SCHEMBL197904

SCHEMBL197904

COc1cc2nccc(Oc3ccc(NC(=O)c4cc(Br)cn(Cc5ccccc5)c4=O)c(Cl)c3)c2cc1OC

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 9/20 0.61
MET P08581 9/20 0.61
SYK P43405 1/20 0.61
IGF1R P08069 1/20 0.61
PTK2B Q14289 2/20 0.55
PTK2 Q05397 1/20 0.53
PDGFRA P16234 2/20 0.51
RIPK2 O43353 1/20 0.51
STK10 O94804 1/20 0.51
ABL1 P00519 1/20 0.51
LCK P06239 1/20 0.51
LYN P07948 1/20 0.51
RET P07949 1/20 0.51
PDGFRB P09619 1/20 0.51
KIT P10721 1/20 0.51
BCR P11274 1/20 0.51
FGFR1 P11362 1/20 0.51
SRC P12931 1/20 0.51
FLT1 P17948 1/20 0.51
MAPK3 P27361 1/20 0.51

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
SCHEMBL198356 0.88 KDR (0.67) KDRMETIGF1RPTK2BPTK2
SCHEMBL200869 0.80 KDR (0.70) KDRMETSYKIGF1RPTK2B
SCHEMBL199798 0.79 SYK (0.81) KDRMETSYKIGF1RPTK2B
SCHEMBL10289174 0.78 MET (0.66) KDRMETPDGFRAPDGFRBAXL
SCHEMBL2742627 0.77 MET (0.64) KDRMETPDGFRAPDGFRBAXL
SCHEMBL200000 0.76 SYK (0.75) KDRMETSYKIGF1RPTK2B
SCHEMBL198114 0.76 MET (1.00) KDRMETIGF1RPDGFRARIPK2
SCHEMBL200020 0.76 PTK2B (0.79) KDRMETSYKIGF1RPTK2B
SCHEMBL200792 0.75 SYK (0.73) KDRMETSYKIGF1RPTK2B
SCHEMBL1878601 0.75 MET (0.77) KDRMETIGF1RPDGFRARIPK2

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 29 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
EP-2349328-A1 METHODS FOR THE TREATMENT OF CANCER LUDWIG INSTITUTE FOR CANCER RESEARCH (US) 2011-08-03 EP 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
WO-2010039248-A1 METHODS FOR THE TREATMENT OF CANCER LUDWIG INSTITUTE FOR CANCER RESEARCH (US) 2010-04-08 WO 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
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
WO-2010039248-A1 METHODS FOR THE TREATMENT OF CANCER LUDWIG INSTITUTE FOR CANCER RESEARCH (US) 2010-04-08 WO 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
EP-1881976-A1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS Amgen Inc., (US) 2008-01-30 EP disclosed
WO-2006116713-A1 SUBSTITUTED AMIDE DERIVATIVES AS PROTEIN KINASE INHIBITORS AMGEN INC. (US) 2006-11-02 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 (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 KDR 6/4885MET 1/4885SYK 548/4885
US-20080312232-A1 Substituted amide derivatives and methods of use HGF, HGFAC, MET KDR 200/4885MET 3/4885SYK 1944/4885
US-20120070413-A1 METHOD OF TREATING CANCER WITH SUBSTITUTED AMIDE DERIVATIVES HGF, HGFAC, MET KDR 304/4885MET 3/4885SYK 1811/4885
US-20110229469-A1 METHODS FOR THE TREATMENT OF CANCER MET, HGF, EGFR KDR 23/4885MET 1/4885SYK 1677/4885
US-20110118252-A1 SUBSTITUTED AMIDE DERIVATIVES AND METHODS OF USE HGF, HGFAC, MET KDR 200/4885MET 3/4885SYK 1944/4885
US-20140243339-A1 COMBINATIONS VEGF(R) INHIBITORS AND HEPATOCYTE GROWTH FACTOR (C-MET) INHIBITORS FOR THE TREATMENT OF CANCER MET, HGF, HDGF KDR 6/4885MET 1/4885SYK 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.