Linifanib

Linifanib

SCHEMBL2239943

CCO.Cc1ccc(F)c(NC(=O)Nc2ccc(-c3cccc4[nH]nc(N)c34)cc2)c1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CSF1RFLT1FLT3FLT4KDRPDGFRAPDGFRB

The experimentally established mechanism targets of Linifanib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR known ✓ P35968 19/20 0.94
FLT3 known ✓ P36888 16/20 0.94
CSF1R known ✓ P07333 10/20 0.94
FLT4 known ✓ P35916 10/20 0.94
FLT1 known ✓ P17948 9/20 0.94
PDGFRB known ✓ P09619 1/20 0.94
PDGFRA known ✓ P16234 1/20 0.94
KIT P10721 14/20 0.94
LYN P07948 7/20 0.94
SRC P12931 6/20 0.94
BLK P51451 6/20 0.94
AURKA O14965 5/20 0.94
AURKB Q96GD4 5/20 0.94
PLK4 O00444 4/20 0.94
ROCK2 O75116 4/20 0.94
MET P08581 4/20 0.94
PRKACA P17612 4/20 0.94
RPS6KB1 P23443 4/20 0.94
CSNK1D P48730 4/20 0.94
STK3 Q13188 4/20 0.94

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Linifanib SCHEMBL93804 0.97 KDR (1.00) KDRFLT3KITCSF1RFLT4
Linifanib SCHEMBL29375368 0.97 KDR (1.00) KDRFLT3KITCSF1RFLT4
Linifanib SCHEMBL1880038 0.96 KDR (0.98) KDRFLT3KITCSF1RFLT4
Alcohol SCHEMBL16817140 0.89 KDR (0.80) KDRFLT3KITCSF1RFLT4
SCHEMBL423390 0.88 KDR (0.77) KDRFLT3KITCSF1RFLT4
SCHEMBL421934 0.88 KDR (0.82) KDRFLT3KITCSF1RFLT4
Alcohol SCHEMBL16817141 0.88 KDR (0.81) KDRFLT3KITCSF1RFLT4
SCHEMBL422778 0.87 KDR (1.00) KDRFLT3KITCSF1RFLT4
SCHEMBL420765 0.87 KDR (1.00) KDRFLT3KITCSF1RFLT4
SCHEMBL16303695 0.87 KDR (0.78) KDRFLT3KITCSF1RFLT4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7994208-B2 Crystalline chemotherapeutic ABBOTT LABORATORIES (US) 2011-08-09 US claimed
EP-2195300-A1 CRYSTALLINE CHEMOTHERAPEUTIC Abbott Laboratories (US) 2010-06-16 EP claimed
US-20090105326-A1 Crystalline Chemotherapeutic ABBOTT LABORATORIES (US) 2009-04-23 US claimed
WO-2009052225-A1 CRYSTALLINE CHEMOTHERAPEUTIC ABBOTT LABORATORIES (US) 2009-04-23 WO claimed
EP-2195300-B1 CRYSTALLINE CHEMOTHERAPEUTIC ABBVIE BAHAMAS LTD (BS) 2015-06-24 EP disclosed
US-7994208-B2 Crystalline chemotherapeutic ABBOTT LABORATORIES (US) 2011-08-09 US disclosed
US-7994208-B2 Crystalline chemotherapeutic ABBOTT LABORATORIES (US) 2011-08-09 US disclosed
EP-2195300-A1 CRYSTALLINE CHEMOTHERAPEUTIC Abbott Laboratories (US) 2010-06-16 EP disclosed
EP-2195300-A1 CRYSTALLINE CHEMOTHERAPEUTIC Abbott Laboratories (US) 2010-06-16 EP disclosed
US-20100143459-A1 PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION OF TYROSINE KINASE INHIBITOR ABBOTT GMBH & CO. KG (DE) 2010-06-10 US disclosed
EP-2089003-A1 PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION OF TYROSINE KINASE INHIBITOR Abbott GmbH & Co. KG (DE) 2009-08-19 EP disclosed
WO-2009100176-A2 PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION OF TYROSINE KINASE INHIBITOR ABBOTT LABORATORIES (US) 2009-08-13 WO disclosed
US-20090203709-A1 Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor ABBOTT LABORATORIES (US) 2009-08-13 US disclosed
US-20090105326-A1 Crystalline Chemotherapeutic ABBOTT LABORATORIES (US) 2009-04-23 US disclosed
US-20090105326-A1 Crystalline Chemotherapeutic ABBOTT LABORATORIES (US) 2009-04-23 US disclosed
WO-2009052225-A1 CRYSTALLINE CHEMOTHERAPEUTIC ABBOTT LABORATORIES (US) 2009-04-23 WO disclosed
WO-2009052225-A1 CRYSTALLINE CHEMOTHERAPEUTIC ABBOTT LABORATORIES (US) 2009-04-23 WO disclosed
WO-2008055966-A1 PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION OF TYROSINE KINASE INHIBITOR ABBOTT GMBH & CO. KG (DE) 2008-05-15 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090203709-A1 Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor SRC, LYN, SYK KDR 144/4885FLT3 9/4885CSF1R 537/4885
US-20100143459-A1 PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION OF TYROSINE KINASE INHIBITOR SRC, LYN, SYK KDR 144/4885FLT3 9/4885CSF1R 537/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.