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Gastrin/CCK antagonist 1

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Catalog No. T13260Cas No. 162271-52-5

Gastrin/CCK antagonist 1 is a potent gastrin/CCK antagonist for the study of metabolic system-related diseases.

Gastrin/CCK antagonist 1

Gastrin/CCK antagonist 1

😃Good
Purity: 98.33%
Catalog No. T13260Cas No. 162271-52-5
Gastrin/CCK antagonist 1 is a potent gastrin/CCK antagonist for the study of metabolic system-related diseases.
Pack SizePriceAvailabilityQuantity
1 mg665 €8-10 weeks
5 mg1.710 €8-10 weeks
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Purity:98.33%
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Product Introduction

Bioactivity
Description
Gastrin/CCK antagonist 1 is a potent gastrin/CCK antagonist for the study of metabolic system-related diseases.
Chemical Properties
Molecular Weight521.58
FormulaC28H32FN5O4
Cas No.162271-52-5
SmilesO=C(NC1=CC=C(F)C=C1)NC2C(=O)N(C=3C=CC=CC3N(C2=O)C4CCCCC4)CC(=O)N5CCCC5
Relative Density.1.37 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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