CC 401 dihydrochloride
Tocris Bioscience, part of Bio-Techne | Catalog # 6258
High affinity JNK inhibitor; also inhibits HCMV replication
Key Product Details
Description
High affinity JNK inhibitor; also inhibits HCMV replication
Product Description
CC 401 dihydrochloride is a high affinity JNK inhibitor (Ki values are 25-50 nM). Inhibits JNK via competitive binding of the ATP-binding site of active, phosphorylated JNK. Exhibits > 40-fold selectivity for JNK over p38, ERK, IKK2, protein kinase C, Lck and ZAP70. Hepatoprotective. Also inhibits HCMV replication.Product Specifications
Molecular Weight
461.39
Formula
C22H24N6O.2HCl
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
3-[3-[2-(1-Piperidinyl)ethoxy]phenyl]-5-(1H-1,2,4-triazol-5-yl)-1H-indazole dihydrochloride
CAS Number
2250025-96-6
PubChem ID
66576998
InChI Key
LDUPODIOUWRGCQ-UHFFFAOYSA-N
SMILES
N1(CCCCC1)CCOC2=CC=CC(C3=NNC4=CC=C(C5=NN=CN5)C=C34)=C2.Cl.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 46.14 | 100 | |
| DMSO | 46.14 | 100 |
Preparing Stock Solutions
for CC 401 dihydrochloride
The following data is based on the product molecular weight 461.39
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.17 mL | 10.84 mL | 21.67 mL |
| 5 mM | 0.43 mL | 2.17 mL | 4.33 mL |
| 10 mM | 0.22 mL | 1.08 mL | 2.17 mL |
| 50 mM | 0.04 mL | 0.22 mL | 0.43 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Vasilevskaya Inhibition of JNK sensitizes hypoxic colon cancer cells to DNA-damaging agents. Clin.Cancer.Res. 2015 PMID: 26023085
- Zhang The c-Jun N-terminal kinase inhibitor SP600125 inhibits human cytomegalovirus replication. J.Med.Virol. 2015 PMID: 26058558
- Ma Blockade of the c-Jun amino terminal kinase prevents crescent formation and halts established anti-GBM glomerulonephritis in the rat. Lab.Invest. 2009 PMID: 19188913
- Ma A pathogenic role for c-Jun amino-terminal kinase signaling in renal fibrosis and tubular cell apoptosis. J.Am.Soc.Nephrol. 2007 PMID: 17202416
- Uehara JNK mediates hepatic ischemia reperfusion injury. J.Hepatol. 2005 PMID: 15885356
- Uehara c-Jun N-terminal kinase mediates hepatic injury after rat liver transplantation. Transplantation. 2004 PMID: 15316358
Product Specific Notices for CC 401 dihydrochloride
For research use only
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