[(5-bromo-2-pyridinyl)amino]methyl]-5-methyl-1-piperidinyl](3-fluoro-2-methoxyphenyl)-
[Molecular Formula]

C20H23BrFN3O2
[MDL Number]

MFCD31618413
[MOL File]

1191044-58-2.mol
[Molecular Weight]

436.32
Chemical PropertiesBack Directory
[Boiling point ]

575.8±50.0 °C(Predicted)
[density ]

1.376±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : ≥ 50 mg/mL (114.59 mM)
[form ]

Solid
[pka]

4.89±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Biological Activity]

GSK1059865 is a potent orexin 1 receptor antagonist.
[in vivo]

Treatment with GSK1059865 significantly decreases ethanol drinking in a dose-dependent manner in CIE-exposed mice. In contrast GSK1059865 decreases drinking in air-exposed mice only at the highest dose used. There is no effect of GSK1059865 on sucrose intake. GSK1059865 (0.3 nM-10 nM) produces non-surmountable antagonism with a dose-dependent rightward shift of the OXA EC 50 and a concomitant decrease of the agonist maximal response. The calculated pK B value is 8.77±0.12 for GSK1059865. GSK1059865 (0.1-3.3 μM) produces a classical surmountable profile with parallel rightward shift of the OXA EC 50 without depression of the agonist maximal response. Intraperitoneal The administration of GSK1059865 produces a region-dependent inhibition of yohimbine-induced relative cerebral blood volume response. The administration of GSK1059865 per se produces a weak relative cerebral blood volume increase in several brain regions. GSK1059865-pretreated ani mals exhibit slightly higher baseline mean arterial blood pressure values than controls.

[target]

Orexin 1 receptor

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