Vornorexant (ORN-0829; TS-142) is a potent dual OX1R and OX2R antagonist with IC 50 values of 1.05 nM and 1.27 nM, respectively. Vornorexant exhibits potent sleep-promoting effects? in vivo and can be used for insomnia research research In Vivo Vornorexant (oral administration; 1-10 mg/kg) exhibits potent sleep-promoting effects at a po. dose of 1 mg/kg in a rat polysomnogram study. It results in a dose-dependent increase in the percentage of total sleep . Vornorexant exhibits optimal PK properties with a rapid T max and short half-lives in rats and dogs. The T 1/2 is 0.238 hours and 1.16 hours, respectively in rat and dog . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Rat Dosage: 1, 3, 10 mg/kg Administration: Oral administration to rats prior to turning the light off (start of the active phase); 1-10 mg/kg Result: Possessed promising sleep-inducing and sleep-promoting effects. IC50& Target:OX 2 Receptor
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Vornorexant
CAS number:1517965-94-4(DMSO) molecular formula:C23H22FN7O2
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| Chinese alias | 沃诺雷生 | ||
| English alias | - | ||
| CAS number | 1517965-94-4(DMSO) | molecular formula | C23H22FN7O2 |
| molecular weight | 447.46 g/mol | Exact mass | 10mM in DMSO |
| PSA | - | logp | - |
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