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Slingshot inhibitor D3

🥰Excellent
Catalog No. T28804Cas No. 1715076-35-9
Alias JHN76359

Slingshot inhibitor D3 (JHN76359) is a potent inhibitor of the Protein Phosphatase Slingshot.

Slingshot inhibitor D3

Slingshot inhibitor D3

🥰Excellent
Purity: 99.53%
Catalog No. T28804Alias JHN76359Cas No. 1715076-35-9
Slingshot inhibitor D3 (JHN76359) is a potent inhibitor of the Protein Phosphatase Slingshot.
Pack SizePriceAvailabilityQuantity
1 mg$42In Stock
5 mg$98In Stock
10 mg$156In Stock
25 mg$313In Stock
50 mg$493In Stock
100 mg$745In Stock
1 mL x 10 mM (in DMSO)$98In Stock
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Purity:99.53%
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Product Introduction

Bioactivity
Description
Slingshot inhibitor D3 (JHN76359) is a potent inhibitor of the Protein Phosphatase Slingshot.
Targets&IC50
SSH:3 Μm(Slingshot 1 ), SSH:3.9 μM (Ki; Slingshot 2)
In vitro
Slingshot 1 had?IC50?value of 3 μM and Slingshot 2 had?Ki value of 3.9 μM.?Slingshot inhibitor D3 has similar inhibitory activitieswith Slingshot 1 and Slingshot 2.
In vivo
Slingshot inhibitor D3 (5 μM; 45 minutes; PC12 cells;) significantly blocks NGF-induced dephosphorylation of cofilin at 15 and 30 minutes. Slingshot inhibitor D3 (5 μM; 45 minutes; PC12 cells) significantly decreases the NGF-induced cell migration, consistent with its inhibitory role in cofilin dephosphorylation. Slingshot inhibitor D3 (HEK293 cells) specifically blocks angiotensin II-induced cofilin dephosphorylation. Slingshot inhibitor D3 prevents cofilin dephosphroylation through inhibition of Slingshot.
AliasJHN76359
Chemical Properties
Molecular Weight461.55
FormulaC25H19NO4S2
Cas No.1715076-35-9
SmilesCc1ccccc1N1C(=S)S\C(=C/c2ccc(OCc3ccc(cc3)C(O)=O)cc2)C1=O
Relative Density.1.44 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: 23.08 mg/mL (50 mM), Sonication and heating to 60℃ are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1666 mL10.8331 mL21.6661 mL108.3306 mL
5 mM0.4333 mL2.1666 mL4.3332 mL21.6661 mL
10 mM0.2167 mL1.0833 mL2.1666 mL10.8331 mL
20 mM0.1083 mL0.5417 mL1.0833 mL5.4165 mL
50 mM0.0433 mL0.2167 mL0.4333 mL2.1666 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
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