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TG 100713

🥰Excellent
Catalog No. T6704Cas No. 925705-73-3
Alias TG100713

TG 100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.

TG 100713

TG 100713

🥰Excellent
Purity: 98.17%
Catalog No. T6704Alias TG100713Cas No. 925705-73-3
TG 100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.
Pack SizePriceAvailabilityQuantity
5 mg31 €In Stock
10 mg50 €In Stock
25 mg101 €In Stock
50 mg191 €In Stock
100 mg281 €In Stock
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Purity:98.17%
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Product Introduction

Bioactivity
Description
TG 100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.
Targets&IC50
PI3Kβ:215 nM, PI3Kδ:24 nM, PI3Kγ:50 nM, PI3Kα:165 nM
In vitro
TG 100713 also strongly inhibits EC proliferation. [1]
Kinase Assay
Kinase Assays: PI3K reactions are constructed by using recombinant human kinases, 3 μM ATP, phosphatidylinositol substrate, and cofactors, and reaction progression measured by using a luminescent-based detection system to quantify ATP consumption. Protein kinase assays are performed by using commercial screening services.
Cell Research
Human umbilical vein EC plated in 96-well cluster plates (5,000 cells/well) are cultured in assay medium (containing 0.5% serum and 50 ng/ml VEGF) in the presence or absence of test compounds (10 μM), and cell numbers are quantified by XTT assay.(Only for Reference)
AliasTG100713
Chemical Properties
Molecular Weight254.25
FormulaC12H10N6O
Cas No.925705-73-3
SmilesNc1nc(N)c2nc(cnc2n1)-c1cccc(O)c1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 2.5 mg/mL (10 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.9331 mL19.6657 mL39.3314 mL196.6568 mL
5 mM0.7866 mL3.9331 mL7.8663 mL39.3314 mL
10 mM0.3933 mL1.9666 mL3.9331 mL19.6657 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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