JNK-IN-8

This product is for research use only, not for human use. We do not sell to patients.

JNK-IN-8
For small sizes, please check our retail website as below: www.invivochem.com
Size Price Stock
250mg$1050Check With Us
500mg$1650Check With Us
1g$2475Check With Us

Cat #: V0472 CAS #: 1410880-22-6 Purity ≥ 98%

Description: JNK-IN-8 (JNK Inhibitor XVI; JNK-IN8) is the first irreversible/covalent inhibitor of pan-JNK (c-Jun N-terminal Kinase) with potential antitumor activity.

References: Bengoa-Vergniory N, et al. A switch from canonical to noncanonical Wnt signaling mediates early differentiation of human neural stem cells. Stem Cells. 2014 Dec;32(12):3196-208. 

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Molecular Weight (MW)507.59
Molecular FormulaC29H29N7O2
CAS No.1410880-22-6
Storage-20℃ for 3 years in powder formr
-80℃ for 2 years in solvent
Solubility In VitroDMSO: 100 mg/mL (197.0 mM)r
Water: <1 mg/mLr
Ethanol:<1 mg/mL
Solubility In Vivo2% DMSO+30% PEG 300+5% Tween 80+ddH2O: 10mg/mL
SMILES CodeCN(C/C=C/C(NC1=CC=CC(C(NC2=CC=C(C(C)=C2)NC3=NC=CC(C4=CN=CC=C4)=N3)=O)=C1)=O)C
SynonymsSynonym: JNK Inhibitor XVI; JNK-IN 8; JNK-IN8; JNK-IN 8; c-Jun N-terminal Kinase Inhibitor XVI.
ProtocolIn VitroJNK-IN-8 (GMP) (2 μM, 7 days) enhances the self-renewal of human hematopoietic stem cells (HSCs) through the downregulation of C-JUN phosphorylation. JNK-IN-8 (GMP) (10 μM) reduces WNT3A-mediated neuronal differentiation.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Preparing Stock Solutions
Solvent volume to be added Mass (the weight of a compound)
Mother liquor concentration 1mg5mg10mg20mg
1mM1.9701 mL9.8505 mL19.7009 mL39.4019 mL
5mM0.3940 mL1.9701 mL3.9402 mL7.8804 mL
10mM0.1970 mL0.9850 mL1.9701 mL3.9402 mL
20mM0.0985 mL0.4925 mL0.9850 mL1.9701 mL
Quality Control Documentation
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start) × Volume(start) = Concentration(final) × Volume(final)

This equation is commonly abbreviated as: C1 V1 = C2 V2

Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg Average weight of animals g Dosing volume per animal µL Number of animals
Step Two: Enter the in vivo formulation
%DMSO + % + %Tween 80 + %ddH2O

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 add µL PEG300, mix and clarify, next add µL Tween 80,mix and clarify, next add µL ddH2O,mix and clarify.
Note:
  • (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
  • (2) Be sure to add the solvent(s) in order.