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CC-401 (hydrochloride)

CC-401 hydrochloride is a potent inhibitor of all three forms of JNK with Ki of 25 to 50 nM.

Product Specifications

CAS Number

[1438391-30-0]

Product Name Alternative

CC401 HCl

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

JNK

Type

Reference compound

Related Pathways

MAPK/ERK Pathway

Applications

Cancer-Kinase/protease

Field of Research

Cancer

Assay Protocol

https://www.medchemexpress.com/CC-401-hydrochloride.html

Purity

99.35

Solubility

DMSO : 100 mg/mL (ultrasonic) |H2O : 12.5 mg/mL (ultrasonic)

Smiles

C1(C2=CC=CC(OCCN3CCCCC3)=C2)=NNC4=C1C=C(C=C4)C5=NC=NN5.Cl

Molecular Formula

C22H25ClN6O

Molecular Weight

424.93

Precautions

H302, H315, H319, H335

References & Citations

[1]Ma FY, et al. A pathogenic role for c-Jun amino-terminal kinase signaling in renal fibrosis and tubular cell apoptosis. J Am Soc Nephrol. 2007 Feb;18 (2) :472-84.|[2]Vasilevskaya IA, et al. Inhibition of JNK Sensitizes Hypoxic Colon Cancer Cells to DNA-Damaging Agents. Clin Cancer Res. 2015 Sep 15;21 (18) :4143-52.|[3]Ma FY, et al. Blockade of the c-Jun amino terminal kinase prevents crescent formation and halts established anti-GBM glomerulonephritis in the rat. Lab Invest. 2009 Apr;89 (4) :470-84.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, sealed storage, away from moisture)

Scientific Category

Reference compound1

Clinical Information

Phase 1

Isoform

JNK

Citation 01

Harvard Medical School LINCS LIBRARY|Int Immunopharmacol. 2024 Dec 9:145:113781.|Science. 2017 Dec 1;358 (6367) :eaan4368.|Cell Syst. 2018 Apr 25;6 (4) :424-443.e7.|J Med Chem. 2023 Mar 23;66 (6) :4106-4130.|Mol Cancer Res. 2016 Aug;14 (8) :753-63.

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