SMU-B is the orally active inhibitor for ALK ( IC 50 <0.5 nM), c-ros oncogene 1 (ROS1), c-MET ( IC 50 =1.87 nM) and AXL ( IC 50 =28.9 nM). SMU-B inhibits the proliferation of MKN45, H1993 and H441 with IC 50 s of 0.02 μM, 1.58 μM and 2.82 μM, respectively. SMU-B exhibits antitumor efficacy in mouse models.
Products | Products > Disease Areas > Cancer | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Signaling Pathways > ROS Kinase | Products > Signaling Pathways > Anaplastic lymphoma kinase (ALK) | Products > Signaling Pathways > TAM Receptor | Products > Signaling Pathways > c-Met/HGFR
Please leave a message for us or use the following ways to contact us, we will reply to you as soon as possible, and provide you with the most sincere service, thank you.