SCHEMBL2245947

SCHEMBL2245947

CCNS(=O)(=O)c1cccc(-c2nc(N)c3cc(-c4c(Cl)cccc4Cl)c(=O)n(OC)c3n2)c1

nearest known ligand 0.42

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ BRD4 O60885 6/20 0.42
▸ SYK P43405 2/20 0.35
▸ EGFR P00533 2/20 0.35
▸ FGFR1 P11362 2/20 0.35
▸ SRC P12931 1/20 0.34
▸ FGFR2 P21802 1/20 0.34
▸ FGFR4 P22455 1/20 0.34
▸ FGFR3 P22607 1/20 0.34
▸ RIPK2 O43353 1/20 0.33
▸ ACVR1 Q04771 1/20 0.33
▸ NOD2 Q9HC29 1/20 0.33
▸ PIK3CA P42336 1/20 0.33
▸ PIK3CB P42338 1/20 0.33
▸ PIK3CG P48736 1/20 0.33
▸ VCAM1 P19320 1/20 0.33
▸ TARS1 P26639 1/20 0.33

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
SCHEMBL2245139 0.91 BRD4 (0.45) BRD4SYKFGFR1
SCHEMBL2359361 0.91 NR1H2 (0.37) SYKEGFRFGFR1SRCFGFR2
SCHEMBL2245930 0.88 RIPK2 (0.41) EGFRFGFR1SRCFGFR2FGFR4
SCHEMBL2245977 0.87 LMNA (0.42) EGFRFGFR1SRCFGFR2FGFR4
SCHEMBL2252104 0.82 HSP90AA1 (0.43) BRD4EGFRSRCACVR1PIK3CA
SCHEMBL2253187 0.82 BRD4 (0.45) BRD4SYK
SCHEMBL2246715 0.81 FGFR1 (0.39) EGFRFGFR1SRCFGFR2FGFR4
SCHEMBL2246030 0.81 FGFR1 (0.38) BRD4EGFRFGFR1SRCFGFR2
SCHEMBL2244321 0.81 DGAT1 (0.37) BRD4EGFRFGFR1SRCFGFR2
SCHEMBL2250539 0.79 HAVCR2 (0.41) EGFRFGFR1SRCFGFR2FGFR4

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-20140163223-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-20140163004-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-20140163003-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-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-20140163007-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 — — US disclosed
US-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 — — US disclosed
US-20140163006-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-8518958-B2 Pyrido [2,3-D] pyrimidines and their use as kinase inhibitors FORMA THERAPEUTICS, INC. (US) 2013-08-27 — — 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 (8 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 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163007-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163222-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20140163223-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 BRD4 606/4885SYK 793/4885EGFR 816/4885
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS DCK, PDXK, TK1 BRD4 661/4885SYK 728/4885EGFR 887/4885

“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.

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