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JX06 PDK inhibitor

Cat.No.S0983

JX06 is a selective covalent inhibitor of PDK1 in cells. This compound dose-dependently inhibits PDK1, PDK2 and PDK3 with IC50 0.049 μM, 0.101 μM and 0.313 μM, respectively.
JX06 PDK inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 324.51

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Quality Control

Batch: S098301 DMSO]65 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 99.99%
99.99

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
Kelly Antiproliferative assay 72 hrs Antiproliferative activity against human Kelly cells after 72 hrs by CCK8 assay, IC50=0.289μM. 28230989
A549 Antiproliferative assay 72 hrs Antiproliferative activity against human A549 cells after 72 hrs by CCK8 assay, IC50=0.48μM. 28230989
A549 Antitumor activity assay 40 to 80 mg/kg 21 days Antitumor activity against human A549 cells xenografted in BALB/c nude mouse assessed as reduction in tumor weight at 40 to 80 mg/kg, ip for 21 days measured on day 21 post dose 28230989
Click to View More Cell Line Experimental Data

Solubility

In vitro
Batch:

DMSO : 65 mg/mL (200.3 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg
g
μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
% DMSO
+
%

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Chemical Information, Storage & Stability

Molecular Weight 324.51 Formula

C10H16N2O2S4

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 729-46-4 -- Storage of Stock Solutions

Synonyms N/A Smiles C1COCCN1C(=S)SSC(=S)N2CCOCC2

Mechanism of Action

Targets/IC50/Ki
PDK1
(Cell-free assay)
0.049 μM
PDK2
(Cell-free assay)
0.101 μM
PDK3
(Cell-free assay)
0.313 μM
References

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