Description
An inhibitor of the Dvl PDZ domain (Kd = 240 μM for mouse Dvl1 PDZ domain); reduces expression of the Wnt target gene, Siamois, in Xenopus embryos and inhibits the ability of injected Wnt3A to induce formation of a secondary axis (180 ng); inhibits proliferation of NIH/3T3 fibroblasts, restrains their migration in a scratch assay, and blocks the accelerating effect of TGF-β on fibroblast migration (>10 μM); reduces the severity of bleomycin-induced pulmonary fibrosis and expression of α-SMA collagen I, TGF-β, and β-catenin in lung in mice (5 mg/kg per day for 14 days)
Formal name: N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl-(2S)-2-hydroxy-3-methylbutanoyl-L-alanine, (1S)-1-carboxy-2-methylpropyl ester
Synonyms:
Molecular weight: 460.5
CAS: 144678-63-7
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Small Molecule Inhibitors||Research Area|Cell Biology|Cell Signaling|Wnt Signaling||Research Area|Immunology & Inflammation