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SNT-207858 free base

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Catalog No. T12945Cas No. 1104662-66-9

SNT-207858 free base is a selective, blood brain barrier penetrating, potent and orally active antagonist of melanocortin-4 (MC-4) receptor(IC50 of 22 nM (binding) and 11 nM (function), on the MC-4 receptor).

SNT-207858 free base

SNT-207858 free base

😃Good
Catalog No. T12945Cas No. 1104662-66-9
SNT-207858 free base is a selective, blood brain barrier penetrating, potent and orally active antagonist of melanocortin-4 (MC-4) receptor(IC50 of 22 nM (binding) and 11 nM (function), on the MC-4 receptor).
Pack SizePriceAvailabilityQuantity
5 mg$4466-8 weeks
25 mg$1,4306-8 weeks
50 mg$1,8606-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
SNT-207858 free base is a selective, blood brain barrier penetrating, potent and orally active antagonist of melanocortin-4 (MC-4) receptor(IC50 of 22 nM (binding) and 11 nM (function), on the MC-4 receptor).
In vitro
SNT207858 exhibits binding affinity to the MC-4 receptor at 22 nM, demonstrating significant selectivity with a 170-fold preference compared to MC-3 and a 40-fold preference over MC-5.
In vivo
In mice,the tumor induced weight loss significantly reduced by SNT207858 (30 mg/kg; oral administration; once daily; 15 days).
Chemical Properties
Molecular Weight616.62
FormulaC32H43Cl2N5O3
Cas No.1104662-66-9
Relative Density.1.258 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 125 mg/mL (202.72 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6217 mL8.1087 mL16.2174 mL81.0872 mL
5 mM0.3243 mL1.6217 mL3.2435 mL16.2174 mL
10 mM0.1622 mL0.8109 mL1.6217 mL8.1087 mL
20 mM0.0811 mL0.4054 mL0.8109 mL4.0544 mL
50 mM0.0324 mL0.1622 mL0.3243 mL1.6217 mL
100 mM0.0162 mL0.0811 mL0.1622 mL0.8109 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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