SCHEMBL1927119

SCHEMBL1927119

COC(=O)c1cccc(Nc2nccc(-c3cccnc3)n2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABL1 P00519 18/20 1.00
BCR P11274 15/20 1.00
SRC P12931 9/20 1.00
PRKCA P17252 10/20 0.77
PRKCD Q05655 7/20 0.69
PDGFRB P09619 6/20 0.69
PDGFRA P16234 6/20 0.69
PRKD3 O94806 2/20 0.68
PRKCG P05129 2/20 0.68
PRKCB P05771 2/20 0.68
PRKCH P24723 2/20 0.68
PRKCI P41743 2/20 0.68
PRKCE Q02156 2/20 0.68
PRKCQ Q04759 2/20 0.68
PRKCZ Q05513 2/20 0.68
PRKD1 Q15139 2/20 0.68
EGFR P00533 5/20 0.64
PRKACA P17612 1/20 0.64
PRKACG P22612 1/20 0.64
PRKACB P22694 1/20 0.64

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
SCHEMBL1927060 0.89 ABL1 (0.80) ABL1BCRSRCPRKCAPRKCD
SCHEMBL7465138 0.88 ABL1 (0.80) ABL1BCRSRCPRKCAPRKCD
SCHEMBL8252396 0.87 ABL1 (0.77) ABL1BCRSRCPRKCAPRKCD
SCHEMBL1655099 0.87 ABL1 (1.00) ABL1BCRSRCPRKCAPRKCD
SCHEMBL27143326 0.86 ABL1 (0.76) ABL1BCRSRCPRKCAPRKCD
SCHEMBL4895454 0.86 ABL1 (0.80) ABL1BCRSRCPRKCAPRKCD
SCHEMBL14088818 0.86 ABL1 (0.80) ABL1BCRSRCPRKCAPRKCD
Hydrochloric Acid SCHEMBL27711429 0.85 ABL1 (0.79) ABL1BCRSRCPRKCAPRKCD
Hydrochloric Acid SCHEMBL27708725 0.84 ABL1 (0.77) ABL1BCRSRCPRKCAPRKCD
SCHEMBL534524 0.84 ABL1 (0.72) ABL1BCRSRCPRKCAPDGFRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005065074-A2 PROTECTION OF TISSUES AND CELLS FROM CYTOTOXIC EFFECTS OF IONIZING RADIATION BY ABL INHIBITORS TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2005-07-21 WO claimed
US-5516775-A TO INHIBIT PROTEIN KINASE C CIBA-GEIGY CORPORATION (US) 1996-05-14 US claimed
EP-0588762-A1 Use of pyrimidine derivatives as inhibitors of proteinkinase C and antitumor drugs CIBA-GEIGY AG (CH) 1994-03-23 EP claimed
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
EP-1532138-B1 INHIBITORS OF TYROSINE KINASES NOVARTIS AG (CH) 2008-11-19 EP disclosed
CN-101045727-A Inhibitors of tyrosine kinases NOVARTIS AG (CH) 2007-10-03 CN disclosed
CN-1324022-C Tyrosine kinase inhibitors NOVARTIS AG (CH) 2007-07-04 CN 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
CN-1675195-A Tyrosine kinase inhibitors NOVARTIS AG (CH) 2005-09-28 CN disclosed
WO-2005065074-A2 PROTECTION OF TISSUES AND CELLS FROM CYTOTOXIC EFFECTS OF IONIZING RADIATION BY ABL INHIBITORS TEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2005-07-21 WO disclosed
US-5516775-A TO INHIBIT PROTEIN KINASE C CIBA-GEIGY CORPORATION (US) 1996-05-14 US disclosed
EP-0588762-A1 Use of pyrimidine derivatives as inhibitors of proteinkinase C and antitumor drugs CIBA-GEIGY AG (CH) 1994-03-23 EP 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 (4 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 28/4885SRC 8/4885
US-20110218187-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885SRC 8/4885
US-20090286821-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 ABL1 1/4885BCR 28/4885SRC 8/4885
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 181/4885SRC 159/4885

“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.