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Linifanib
Linifanib is a small molecule pharmaceutical. It is currently being investigated in clinical studies. It is known to target vascular endothelial growth factor receptor 3, cyclin-dependent kinase 19, vascular endothelial growth factor receptor 1, macrophage colony-stimulating factor 1 receptor, proto-oncogene tyrosine-protein kinase receptor Ret, mast/stem cell growth factor receptor Kit, cyclin-dependent kinase 8, vascular endothelial growth factor receptor 2, receptor-type tyrosine-protein kinase FLT3, platelet-derived growth factor receptor beta, and angiopoietin-1 receptor.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
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HCPCS
No data
Clinical
Clinical Trials
20 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C809110
AdenocarcinomaD000230112
Liver neoplasmsD008113EFO_1001513C22.0112
Liver diseasesD008107EFO_0001421K70-K7711
Hepatocellular carcinomaD006528C22.011
Digestive system neoplasmsD00406711
Neoplasms by histologic typeD00937011
Neoplasms by siteD00937111
Glandular and epithelial neoplasmsD00937511
Digestive system diseasesD004066EFO_0000405K92.911
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289123
EndometriosisD004715EFO_0001065N80111
Colorectal neoplasmsD01517911
Macular degenerationD008268EFO_0001365H35.3011
Breast neoplasmsD001943EFO_0003869C5011
Renal cell carcinomaD00229211
Colonic neoplasmsD003110C1811
Rectal neoplasmsD01200411
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLINIFANIB
INNlinifanib
Description
Linifanib is a member of the class of phenylureas that is urea in which one of the nitrogens is substituted by a 2-fluoro-5-methylphenyl group, while the other is substituted by a p-(3-amino-1H-indazol-4-yl)phenyl group. It is a potent, selective inhibitor of vascular endothelial growth factor and platelet-derived growth factor receptor tyrosine kinases. It has a role as an antineoplastic agent, an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor and an angiogenesis inhibitor. It is an aromatic amine, a member of indazoles and a member of phenylureas.
Classification
Small molecule
Drug classangiogenesis inhibitors
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Cc1ccc(F)c(NC(=O)Nc2ccc(-c3cccc4[nH]nc(N)c34)cc2)c1
Identifiers
PDB
CAS-ID796967-16-3
RxCUI
ChEMBL IDCHEMBL223360
ChEBI ID
PubChem CID11485656
DrugBank
UNII IDCO93X137CW (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
FLT4
FLT4
CDK19
CDK19
FLT1
FLT1
CSF1R
CSF1R
RET
RET
KIT
KIT
CDK8
CDK8
KDR
KDR
FLT3
FLT3
PDGFRB
PDGFRB
TEK
TEK
Organism
Homo sapiens
Gene name
FLT4
Gene synonyms
VEGFR3
NCBI Gene ID
Protein name
vascular endothelial growth factor receptor 3
Protein synonyms
Feline McDonough Sarcoma (FMS)-like tyrosine kinase 4, FLT-4, fms related tyrosine kinase 4, Fms-like tyrosine kinase 4, primary congenital lymphedema, Tyrosine-protein kinase receptor FLT4, VEGF receptor-3
Uniprot ID
Mouse ortholog
Flt4 (14257)
vascular endothelial growth factor receptor 3 (P35917)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 767 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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49 adverse events reported
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