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VS-5584

VS-5584
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Purity:98.41%
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VS-5584

Catalog No. T6103Cas No. 1246560-33-7
VS-5584 (SB2343) is a pan-PI3K/mTOR kinase inhibitor.
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
1 mg$34In Stock
2 mg$48In Stock
5 mg$77In Stock
10 mg$101In Stock
25 mg$181In Stock
50 mg$328In Stock
100 mg$531In Stock
1 mL x 10 mM (in DMSO)$84In Stock
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Product Introduction

Bioactivity
Description
VS-5584 (SB2343) is a pan-PI3K/mTOR kinase inhibitor.
In vitro
VS-5584 is an ATP-competitive inhibitor which selectively inhibits PI3K/mTOR signaling with equivalent low nanomolar potency against all human Class I PI3K isoforms and mTOR kinase. VS-5584 is approximately 10-fold selective for cancer stem cells with an EC50 of 15 nM in HMLE breast cancer cells. VS-5584 preferentially decreases CD44Hi/CD24Lo cells in an HMLER immortalized mammary cancer cell line. In SUM159 cells, VS-5584 effectively eliminates the cancer stem cell side population. [1] A large human cancer cell line panel screen (436 lines) reveals broad antiproliferative sensitivity and that cells harboring mutations in PI3KCA are generally more sensitive toward VS-5584 treatment. In the FLT3-ITD harboring MV4-11 cells, VS-5584 blocks pAkt (S473) and pAkt (T308) with IC50 of 12 and 13 nM, respectively. The IC50 of VS-5584 for pS6 (S240/244), pAkt (S473), and pAkt (T308) are 20, 23, and 15 nM, respectively. [2]
In vivo
In mice bearing triple negative breast cancer tumors, oral dosing of VS-5584 decreases tumor cancer stem cells and induces tumor regression in taxane-resistant models. [1] In a PTENnull human prostate PC3 xenograft model, treatment with VS-5584 leads to significant tumor growth inhibition (TGI) of 79% and 113% for 11 and 25 mg/kg, respectively. In a FLT3-ITD AML xenograft model, VS-5584 treatment induces dose-dependent inhibition of tumor growth (28% for 3.7 mg/kg and 76% for 11 mg/kg). [2]
Kinase Assay
In vitro mTOR kinase assays : The reaction mixture consisted of the following components in 10 μL assay buffer (50 mM Hepes pH 7.5, 10 mM MgCl 2, 3 mM MnCl 2, 1 mM EGTA, 2 mM DTT, 0.01%Tween-20): 0.10 μg/mL of in-house generated mTOR enzyme, 0.05 μM ULight-eIF4E-binding protein 1 (Thr37/46) peptide and 10 μM ATP. The mixture is incubated for 60 min at room temperature. 10 μL of Detection mixture consisted of 16 mM EDTA, 0.004 mM Eu-W1024-labeled Anti-Phospho-eIF4E-binding protein 1-(Thr37/46) antibody and 1X LANCE? Detection Buffer is then added and incubated for 60 min.
Cell Research
CellTiter-Glo assay(Only for Reference)
AliasSB2343, VS 5584, VS5584
Chemical Properties
Molecular Weight354.41
FormulaC17H22N8O
Cas No.1246560-33-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
Ethanol: 3 mg/mL (8.46 mM)
DMSO: 66 mg/mL (186.2 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO/Ethanol
1mg5mg10mg50mg
1 mM2.8216 mL14.1080 mL28.2159 mL141.0795 mL
5 mM0.5643 mL2.8216 mL5.6432 mL28.2159 mL
DMSO
1mg5mg10mg50mg
10 mM0.2822 mL1.4108 mL2.8216 mL14.1080 mL
20 mM0.1411 mL0.7054 mL1.4108 mL7.0540 mL
50 mM0.0564 mL0.2822 mL0.5643 mL2.8216 mL
100 mM0.0282 mL0.1411 mL0.2822 mL1.4108 mL

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