Molecule Details
InChIKeyXXJWYDDUDKYVKI-UHFFFAOYSA-N
Compound NameCediranib
Canonical SMILESCOc1cc2c(Oc3ccc4[nH]c(C)cc4c3F)ncnc2cc1OCCCN1CCCC1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)52
Pfam Stratification Cross-Family
Avg pChEMBL7.0
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB04849
Drug NameCediranib
CAS Number288383-20-0
Groups investigational
ATC Codes L01EK02
DescriptionThe novel indole-ether quinazoline Cediranib is a highly potent (IC<sub>50</sub> &lt; 1 nmol/L) ATP-competitive inhibitor of recombinant KDR tyrosine kinase in vitro. It is being developed clinically as a once-daily oral therapy for the treatment of cancer.

Categories: Antineoplastic Agents Antineoplastic and Immunomodulating Agents Enzyme Inhibitors Heterocyclic Compounds, Fused-Ring Protein Kinase Inhibitors Tyrosine Kinase Inhibitors Vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors
Cross-references: BindingDB: 50331096 ChEBI: 94782 CHEMBL491473 ChemSpider: 8109103 PubChem:9933475 PubChem:175426860 Wikipedia: AZD2171 ZINC: ZINC000003948085
Target Activities (52)
Target Gene Organism Category Pfam pChEMBL Type Source
P10721 KIT Homo sapiens Human PF00047 PF07714 9.3 Kd ChEMBL;BindingDB
P35968 KDR Homo sapiens Human PF07679 PF00047 PF13895 PF22971 PF07714 PF21339 PF17988 PF22854 9.0 IC50 ChEMBL;BindingDB
Q08345 DDR1 Homo sapiens Human PF21114 PF00754 PF07714 8.8 Kd ChEMBL;BindingDB
P35916 FLT4 Homo sapiens Human PF07679 PF13927 PF22971 PF07714 PF21339 PF17988 PF22854 8.4 IC50 ChEMBL;BindingDB
P09619 PDGFRB Homo sapiens Human PF00047 PF13927 PF25305 PF07714 8.3 Kd ChEMBL;BindingDB
P17948 FLT1 Homo sapiens Human PF07679 PF00047 PF13927 PF22971 PF07714 PF21339 PF17988 PF22854 8.3 IC50 ChEMBL;BindingDB
Q8TDR2 STK35 Homo sapiens Human PF00069 8.3 Kd ChEMBL;BindingDB
P07949 RET Homo sapiens Human PF00028 PF07714 PF17756 PF17812 PF17813 PF22540 8.1 Kd ChEMBL;BindingDB
Q9ULC5 ACSL5 Homo sapiens Human PF00501 8.1 Kd ChEMBL
P16234 PDGFRA Homo sapiens Human PF07679 PF25305 PF07714 8.0 IC50 ChEMBL;BindingDB
P07333 CSF1R Homo sapiens Human PF00047 PF25305 PF07714 7.9 Kd ChEMBL;BindingDB
Q9H2G2 SLK Homo sapiens Human PF00069 PF12474 7.7 Kd ChEMBL;BindingDB
O94804 STK10 Homo sapiens Human PF00069 PF12474 7.6 Kd ChEMBL;BindingDB
P22607 FGFR3 Homo sapiens Human PF21165 PF07679 PF13927 PF07714 7.6 Kd ChEMBL;BindingDB
P21802 FGFR2 Homo sapiens Human PF07679 PF13927 PF07714 7.5 Kd ChEMBL;BindingDB
Q9UF33 EPHA6 Homo sapiens Human PF14575 PF25599 PF01404 PF07699 PF00041 PF07714 PF00536 7.4 Kd ChEMBL;BindingDB
P11362 FGFR1 Homo sapiens Human PF07679 PF00047 PF07714 7.4 Kd ChEMBL;BindingDB
Q16832 DDR2 Homo sapiens Human PF21114 PF00754 PF07714 7.3 Kd ChEMBL;BindingDB
P06239 LCK Homo sapiens Human PF07714 PF00017 PF00018 7.2 Kd ChEMBL;BindingDB
P00519 ABL1 Homo sapiens Human PF08919 PF07714 PF00017 PF00018 7.1 Kd ChEMBL;BindingDB
P12931 SRC Homo sapiens Human PF07714 PF00017 PF00018 7.1 Kd ChEMBL;BindingDB
O43353 RIPK2 Homo sapiens Human PF00619 PF07714 7.0 Kd ChEMBL;BindingDB
Q9Y4K4 MAP4K5 Homo sapiens Human PF00780 PF00069 7.0 Kd ChEMBL;BindingDB
P51451 BLK Homo sapiens Human PF07714 PF00017 PF00018 6.9 Kd ChEMBL;BindingDB
Q02763 TEK Homo sapiens Human PF00041 PF10430 PF07714 6.8 Kd ChEMBL;BindingDB
P21860 ERBB3 Homo sapiens Human PF00757 PF14843 PF07714 PF01030 6.7 Kd ChEMBL;BindingDB
O15197 EPHB6 Homo sapiens Human PF14575 PF25599 PF01404 PF07699 PF00041 PF07714 PF07647 6.7 Kd ChEMBL;BindingDB
P00533 EGFR Homo sapiens Human PF00757 PF14843 PF07714 PF01030 PF21314 6.6 Kd ChEMBL;BindingDB
Q56UN5 MAP3K19 Homo sapiens Human PF00069 6.6 Kd ChEMBL;BindingDB
P07947 YES1 Homo sapiens Human PF07714 PF00017 PF00018 6.6 Kd ChEMBL;BindingDB
P07948 LYN Homo sapiens Human PF07714 PF00017 PF00018 6.6 Kd ChEMBL;BindingDB
P35590 TIE1 Homo sapiens Human PF00041 PF00047 PF07714 6.5 Kd ChEMBL;BindingDB
P04626 ERBB2 Homo sapiens Human PF00757 PF14843 PF07714 PF01030 PF21314 6.4 Ki ChEMBL
P30530 AXL Homo sapiens Human PF00041 PF13927 PF07714 6.3 Kd ChEMBL;BindingDB
P06241 FYN Homo sapiens Human PF07714 PF00017 PF00018 6.3 Ki ChEMBL
O75460 ERN1 Homo sapiens Human PF00069 PF06479 6.3 Kd ChEMBL;BindingDB
Q12851 MAP4K2 Homo sapiens Human PF00780 PF00069 6.3 Kd ChEMBL;BindingDB
Q8N4C8 MINK1 Homo sapiens Human PF00780 PF00069 6.3 Kd ChEMBL;BindingDB
Q9BYT3 STK33 Homo sapiens Human PF00069 6.3 Kd ChEMBL;BindingDB
P08581 MET Homo sapiens Human PF07714 PF01437 PF01403 PF01833 6.2 Kd ChEMBL;BindingDB
Q13882 PTK6 Homo sapiens Human PF07714 PF00017 PF00018 6.2 Kd ChEMBL;BindingDB
P08631 HCK Homo sapiens Human PF07714 PF00017 PF00018 6.2 Kd ChEMBL;BindingDB
Q15375 EPHA7 Homo sapiens Human PF14575 PF25599 PF01404 PF07699 PF00041 PF07714 PF00536 6.2 Kd ChEMBL
P42684 ABL2 Homo sapiens Human PF08919 PF07714 PF00017 PF00018 6.1 Kd ChEMBL;BindingDB
P42685 FRK Homo sapiens Human PF07714 PF00017 PF00018 6.1 Kd ChEMBL;BindingDB
Q9UKE5 TNIK Homo sapiens Human PF00780 PF00069 6.1 Kd ChEMBL;BindingDB
Q06418 TYRO3 Homo sapiens Human PF00041 PF07679 PF07714 6.1 Kd ChEMBL;BindingDB
P22455 FGFR4 Homo sapiens Human PF07679 PF13927 PF07714 6.1 Kd ChEMBL;BindingDB
Q92918 MAP4K1 Homo sapiens Human PF00780 PF00069 6.0 Kd ChEMBL;BindingDB
P16591 FER Homo sapiens Human PF00611 PF07714 PF00017 6.0 Ki ChEMBL
P29376 LTK Homo sapiens Human PF12810 PF07714 6.0 Ki ChEMBL
Q04912 MST1R Homo sapiens Human PF07714 PF01437 PF01403 PF01833 6.0 Ki ChEMBL
DrugBank Target Actions (1)
Target Gene Target Name Action Type
P35968 KDR Vascular endothelial growth factor receptor 2 inhibitor targets