SCHEMBL4767481

SCHEMBL4767481

CCOC(=O)C(Cc1cnc(Nc2ccccc2)nc1Nc1ccccc1)c1ccccc1OC

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PTK2 Q05397 1/20 0.49
MAPK8 P45983 1/20 0.48
MAPK9 P45984 1/20 0.48
EGFR P00533 7/20 0.46
JAK3 P52333 2/20 0.46
BTK Q06187 4/20 0.45
AURKA O14965 4/20 0.45
MAPT P10636 1/20 0.44
ITK Q08881 3/20 0.44
ULK1 O75385 1/20 0.42
CDK4 P11802 1/20 0.41
CDK2 P24941 1/20 0.41
SIRT5 Q9NXA8 1/20 0.41

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
SCHEMBL4771570 0.93 MAPK8 (0.50) PTK2MAPK8MAPK9EGFRJAK3
SCHEMBL4825515 0.91 MAPK8 (0.48) PTK2MAPK8MAPK9EGFRJAK3
SCHEMBL4773873 0.90 MAPK8 (0.51) PTK2MAPK8MAPK9EGFRJAK3
SCHEMBL4767520 0.87 MAPK8 (0.54) PTK2MAPK8MAPK9EGFRJAK3
SCHEMBL4771563 0.85 EGFR (0.49) MAPK8MAPK9EGFRJAK3BTK
SCHEMBL4770474 0.83 EGFR (0.47) PTK2EGFRJAK3BTKAURKA
SCHEMBL4771780 0.82 EGFR (0.46) PTK2EGFRJAK3BTKAURKA
SCHEMBL4775725 0.81 CDK2 (0.49) PTK2MAPK8MAPK9JAK3BTK
SCHEMBL4770594 0.81 MAPK9 (0.51) PTK2MAPK8MAPK9EGFRJAK3
SCHEMBL4769925 0.80 AURKA (0.48) PTK2MAPK8MAPK9EGFRJAK3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7098332-B2 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones HOFFMANN-LA ROCHE INC. (US) 2006-08-29 US claimed
EP-1581531-A1 PYRIDINO[2,3-D]PYRIMIDINE DERIVATIVES AS SELECTIIVE KDR AND FGFR INHIBITORS F. Hoffmann-La Roche AG (CH) 2005-10-05 EP claimed
WO-2004056822-A1 PYRIDINO `2, 3-D! PYRIMIDINE DERIVATIVES AS SELECTIVE KDR AND FGFR INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2004-07-08 WO claimed
US-20040122029-A1 Novel dihydropyridinone compounds LIU JIN-JUN (US) 2004-06-24 US claimed
EP-1581531-B1 PYRIDINO¬2,3-D PYRIMIDINE DERIVATIVES AS SELECTIIVE KDR AND FGFR INHIBITORS HOFFMANN LA ROCHE (CH) 2008-02-27 EP disclosed
US-7098332-B2 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones HOFFMANN-LA ROCHE INC. (US) 2006-08-29 US disclosed
EP-1581531-A1 PYRIDINO[2,3-D]PYRIMIDINE DERIVATIVES AS SELECTIIVE KDR AND FGFR INHIBITORS F. Hoffmann-La Roche AG (CH) 2005-10-05 EP disclosed
WO-2004056822-A1 PYRIDINO `2, 3-D! PYRIMIDINE DERIVATIVES AS SELECTIVE KDR AND FGFR INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2004-07-08 WO disclosed
US-20040122029-A1 Novel dihydropyridinone compounds LIU JIN-JUN (US) 2004-06-24 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 (1 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-20040122029-A1 Novel dihydropyridinone compounds FGFR1, FGFR3, FGFR4 PTK2 41/4885MAPK8 477/4885MAPK9 536/4885

“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.