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Ponatinib is a kinase inhibitor used to treat patients with various types of chronic myeloid leukemia (CML). FDA approved on December 14, 2012.
- Mechanism
- Curator reviewed · 2 references
Ponatinib is a multi-target kinase inhibitor. Its primary cellular target is the Bcr-Abl tyrosine kinase protein which is constitutively active and promotes the progression of CML. This protein arises from the fused Bcr and Abl gene- what is commonly known as the Philadelphia chromosome. Ponatinib is unique in that it is especially useful in the treatment of resistant CML because it inhibits the tyrosine kinase activity of Abl and T315I mutant kinases. The T315I mutation confers resistance in cells as it prevents other Bcr-Abl inhibitors from binding to the Abl kinase. Other targets that ponatinib inhibits are members of the VEGFR, PDGFR, FGFR, EPH receptors and SRC families of kinases, and KIT, RET, TIE2, and FLT3. A decrease in tumour size expressing native or T315I mutant BCR-ABL have been observed in rats.
- Primary indication
- Ponatinib is indicated to treat adults with newly diagnosed Philadelphia chromosome positive acute lymphoblastic leukemia, in combination with chemotherapy.Curator reviewed · 9 structured indications
- Formula / weight
- C29H27F3N6O · 532.5595 g/mol (avg)
- First approval
- Canada, 2022 · United States, 2012 · European Union, 2021
- Code names
- AP-24534
- Brand names
- Iclusig
Resolves to
PHXJVRSECIGDHY-UHFFFAOYSA-NSMILESCN1CCN(CC2=CC=C(NC(=O)C3=CC(C#CC4=CN=C5C=CC=NN45)=C(C)C=C3)C=C2C(F)(F)F)CC1What you can answer from here — as of September 12, 2026
Which drugs share a target with Ponatinib, and which of those have an active Phase 3 trial?