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VS-5584

🥰Excellent
Catalog No. T6103Cas No. 1246560-33-7
Alias VS5584, VS 5584, SB2343

VS-5584 (SB2343) is a pan-PI3K/mTOR kinase inhibitor.

VS-5584

VS-5584

🥰Excellent
Purity: 99.54%
Catalog No. T6103Alias VS5584, VS 5584, SB2343Cas No. 1246560-33-7
VS-5584 (SB2343) is a pan-PI3K/mTOR kinase inhibitor.
Pack SizePriceAvailabilityQuantity
5 mg$31In Stock
10 mg$56In Stock
25 mg$98In Stock
50 mg$139In Stock
100 mg$198In Stock
200 mg$297In Stock
1 mL x 10 mM (in DMSO)$35In Stock
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Purity:99.54%
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Product Introduction

Bioactivity
Description
VS-5584 (SB2343) is a pan-PI3K/mTOR kinase inhibitor.
Targets&IC50
PI3Kδ:2.7 nM, PI3Kβ:21 nM, PI3Kα:2.6 nM, PI3Kγ:3.0 nM, mTOR:3.4 nM
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)
AliasVS5584, VS 5584, SB2343
Chemical Properties
Molecular Weight354.41
FormulaC17H22N8O
Cas No.1246560-33-7
SmilesCC(C)n1c(C)nc2c(nc(nc12)N1CCOCC1)-c1cnc(N)nc1
Relative Density.1.48 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
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
Ethanol/DMSO
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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