SCHEMBL1927486

SCHEMBL1927486

Cc1ccc(C(=O)N2CCN(c3ccccn3)CC2)cc1Nc1nccc(-c2cccnc2)n1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABL1 P00519 13/20 0.59
BCR P11274 11/20 0.59
PDGFRA P16234 11/20 0.57
PDGFRB P09619 7/20 0.57
EGFR P00533 5/20 0.56
PRKCA P17252 3/20 0.56
KDR P35968 2/20 0.53
KIT P10721 4/20 0.52
PLK4 O00444 1/20 0.52
DDX3X O00571 1/20 0.52
GAK O14976 1/20 0.52
SLC22A2 O15244 1/20 0.52
MAPK13 O15264 1/20 0.52
CA12 O43570 1/20 0.52
SLC22A3 O75751 1/20 0.52
ABCB11 O95342 1/20 0.52
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
LMNA P02545 1/20 0.52
ALB P02768 1/20 0.52

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
SCHEMBL1927247 0.92 ABL1 (0.60) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL23244322 0.90 ABL1 (0.57) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL29576184 0.90 ABL1 (0.57) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1926491 0.88 ABL1 (0.61) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1926859 0.85 ABL1 (0.62) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1927769 0.85 ABL1 (0.61) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1928951 0.85 ABL1 (0.57) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1930036 0.84 ABL1 (0.68) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1927307 0.83 ABL1 (0.60) ABL1BCRPDGFRAPDGFRBEGFR
SCHEMBL1927978 0.83 PDGFRA (0.66) ABL1BCRPDGFRAPDGFRBEGFR

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2368889-A1 Inhibitors of tyrosine kinases Novartis AG (CH) 2011-09-28 EP disclosed
US-20110218187-A1 INHIBITORS OF TYROSINE KINASES BREITENSTEIN WERNER 2011-09-08 US disclosed
EP-2357182-A1 Inhibitors of tyrosine kinases Novartis AG (CH) 2011-08-17 EP disclosed
US-7956053-B2 Inhibitors of tyrosine kinases NOVARTIS AG (CH) 2011-06-07 US disclosed
US-20090286821-A1 INHIBITORS OF TYROSINE KINASES BREITENSTEIN WERNER 2009-11-19 US disclosed
EP-2100891-A1 Inhibitors of tyrosine kinases Novartis AG (CH) 2009-09-16 EP disclosed
US-7569566-B2 4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol1yl)-3-(trifluoromethyl)phenyl]benzamide or an N-oxide or salts; anticarcinogenic agent (leukaemia) NOVARTIS AG (CH) 2009-08-04 US disclosed
US-20080188451-A1 INHIBITORS OF TYROSINE KINASES BREITENSTEIN WERNER 2008-08-07 US disclosed
US-20070093506-A1 Inhibitors of tyrosine kinases BREITENSTEIN WERNER 2007-04-26 US disclosed
US-7169791-B2 Inhibitors of tyrosine kinases NOVARTIS AG (CH) 2007-01-30 US disclosed
US-20060167015-A1 4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol1yl)-3-(trifluoromethyl)phenyl]benzamide or an N-oxide or salts; anticarcinogenic agent (leukaemia) NOVARTIS AG (CH) 2006-07-27 US 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-20070093506-A1 Inhibitors of tyrosine kinases ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885PDGFRA 382/4885
US-20110218187-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885PDGFRA 382/4885
US-20080188451-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885PDGFRA 382/4885
US-20090286821-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885PDGFRA 382/4885
US-20060167015-A1 4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol1yl)-3-(trifluoromethyl)phenyl]benzamide or an N-oxide or salts; anticarcinogenic agent (leukaemia) ABL1, CDK2, CDKN1A ABL1 1/4885BCR 181/4885PDGFRA 440/4885

“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.