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FAUC 213

🥰Excellent
Catalog No. T24055Cas No. 337972-47-1
Alias FAUC-213, FAUC213

FAUC 213 is a selective full antagonist of the dopamine D4 receptor.

FAUC 213

FAUC 213

🥰Excellent
Purity: 99.84%
Catalog No. T24055Alias FAUC-213, FAUC213Cas No. 337972-47-1
FAUC 213 is a selective full antagonist of the dopamine D4 receptor.
Pack SizePriceAvailabilityQuantity
2 mg31 €In Stock
5 mg53 €In Stock
10 mg84 €In Stock
25 mg170 €In Stock
50 mgInquiryIn Stock
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Purity:99.84%
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Product Introduction

Bioactivity
Description
FAUC 213 is a selective full antagonist of the dopamine D4 receptor.
Targets&IC50
D3 receptor (human):5.3 μM (Ki), D4.4 receptor (human):2.2 nM (Ki), D2 receptor (human):3.4 μM (Ki)
AliasFAUC-213, FAUC213
Chemical Properties
Molecular Weight326.82
FormulaC18H19ClN4
Cas No.337972-47-1
SmilesClc1ccc(cc1)N1CCN(Cc2cc3ccccn3n2)CC1
Relative Density.1.28g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 3.26 mg/mL (9.99 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0598 mL15.2989 mL30.5979 mL152.9894 mL
5 mM0.6120 mL3.0598 mL6.1196 mL30.5979 mL

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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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