SCHEMBL1656154

SCHEMBL1656154

Cc1ccc(C(=O)Nc2ccc(Cl)cc2)cc1Nc1nccc(-c2cccnc2)n1

nearest known ligand 0.90

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
PDGFRA P16234 13/20 0.90
ABL1 P00519 12/20 0.90
BCR P11274 7/20 0.90
PDGFRB P09619 5/20 0.90
KIT P10721 7/20 0.76
EGFR P00533 1/20 0.75
PRKCA P17252 1/20 0.75
KDR P35968 1/20 0.69

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
SCHEMBL9677 0.94 PDGFRA (1.00) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL1927373 0.92 ABL1 (0.82) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL1654378 0.92 ABL1 (0.82) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL8282185 0.91 PDGFRA (0.93) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL1929404 0.91 ABL1 (0.80) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL1654172 0.91 PDGFRA (0.79) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL1653493 0.89 ABL1 (0.77) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL11927817 0.88 PDGFRA (0.92) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL3973176 0.88 ABL1 (0.82) PDGFRAABL1BCRPDGFRBKIT
SCHEMBL3219611 0.87 PDGFRA (0.83) PDGFRAABL1BCRPDGFRBKIT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070129389-A1 Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders NOVARTIS AG (CH) 2007-06-07 US claimed
US-20200368267-A1 PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR AMYOTROPHIC LATERAL SCLEROSIS KYOTO UNIVERSITY (JP) 2020-11-26 US disclosed
EP-2606890-A1 Combinations comprising BCR-ABL/C-KIT/PDGF-R TK inhibitors for treating cancer Novartis AG (CH) 2013-06-26 EP disclosed
US-20120252811-A1 COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER BURKE GREGORY PETER (US) 2012-10-04 US disclosed
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
EP-2314297-A1 Combinations comprising bcr-abl/c-kit/pdgf-r tk inhibitors for treating cancer Novartis AG (CH) 2011-04-27 EP disclosed
US-7687512-B2 4-Methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide; for neurodegenerative diseases like Alzheimer's disease, Down's Syndrome, memory and cognitive impairment, dementia, amyloid neuropathies, brain inflammation, nerve and brain trauma NOVARTIS AG (CH) 2010-03-30 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
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-20070129389-A1 Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders NOVARTIS AG (CH) 2007-06-07 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
CN-1675195-A Tyrosine kinase inhibitors NOVARTIS AG (CH) 2005-09-28 CN 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 (7 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 PDGFRA 382/4885ABL1 1/4885BCR 28/4885
US-20110218187-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 PDGFRA 382/4885ABL1 1/4885BCR 28/4885
US-20120252811-A1 COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER KIT, ABL1, PDGFRB PDGFRA 4/4885ABL1 2/4885BCR 8/4885
US-20070129389-A1 Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders TIE1, ABL2, FYN PDGFRA 5/4885ABL1 19/4885BCR 62/4885
US-20200368267-A1 PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR AMYOTROPHIC LATERAL SCLEROSIS SMN1; SMN2, SOD1, CAPNS1 PDGFRA 545/4885ABL1 228/4885BCR 1806/4885
US-20080188451-A1 INHIBITORS OF TYROSINE KINASES ABL1, BTK, FLT3 PDGFRA 382/4885ABL1 1/4885BCR 28/4885
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 PDGFRA 440/4885ABL1 1/4885BCR 181/4885

“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.