SCHEMBL2248056

SCHEMBL2248056

COn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(Nc3ccc(C(C)=O)cc3)nc21

nearest known ligand 0.64

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SRC P12931 14/20 0.64
PDGFRB P09619 10/20 0.64
PDGFRA P16234 10/20 0.64
ABL1 P00519 9/20 0.64
MAPK14 Q16539 9/20 0.64
FGFR1 P11362 12/20 0.63
EGFR P00533 7/20 0.62
KIT P10721 4/20 0.60
WEE1 P30291 3/20 0.60
FGFR2 P21802 2/20 0.60
FGFR4 P22455 2/20 0.60
FGFR3 P22607 2/20 0.60

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
SCHEMBL12367950 0.94 SRC (0.57) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2248640 0.93 FGFR1 (0.68) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL14221896 0.92 SRC (0.62) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2249826 0.89 FGFR1 (0.76) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2249068 0.88 FGFR1 (0.76) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2248039 0.88 FGFR1 (0.66) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL14222154 0.88 FGFR1 (0.66) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2246051 0.87 SRC (0.67) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2252578 0.87 FGFR1 (0.76) SRCPDGFRBPDGFRAABL1MAPK14
SCHEMBL2252859 0.85 SRC (0.79) SRCPDGFRBPDGFRAABL1MAPK14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-20140163223-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-20140163006-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-20140163222-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US claimed
US-8518958-B2 Pyrido [2,3-D] pyrimidines and their use as kinase inhibitors FORMA THERAPEUTICS, INC. (US) 2013-08-27 US claimed
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS Valo Health, LLC 2011-08-18 US claimed
EP-2084159-A1 PYRIDO Ý2, 3-D¨PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS GPC Biotech Inc. (US) 2009-08-05 EP claimed
WO-2008047307-A1 PYRIDO [2, 3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS GPC BIOTECH INC. (US) 2008-04-24 WO claimed
US-20140163222-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US disclosed
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US disclosed
US-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US disclosed
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US disclosed
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 US disclosed
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS Valo Health, LLC 2011-08-18 US disclosed
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS Valo Health, LLC 2011-08-18 US disclosed
EP-2084159-A1 PYRIDO Ý2, 3-D¨PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS GPC Biotech Inc. (US) 2009-08-05 EP disclosed
WO-2008150260-A1 8-OXY-2-AMINOPYRIDO (2, 3-D) PYRIMIDIN-7-ONE DERIVATIVES AS KINASE INHIBITORS AND ANTICANCER AGENTS GPC BIOTECH, INC. (US) 2008-12-11 WO disclosed
WO-2008047307-A1 PYRIDO [2, 3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS GPC BIOTECH INC. (US) 2008-04-24 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 (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-20140163006-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20140163222-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20140163223-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 SRC 605/4885PDGFRB 362/4885PDGFRA 399/4885
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS DCK, PDXK, TK1 SRC 664/4885PDGFRB 365/4885PDGFRA 421/4885

“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.