Sunitinib

EGFR Inhibitor
DB01268
Approved Indication

For the treatment of advanced renal cell carcinoma as well as the treatment of gastrointestinal stromal tumor after disease progression on or intolerance to imatinib mesylate.

8 Targets
6 Resistance Mutations
12 References
4AGD Structure Loaded
3D Structure PDB: 4AGD
Switch structure: RCSB ↗
Mechanism of Action

Sunitinib is a small molecule that inhibits multiple RTKs, some of which are implicated in tumor growth, pathologic angiogenesis, and metastatic progression of cancer. Sunitinib was evaluated for its inhibitory activity against a variety of kinases (>80 kinases) and was identified as an inhibitor of platelet-derived growth factor receptors (PDGFRa and PDGFRb), vascular endothelial growth factor receptors (VEGFR1, VEGFR2 and VEGFR3), stem cell factor receptor (KIT), Fms-like tyrosine kinase-3 (FLT3), colony stimulating factor receptor Type 1 (CSF-1R), and the glial cell-line derived neurotrophic factor receptor (RET). Sunitinib inhibition of the activity of these RTKs has been demonstrated in biochemical and cellular assays, and inhibition of function has been demonstrated in cell proliferation assays. The primary metabolite exhibits similar potency compared to sunitinib in biochemical and cellular assays.

Resistance Mutations — 9 resistance samples observed in COSMIC
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AC058822.1
p.D602V
FLT3
p.D835Y 5
LRP1B
p.C1187W
PDGFRA
p.D842V 5
TET2
p.P46L p.P67L

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

Details
DrugBank ID DB01268 ↗
Approval Date 2006-01-26
Molecular Weight 398.4738 g/mol
Drug Class EGFR Inhibitor
ATC Codes L01XE04
Synonyms Sunitinibum
SMILES
CCN(CC)CCNC(=O)C1=C(C)NC(\C=C2/C(=O)NC3=C2C=C(F)C=C3)=C1C
ADMET Profile
Computing properties…
Drug References (DrugBank)