As a way to rationalise the noticed ABL kinase inhibitory success from the 3D structural point of view, the direct compounds I and II, plus the newly designed derivatives 4a, 4b, and five ended up docked from the catalytic kinase domains of BCR-ABLWT (PDB code: 3OXZ) and BCR-ABLT315I (PDB code: https://paxtonvphxm.blogs100.com/31538892/details-fiction-and-indazole-tautomers