Crizotinib

ALK Inhibitor
DB08865
Approved Indication

Crizotinib is used for the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) that is anaplastic-lymphoma kinase (ALK)-positive as detected by a FDA-approved test.

2 Targets
50 Resistance Mutations
134 References
2XP2 Structure Loaded
3D Structure PDB: 2XP2
Switch structure: RCSB ↗
Mechanism of Action

Crizotinib is a tyrosine kinase receptor inhibitor. More specifically, it inhibits anaplastic lymphoma kinase (ALK), hepatocyte growth factor receptor (HGFR, c-MET), and Recepteur d'Origine Nantais (RON). Abnormalities in the ALK gene caused by mutations or translocations may lead to expression of oncogenic fusion proteins. In patients with NSCLC, they have the EML4-ALK gene. Crizotinib inhibits ALK tyrosine kinase which ultimately results in decreased proliferation of cells that carry the genetic mutation and tumour survivability.

Resistance Mutations — 158 resistance samples observed in COSMIC
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ALK
p.C1156F 5 p.C1156Y 5 p.C779Y p.C88Y p.E1210K 5 p.F106L p.F106V p.F1174C 5 p.F1174L 5 p.F1174V 5 p.F797L p.F797V p.G1128A 5 p.G1202R 5 p.G1269A 5 p.G134R p.G201A p.G60A p.G751A p.G825R p.G892A p.I103T p.I1171T 5 p.I794T p.L1152R 5 p.L1196M 5 p.L128M p.L819M p.S1206F 5 p.S1206Y 5 p.S138Y p.S829Y p.T1151M 5 p.T1151R 5 p.T1151dup p.T774dup p.T83dup
KIT
p.D816G 5
KRAS
p.G12V 5
MET
p.D1228N 5 p.D1246H 5 p.D1246N 5 p.D1249Y p.G1181R 2 p.Y1230C 5 p.Y1230H 5 p.Y1248C 5 p.Y1248H 5 p.Y1248S
ROS1
p.G2032R 5

Resistance mutations sourced from COSMIC Drug Resistance database. Cyan = on-target · Amber = off-target · numbered badge = PubMed references for that mutation

Details
DrugBank ID DB08865 ↗
Approval Date 2011-08-26
Molecular Weight 450.337 g/mol
Drug Class ALK Inhibitor
ATC Codes L01XE16
Synonyms (R)-crizotinib, Crizotinib, Crizotinibum
SMILES
C[C@@H](OC1=CC(=CN=C1N)C1=CN(N=C1)C1CCNCC1)C1=C(Cl)C=CC(F)=C1Cl
ADMET Profile
Computing properties…
Drug References (DrugBank)