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.
|Animal models||Male Sprague–Dawley rats|
|Formulation||sterile doubly distilled water|
|Body Surface Area (m2)||0.007||0.025||0.15||0.05||0.02||0.5|
|Animal A (mg/kg) = Animal B (mg/kg) multiplied by||Animal B Km|
|Animal A Km|
For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 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 resveratrol of 11.2 mg/kg.
|Solubility||10 mM in DMSO|
Effect of cis-(Z)-flupentixol on DPPC membranes in the presence and absence of cholesterol.
Yonar D, et al. Chem Phys Lipids. 2016 Jun;198:61-71. PMID: 27282777.
The dopamine antagonist flupentixol does not alter ghrelin-induced food intake in rats.
Engster KM, et al. Neuropeptides. 2015 Oct;53:19-27. PMID: 26329764.
Wilforine is a sesquiterpene pyridine alkaloid; important bioactive compound in T. wilfordii plants, and is effective in treating idiopathic pulmonary fibrosis.
Wilfortrine is an immunomodulatory compound isolated from Tripterygium wilfordii.
Etanercept is a dimeric fusion protein consisting of two ligand-binding domains of human p75 tumor necrosis factor receptor and the human IgG1 Fc portion.
Tocilizumab is a humanized monoclonal antibody that binds to the interleukin-6 receptor, MW: 148 KD.
Lambrolizumabis a potent, highly selective, fully humanized immunoglobulin (Ig) G4-kappa monoclonal antibody against PD-1 with potential immune checkpoint inhibitory and antineoplastic activities. MW : 146.286 KD.
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