Molecule Details
InChIKeyVERWOWGGCGHDQE-UHFFFAOYSA-N
Compound NameCeritinib
Canonical SMILESCc1cc(Nc2ncc(Cl)c(Nc3ccccc3S(=O)(=O)C(C)C)n2)c(OC(C)C)cc1C1CCNCC1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)23
Pfam Stratification Cross-Family
Avg pChEMBL6.9
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB09063
Drug NameCeritinib
CAS Number1032900-25-6
Groups approved investigational
ATC Codes L01ED02
DescriptionCeritinib is used for the treatment of adults with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) following failure (secondary to resistance or intolerance) of prior crizotinib therapy. About 4% of patients with NSCLC have a chromosomal rearrangement that gen...

Categories: Anaplastic lymphoma kinase (ALK) inhibitors Antineoplastic Agents Antineoplastic and Immunomodulating Agents Bradycardia-Causing Agents Cytochrome P-450 CYP2C9 Inhibitors Cytochrome P-450 CYP2C9 Inhibitors (strength unknown) Cytochrome P-450 CYP3A Inhibitors Cytochrome P-450 CYP3A Substrates Cytochrome P-450 CYP3A4 Inhibitors Cytochrome P-450 CYP3A4 Inhibitors (weak) Cytochrome P-450 CYP3A4 Substrates Cytochrome P-450 CYP3A4 Substrates (strength unknown) Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index Cytochrome P-450 Enzyme Inhibitors Cytochrome P-450 Substrates Enzyme Inhibitors Hyperglycemia-Associated Agents Kinase Inhibitor Moderate Risk QTc-Prolonging Agents Narrow Therapeutic Index Drugs P-glycoprotein substrates P-glycoprotein substrates with a Narrow Therapeutic Index Protein Kinase Inhibitors QTc Prolonging Agents ROS1 tyrosine kinase inhibitors Receptor Protein-Tyrosine Kinases, antagonists & inhibitors Sulfur Compounds Tyrosine Kinase Inhibitors
Cross-references: BindingDB: 50436850 ChEBI: 78432 CHEMBL2403108 ChemSpider: 29315053 Drugs Product Database (DPD): 22568 D10551 PDB: 4MK PubChem:57379345 PubChem:310264998 RxCUI: 1535457 Wikipedia: Ceritinib ZINC: ZINC000096272772
Target Activities (23)
Target Gene Organism Category Pfam pChEMBL Type Source
P08922 ROS1 Homo sapiens Human PF00041 PF07714 8.7 IC50 ChEMBL;BindingDB
Q9UM73 ALK Homo sapiens Human PF12810 PF00629 PF07714 7.8 IC50 ChEMBL;BindingDB
Q9BXA7 TSSK1B Homo sapiens Human PF00069 7.6 IC50 ChEMBL;BindingDB
P06748 NPM1 Homo sapiens Human PF16276 PF03066 7.6 IC50 ChEMBL
Q13470 TNK1 Homo sapiens Human PF07714 PF22931 7.6 Kd ChEMBL
P00533 EGFR Homo sapiens Human PF00757 PF14843 PF07714 PF01030 PF21314 7.5 IC50 ChEMBL;BindingDB
P08069 IGF1R Homo sapiens Human PF00757 PF07714 PF01030 7.2 IC50 ChEMBL;BindingDB
P36888 FLT3 Homo sapiens Human PF00047 PF07714 7.1 IC50 ChEMBL;BindingDB
P06213 INSR Homo sapiens Human PF00757 PF17870 PF07714 PF01030 7.0 IC50 ChEMBL;BindingDB
Q9HC35 EML4 Homo sapiens Human PF23409 PF23414 PF03451 7.0 IC50 ChEMBL
Q07912 TNK2 Homo sapiens Human PF09027 PF11555 PF07714 PF22931 PF14604 6.8 IC50 ChEMBL
P04629 NTRK1 Homo sapiens Human PF13855 PF16920 PF07714 PF18613 6.7 IC50 BindingDB
P16591 FER Homo sapiens Human PF00611 PF07714 PF00017 6.7 Kd ChEMBL
Q05397 PTK2 Homo sapiens Human PF21477 PF00373 PF18038 PF03623 PF07714 6.7 Kd ChEMBL
P21802 FGFR2 Homo sapiens Human PF07679 PF13927 PF07714 6.6 IC50 ChEMBL
P08581 MET Homo sapiens Human PF07714 PF01437 PF01403 PF01833 6.6 IC50 ChEMBL;BindingDB
P07949 RET Homo sapiens Human PF00028 PF07714 PF17756 PF17812 PF17813 PF22540 6.4 IC50 ChEMBL;BindingDB
P22607 FGFR3 Homo sapiens Human PF21165 PF07679 PF13927 PF07714 6.4 IC50 ChEMBL
O60674 JAK2 Homo sapiens Human PF18379 PF18377 PF17887 PF07714 PF21990 6.2 IC50 ChEMBL;BindingDB
P06239 LCK Homo sapiens Human PF07714 PF00017 PF00018 6.2 IC50 ChEMBL
Q16566 CAMK4 Homo sapiens Human PF00069 6.2 Kd ChEMBL
P07948 LYN Homo sapiens Human PF07714 PF00017 PF00018 6.1 IC50 ChEMBL
P22455 FGFR4 Homo sapiens Human PF07679 PF13927 PF07714 6.0 IC50 ChEMBL
DrugBank Target Actions (5)
Target Gene Target Name Action Type
P08684 CYP3A4 Cytochrome P450 3A4 inhibitor enzymes
P11712 CYP2C9 Cytochrome P450 2C9 inhibitor enzymes
P08684 CYP3A4 Cytochrome P450 3A4 substrate enzymes
Q9UM73 ALK ALK tyrosine kinase receptor antagonist targets
P08183 ABCB1 ATP-dependent translocase ABCB1 substrate transporters