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PI3K/AKT-IN-1

🥰Excellent
Catalog No. T62997Cas No. 3033069-84-7

PI3K/AKT-IN-1 is a dual PI3K and AKT inhibitor with anti-cancer activity. It inhibits PI3Kγ, PI3Kδ, and AKT, suppressing the PI3K/AKT pathway and inducing caspase 3-dependent apoptosis, suitable for cancer research.

PI3K/AKT-IN-1

PI3K/AKT-IN-1

🥰Excellent
Catalog No. T62997Cas No. 3033069-84-7
PI3K/AKT-IN-1 is a dual PI3K and AKT inhibitor with anti-cancer activity. It inhibits PI3Kγ, PI3Kδ, and AKT, suppressing the PI3K/AKT pathway and inducing caspase 3-dependent apoptosis, suitable for cancer research.
Pack SizePriceAvailabilityQuantity
1 mg$71In Stock
5 mg$172In Stock
10 mg$242In Stock
25 mg$416In Stock
50 mg$565In Stock
100 mg$826In Stock
1 mL x 10 mM (in DMSO)$167In Stock
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Product Introduction

Bioactivity
Description
PI3K/AKT-IN-1 is a dual PI3K and AKT inhibitor with anti-cancer activity. It inhibits PI3Kγ, PI3Kδ, and AKT, suppressing the PI3K/AKT pathway and inducing caspase 3-dependent apoptosis, suitable for cancer research.
Targets&IC50
PI3Kγ:6.99 μM, PI3Kδ:4.01 μM, Akt:3.36 μM
In vitro
PI3K/AKT-IN-1 showed excellent cytotoxic activity in breast cancer MCF-7 and leukemia K562 cell lines with IC50 values of 3.22 μM and 2.62 μM, respectively.
PI3K/AKT-IN-1 causes the cell cycle to stall in the S phase, leading to apoptosis induced by caspase 3 activation of leukemia (k562) cells. [1]
In vivo
The median lethal dose (LD50) of PI3K/AKT-IN-1 was greater than the test dose of 2000 mg/kg, indicating that PI3K/ AKt-in-1 was non-toxic and well tolerated by experimental animals. [1]
Chemical Properties
Molecular Weight465.53
FormulaC23H23N5O4S
Cas No.3033069-84-7
SmilesN#CC=1C(=NC(=NC1C=2C=CC(OC)=CC2)SC)NN=CC3=CC(OC)=C(OC)C(OC)=C3
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: 40 mg/mL (85.92 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1481 mL10.7404 mL21.4809 mL107.4045 mL
5 mM0.4296 mL2.1481 mL4.2962 mL21.4809 mL
10 mM0.2148 mL1.0740 mL2.1481 mL10.7404 mL
20 mM0.1074 mL0.5370 mL1.0740 mL5.3702 mL
50 mM0.0430 mL0.2148 mL0.4296 mL2.1481 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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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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