SCHEMBL2248643

SCHEMBL2248643

COC(=O)c1ccc(-c2nc(N)c3cc(-c4c(Cl)cccc4Cl)c(=O)n(OC)c3n2)cc1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FGFR1 P11362 3/20 0.39
▸ RHEB Q15382 1/20 0.38
▸ SMN1; SMN2 Q16637 2/20 0.38
▸ KDM4E B2RXH2 1/20 0.38
▸ NPC1 O15118 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ RAB9A P51151 1/20 0.38
▸ KMT2A Q03164 1/20 0.38
▸ MAPK14 Q16539 5/20 0.37
▸ RORC P51449 1/20 0.37
▸ EGFR P00533 1/20 0.37
▸ SRC P12931 1/20 0.37
▸ FGFR2 P21802 1/20 0.37
▸ FGFR4 P22455 1/20 0.37
▸ FGFR3 P22607 1/20 0.37
▸ CNR1 P21554 1/20 0.37
▸ ALDH1A1 P00352 1/20 0.36
▸ HPGD P15428 1/20 0.36
▸ TP53 P04637 1/20 0.36
▸ DHFR P00374 1/20 0.36

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
SCHEMBL2246053 0.87 CNR1 (0.39) FGFR1MAPK14EGFRSRCFGFR2
SCHEMBL2250006 0.85 SRC (0.37) FGFR1MAPK14EGFRSRCFGFR2
SCHEMBL2248966 0.84 FGFR1 (0.41) FGFR1MAPK14EGFRSRCFGFR2
SCHEMBL2249966 0.84 FGFR1 (0.36) FGFR1MAPK14EGFRSRCFGFR2
SCHEMBL2251464 0.84 PIK3CA (0.41) FGFR1EGFRSRCFGFR2FGFR4
SCHEMBL2247940 0.83 FGFR1 (0.40) FGFR1EGFRSRCFGFR2FGFR4
SCHEMBL2251461 0.83 CNR1 (0.37) FGFR1EGFRSRCFGFR2FGFR4
SCHEMBL2251394 0.83 FGFR1 (0.36) FGFR1MAPK14EGFRSRCFGFR2
SCHEMBL2244321 0.82 DGAT1 (0.37) FGFR1SMN1; SMN2KDM4ERORCEGFR
SCHEMBL2252397 0.82 FGFR1 (0.37) FGFR1MAPK14EGFRSRCFGFR2

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-20140163006-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-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-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-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-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 — — US disclosed
US-20140163222-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-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors FORMA THERAPEUTICS, INC. (US) 2014-06-12 — — US disclosed
US-20140163223-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 (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 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20140163003-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20140163005-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20140163222-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20140163004-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20140163223-A1 Pyrido-[2,3-D] Pyrimidines and Their Use as Kinase Inhibitors DCK, PDXK, CDK2 FGFR1 745/4885RHEB 3475/4885SMN1; SMN2 3440/4885
US-20110201594-A1 PYRIDO [2,3-D] PYRIMIDINES AND THEIR USE AS KINASE INHIBITORS DCK, PDXK, TK1 FGFR1 818/4885RHEB 3465/4885SMN1; SMN2 3453/4885

“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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