Product Data Sheet

JNK-1-IN-4

Catalog No. A40671

main product photo
JNK-1-IN-4 is a selective inhibitor of the c-Jun N-terminal kinase (JNK) family, targeting JNK-1, JNK-2, and JNK-3 with IC50 values of 2.7 nM, 19.0 nM, and 9.0 nM, respectively. This compound effectively inhibits the phosphorylation of c-Jun and decreases the expression of TGF-β1-induced epithelial-to-mesenchymal transition (EMT) marker proteins, including fibronectin and α-SMA. JNK-1-IN-4 demonstrates favorable pharmacokinetic properties, evidenced by a bioavailability of 69%, and has shown anti-fibrotic effects in bleomycin-induced models of idiopathic pulmonary fibrosis.
Chemical Information
Catalog NumA40671
M. Wt501.38
FormulaC22H25BrN6O3
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.3047795-60-5
Synonyms
SMILESCOC1=CC=C(NC2=NC(NC3=CC=C(OCCN(C)C)C=C3C(N)=O)=C(Br)C=N2)C=C1
Biological Activity
DescriptionJNK-1-IN-4 is a selective inhibitor of the c-Jun N-terminal kinase (JNK) family, targeting JNK-1, JNK-2, and JNK-3 with IC50 values of 2.7 nM, 19.0 nM, and 9.0 nM, respectively. This compound effectively inhibits the phosphorylation of c-Jun and decreases the expression of TGF-β1-induced epithelial-to-mesenchymal transition (EMT) marker proteins, including fibronectin and α-SMA. JNK-1-IN-4 demonstrates favorable pharmacokinetic properties, evidenced by a bioavailability of 69%, and has shown anti-fibrotic effects in bleomycin-induced models of idiopathic pulmonary fibrosis.
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