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AMG 579

Catalog No. T14217Cas No. 1227067-61-9
Alias AMG-579

AMG 579 is an efficacious and selective inhibitor of PDE10A (IC50 = 0.1 nM).

AMG 579

AMG 579

Purity: 99.35%
Catalog No. T14217Alias AMG-579Cas No. 1227067-61-9
AMG 579 is an efficacious and selective inhibitor of PDE10A (IC50 = 0.1 nM).
Pack SizePriceAvailabilityQuantity
1 mg$30In Stock
2 mg$39In Stock
5 mg$67In Stock
10 mg$107In Stock
25 mgInquiryIn Stock
50 mgInquiryIn Stock
1 mL x 10 mM (in DMSO)$75In Stock
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Purity:99.35%
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Product Introduction

Bioactivity
Description
AMG 579 is an efficacious and selective inhibitor of PDE10A (IC50 = 0.1 nM).
Targets&IC50
PDE10A:0.1 nM
In vivo
AMG 579 statistically reduces PCP-induced behavior in rats within 2 hours. In the PCP-LMA model, the minimum effective dose of AMG 579 was 0.3 mg/kg. AMG 579 has an excellent oral bioavailability of 72% in dogs[1].
AliasAMG-579
Chemical Properties
Molecular Weight441.48
FormulaC25H23N5O3
Cas No.1227067-61-9
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 37.8 mg/mL (85.6 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2651 mL11.3255 mL22.6511 mL113.2554 mL
5 mM0.4530 mL2.2651 mL4.5302 mL22.6511 mL
10 mM0.2265 mL1.1326 mL2.2651 mL11.3255 mL
20 mM0.1133 mL0.5663 mL1.1326 mL5.6628 mL
50 mM0.0453 mL0.2265 mL0.4530 mL2.2651 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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