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 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 animals exhibit slightly higher baseline mean arterial blood pressure values than controls. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:Orexin 1 receptor
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GSK1059865
CAS number:1191044-58-2 molecular formula:C20H23BrFN3O2
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 1191044-58-2 | molecular formula | C20H23BrFN3O2 |
| molecular weight | 436.33 g/mol | Exact mass | ≥99% |
| PSA | 54.500 Ų | logp | 4.400 |
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