Click Here for 5% Off Your First Aladdin Purchase!

TCS JNK 6o - ≥98%(HPLC), high purity , CAS No.894804-07-0, Inhibitor of mitogen-activated protein kinase 10;Inhibitor of mitogen-activated protein kinase 8;Inhibitor of mitogen-activated protein kinase 9

  • Moligand™
  • ≥98%(HPLC)
Item Number
T288865
Grouped product items
SKUSizeAvailabilityPrice Qty
T288865-5mg
5mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$147.90
T288865-10mg
10mg
In stock
$246.90
T288865-25mg
25mg
In stock
$555.90
T288865-50mg
50mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,000.90
T288865-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,800.90

Selective JNK inhibitor

Basic Description

SynonymsJNK Inhibitor VIII|894804-07-0|TCS JNK 6o|N-(4-Amino-5-cyano-6-ethoxypyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamide|aminopyridine deriv. 2|TCS JNK 6o(JNK Inhibitor VIII)|N-(4-Amino-5-cyano-6-ethoxy-2-pyridinyl)-2,5-dimethoxybenzeneacetamide|Kinome_3020|JN
Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsCell permeable: yes Target Ki: 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively Product competes with ATP. Reversible: yes
Storage TempProtected from light,Store at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of mitogen-activated protein kinase 10;Inhibitor of mitogen-activated protein kinase 8;Inhibitor of mitogen-activated protein kinase 9
Product Description

Product Description
A cell-permeable pyridinylamide compound that acts as an ATP-competitive, reversible inhibitor of JNK (Ki = 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively) and displays excellent selectivity over 72 other kinases. Inhibits c-jun phosphorylation with an EC50 of 920 nM in HepG2 cells. Preferentially blocks the growth of PTEN null mouse embryonic fibroblasts.

Names and Identifiers

IUPAC Name N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamide
INCHI InChI=1S/C18H20N4O4/c1-4-26-18-13(10-19)14(20)9-16(22-18)21-17(23)8-11-7-12(24-2)5-6-15(11)25-3/h5-7,9H,4,8H2,1-3H3,(H3,20,21,22,23)
InChi Key KQMPRSZTUSSXND-UHFFFAOYSA-N
Canonical SMILES CCOC1=C(C(=CC(=N1)NC(=O)CC2=C(C=CC(=C2)OC)OC)N)C#N
Isomeric SMILES CCOC1=C(C(=CC(=N1)NC(=O)CC2=C(C=CC(=C2)OC)OC)N)C#N
PubChem CID 11624601
Molecular Weight 356.38

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

5 results found

Lot NumberCertificate TypeDateItem
F2204949Certificate of AnalysisMar 07, 2022 T288865
F2204950Certificate of AnalysisMar 07, 2022 T288865
F2204951Certificate of AnalysisMar 07, 2022 T288865
F2204952Certificate of AnalysisMar 07, 2022 T288865
F2204953Certificate of AnalysisMar 07, 2022 T288865

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 35.64, Max Conc. mM: 100
Sensitivitylight sensitive

Related Documents

References

1. Szczepankiewicz BG, Kosogof C, Nelson LT, Liu G, Liu B, Zhao H, Serby MD, Xin Z, Liu M, Gum RJ et al..  (2006)  Aminopyridine-based c-Jun N-terminal kinase inhibitors with cellular activity and minimal cross-kinase activity..  J Med Chem,  49  (12): (3563-80).  [PMID:16759099]

Solution Calculators