The dopamine antagonist, Fupentixol did not affect the ghrelin-induced food intake. During the first half of the dark phase Fupentixol significantly increased the intake of standard chow, whereas a decrease in food intake was observed during the second part of the dark phase.
Cell Experiment | |
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Cell lines | |
Preparation method | |
Concentrations | |
Incubation time |
Animal Experiment | |
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Animal models | Male Sprague–Dawley rats |
Formulation | sterile doubly distilled water |
Dosages | 0.25 mg/kg |
Administration | i.p. |
Molecular Weight | 507.44 |
Formula | C23H27Cl2F3N2OS |
CAS Number | 2413-38-9 |
Form | Solid |
Solubility (25°C) | 10 mM in DMSO |
Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
Species | Mouse | Rat | Rabbit | Guinea pig | Hamster | Dog |
Weight (kg) | 0.02 | 0.15 | 1.8 | 0.4 | 0.08 | 10 |
Body Surface Area (m2) | 0.007 | 0.025 | 0.15 | 0.05 | 0.02 | 0.5 |
Km factor | 3 | 6 | 12 | 8 | 5 | 20 |
Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
Animal A Km |
For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.
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