HG-14-10-04 is a potent and specific ALK inhibitor with IC50 of 20 nM.

Brigatinib is a selective ALK inhibitor with IC50 value of 0.37nM, and also inhibits ROS1, FLT3, FLT3-D835Y mutant and EGFR less potently.

AP26113 is an analog of AP26113 which is a potent and selective ALK inhibitor. It is also an inhibitor of EGFR.

JH-VIII-157-02 is a structural analogue of alectinib, acts as an ALK inhibitor, and shows an IC50 of 2 nM for echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) G1202R in cells.

ALK inhibitor 2 is a selective inhibitor for the ALK kinase.

NVP-TAE684 is a potent and selective ALK inhibitor with IC50 of 3 nM in a cell-free assay, 100-fold more sensitive for ALK than InsR.

6-Demethoxytangeretin is a natural product isolated and purified from the herbs of Andrographis paniculata with anti-inflammatory activity.

Trigonelline HCl is an alkaloid with potential antidiabetic activity, is present in considerable amounts in coffee.

Ensartinib is a potent inhibitor ofALK, which is used to treat non-small-cell lung cancer.

BLU-782 is a potent, selective ALK2 inhibitor that prevents edema and heterotopic bone formation in a FOP mouse model.