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Drug ReportsLinifanib
Linifanib
Linifanib is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
20 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C809110
CarcinomaD002277C80.0213
AdenocarcinomaD000230112
Hepatocellular carcinomaD006528C22.0112
Liver neoplasmsD008113EFO_1001513C22.0112
Liver diseasesD008107HP_0002910K70-K7711
Gastrointestinal neoplasmsD005770C26.911
Digestive system neoplasmsD00406711
Gastrointestinal diseasesD00576711
Neoplasms by histologic typeD00937011
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Non-small-cell lung carcinomaD002289123
Lung neoplasmsD008175HP_0100526C34.90123
EndometriosisD004715EFO_0001065N80111
Colorectal neoplasmsD01517911
Macular degenerationD008268EFO_0001365H35.3011
Breast neoplasmsD001943EFO_0003869C5011
Renal cell carcinomaD002292EFO_000037611
RecurrenceD01200811
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
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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
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 908 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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51 adverse events reported
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