SCHEMBL273582

SCHEMBL273582

Nc1nccc(Oc2ccc3c(C(=O)O)cccc3c2)n1

nearest known ligand 0.63

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
KDR P35968 20/20 0.63
FLT1 P17948 3/20 0.63
FLT4 P35916 2/20 0.63
RET P07949 2/20 0.63
PDGFRB P09619 1/20 0.63
KIT P10721 1/20 0.63
AURKA O14965 3/20 0.47
MET P08581 3/20 0.47
TEK Q02763 3/20 0.47
AURKB Q96GD4 3/20 0.47
ABL1 P00519 1/20 0.47
LCK P06239 1/20 0.47
LYN P07948 1/20 0.47

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
SCHEMBL5740759 0.93 KDR (0.59) KDRFLT1FLT4RETPDGFRB
SCHEMBL272837 0.86 KDR (0.56) KDRFLT1FLT4RETPDGFRB
SCHEMBL2748909 0.86 KDR (0.67) KDRFLT1FLT4RETPDGFRB
SCHEMBL4548727 0.86 KDR (0.78) KDRFLT1FLT4RETPDGFRB
SCHEMBL2747970 0.85 KDR (0.55) KDRFLT1FLT4RETPDGFRB
SCHEMBL5740763 0.83 KDR (0.58) KDRFLT1FLT4RETPDGFRB
SCHEMBL3582067 0.83 KDR (0.53) KDRFLT1FLT4RETPDGFRB
SCHEMBL10260360 0.83 KDR (0.61) KDRFLT1FLT4RETPDGFRB
SCHEMBL273408 0.83 KDR (0.63) KDRFLT1FLT4RETPDGFRB
SCHEMBL2708711 0.83 KDR (0.64) KDRFLT1FLT4RETPDGFRB

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 45 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2574340-A2 Combination comprising a pyrimidylaminobenzamide compound and a THR315LLEe kinase inhibitor Novartis AG (CH) 2013-04-03 EP claimed
EP-2007391-B1 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR NOVARTIS AG (CH) 2012-12-19 EP claimed
US-20110301157-A1 BICYCLIC AMIDES AS KINASE INHIBITORS NOVARTIS AG 2011-12-08 US claimed
US-20090286803-A1 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR NOVARTIS AG (CH) 2009-11-19 US claimed
EP-2007391-A2 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR Novartis AG (CH) 2008-12-31 EP claimed
WO-2007116029-A2 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR NOVARTIS AG (CH) 2007-10-18 WO claimed
EP-2574340-A2 Combination comprising a pyrimidylaminobenzamide compound and a THR315LLEe kinase inhibitor Novartis AG (CH) 2013-04-03 EP disclosed
EP-2007391-B1 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR NOVARTIS AG (CH) 2012-12-19 EP disclosed
US-20120172386-A1 Combinations Comprising a VEGF Receptor Inhibitor NOVARTIS AG (CH) 2012-07-05 US disclosed
US-20120172386-A1 Combinations Comprising a VEGF Receptor Inhibitor NOVARTIS AG (CH) 2012-07-05 US disclosed
US-20120172386-A1 Combinations Comprising a VEGF Receptor Inhibitor NOVARTIS AG (CH) 2012-07-05 US disclosed
US-20120122857-A1 HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES NOVARTIS AG (CH) 2012-05-17 US disclosed
US-8178557-B2 Compounds and methods of use AMGEN INC. (US) 2012-05-15 US disclosed
EP-1794149-A2 BICYCLIC AMIDES AS KINASE INHIBITORS Novartis AG (CH) 2007-06-13 EP disclosed
WO-2007031265-A2 COMBINATIONS COMPRISING A VEGF RECEPTOR INHIBITOR AND A PENETRATION ENHANCER NOVARTIS AG (CH) 2007-03-22 WO disclosed
WO-2007031265-A2 COMBINATIONS COMPRISING A VEGF RECEPTOR INHIBITOR AND A PENETRATION ENHANCER NOVARTIS AG (CH) 2007-03-22 WO disclosed
US-20060241115-A1 Compounds and methods of use AMGEN INC. 2006-10-26 US disclosed
EP-1713484-A2 COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2006-10-25 EP disclosed
WO-2006059234-A2 BICYCLIC AMIDES AS KINASE INHIBITORS NOVARTIS AG (CH) 2006-06-08 WO disclosed
WO-2005070891-A2 COMPOUNDS AND METHODS OF USE AMGEN INC (US) 2005-08-04 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 (5 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-20060241115-A1 Compounds and methods of use HGF, HGFAC, MET KDR 354/4885FLT1 89/4885FLT4 125/4885
US-20110301157-A1 BICYCLIC AMIDES AS KINASE INHIBITORS MAP3K20, MAP3K1, MAP3K19 KDR 826/4885FLT1 638/4885FLT4 944/4885
US-20120172386-A1 Combinations Comprising a VEGF Receptor Inhibitor KDR, FLT4, FLT1 KDR 1/4885FLT1 3/4885FLT4 2/4885
US-20090286803-A1 COMBINATION COMPRISING A) A PYRIMIDYLAMINOBENZAMIDE COMPOUND, AND B) A THR315LLE KINASE INHIBITOR MAP3K5, CHEK2, CDK2 KDR 651/4885FLT1 615/4885FLT4 505/4885
US-20120122857-A1 HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES MAP3K20, PHKG1, PHKG2 KDR 1319/4885FLT1 1353/4885FLT4 1993/4885

“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.