SCHEMBL198544

SCHEMBL198544

COc1cc2nccc(Oc3ccc(NC(=O)c4c(Nc5ccncc5)ccn(Cc5ccccc5)c4=O)nc3)c2cc1OC

nearest known ligand 0.83

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
PTK2B Q14289 10/20 0.83
PTK2 Q05397 5/20 0.73
SYK P43405 1/20 0.71
EIF2AK3 Q9NZJ5 2/20 0.60
MET P08581 7/20 0.58
IGF1R P08069 1/20 0.58
KDR P35968 1/20 0.58
EIF2AK4 Q9P2K8 1/20 0.57

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
SCHEMBL200667 0.96 PTK2B (0.86) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL200775 0.93 PTK2B (0.78) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL199896 0.91 PTK2B (1.00) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL199676 0.89 PTK2B (0.85) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL198735 0.86 PTK2B (0.80) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL197872 0.85 PTK2B (0.80) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL199176 0.84 PTK2B (1.00) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL201320 0.83 PTK2B (0.79) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL199485 0.80 MET (0.78) PTK2BPTK2SYKEIF2AK3MET
SCHEMBL199798 0.79 SYK (0.81) PTK2BPTK2SYKEIF2AK3MET

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140243339-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2014-08-28 US claimed
US-20120070413-A1 METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES KIM TAE-SEONG (US) 2012-03-22 US claimed
US-8088794-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2012-01-03 US claimed
US-20110229469-A1 METHODS FOR THE TREATMENT OF CANCER LUDWIG INSTITUTE FOR CANCER RESEARCH (US) 2011-09-22 US claimed
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE AMGEN INC. (US) 2011-05-19 US claimed
US-20110104161-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. 2011-05-05 US claimed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US claimed
US-20140243339-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2014-08-28 US disclosed
EP-1881976-B1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS AMGEN INC (US) 2012-10-17 EP disclosed
EP-1881976-B1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS AMGEN INC (US) 2012-10-17 EP disclosed
US-20120070413-A1 METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES KIM TAE-SEONG (US) 2012-03-22 US disclosed
US-20120070413-A1 METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES KIM TAE-SEONG (US) 2012-03-22 US disclosed
US-8088794-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2012-01-03 US disclosed
US-20110104161-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. 2011-05-05 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-7858623-B2 Substituted amide derivatives and methods of use AMGEN INC. (US) 2010-12-28 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 US disclosed
US-20080312232-A1 Substituted amide derivatives and methods of use AMGEN INC. (US) 2008-12-18 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 (6 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-20110104161-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER MET, HGF, HDGF PTK2B 194/4885PTK2 411/4885SYK 548/4885
US-20080312232-A1 Substituted amide derivatives and methods of use HGF, HGFAC, MET PTK2B 1450/4885PTK2 1543/4885SYK 1944/4885
US-20120070413-A1 METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES HGF, HGFAC, MET PTK2B 1646/4885PTK2 1834/4885SYK 1811/4885
US-20110229469-A1 METHODS FOR THE TREATMENT OF CANCER MET, HGF, EGFR PTK2B 216/4885PTK2 122/4885SYK 1677/4885
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE HGF, HGFAC, MET PTK2B 1450/4885PTK2 1543/4885SYK 1944/4885
US-20140243339-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER MET, HGF, HDGF PTK2B 191/4885PTK2 419/4885SYK 619/4885

“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.