SCHEMBL11517

SCHEMBL11517

COc1cc2ncnc(Nc3ccc(F)cc3F)c2cc1OCCCN1CCOCC1

nearest known ligand 0.84

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 13/20 0.84
EGFR P00533 9/20 0.84
FGFR1 P11362 7/20 0.84
FLT1 P17948 7/20 0.84
FLT4 P35916 6/20 0.84
SRC P12931 9/20 0.78
RET P07949 2/20 0.71
CIT O14578 1/20 0.71
GAK O14976 1/20 0.71
EPHB6 O15197 1/20 0.71
ABCC4 O15439 1/20 0.71
DAPK3 O43293 1/20 0.71
RIPK2 O43353 1/20 0.71
NR1I2 O75469 1/20 0.71
RPS6KA4 O75676 1/20 0.71
STK17B O94768 1/20 0.71
STK10 O94804 1/20 0.71
PRKD3 O94806 1/20 0.71
ABCB11 O95342 1/20 0.71
MAP4K4 O95819 1/20 0.71

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
SCHEMBL7867160 0.92 KDR (0.83) KDREGFRFGFR1FLT1FLT4
Hydrochloric Acid SCHEMBL7866060 0.92 KDR (0.84) KDREGFRFGFR1FLT1FLT4
SCHEMBL7857964 0.92 KDR (1.00) KDREGFRFGFR1FLT1FLT4
SCHEMBL22997455 0.91 KDR (0.81) KDREGFRFGFR1FLT1FLT4
Hydrochloric Acid SCHEMBL7870593 0.91 KDR (0.98) KDREGFRFGFR1FLT1FLT4
SCHEMBL7867735 0.89 KDR (0.78) KDREGFRFGFR1FLT1FLT4
SCHEMBL7866019 0.89 KDR (1.00) KDREGFRFGFR1FLT1FLT4
Hydrochloric Acid SCHEMBL7859597 0.89 KDR (0.77) KDREGFRFGFR1FLT1FLT4
SCHEMBL28424819 0.89 SRC (0.85) KDREGFRFGFR1FLT1FLT4
Hydrochloric Acid SCHEMBL7864803 0.88 KDR (0.98) KDREGFRFGFR1FLT1FLT4

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-5770599-A RECEPTOR TYROSINE KINASE INHIBITORS including 4-(3'-chloro-4'-fluoroanilino)-7-methoxy-6-(2-morpholinoethoxy)quinazoline (gefitinib) ZENECA LIMITED (GB) 1998-06-23 US claimed
US-20160303127-A1 COMBINATION THERAPY WITH C-MET AND EGFR ANTAGONISTS GENENTECH INC (US) 2016-10-20 US disclosed
US-20150086545-A1 COMBINATION THERAPY OF HER EXPRESSING TUMORS GENENTECH, INC. (US) 2015-03-26 US disclosed
US-20150056207-A1 COMBINATION THERAPY WITH C-MET AND EGFR ANTAGONISTS GENENTECH INC (US) 2015-02-26 US disclosed
US-20130005726-A1 COMPOSITIONS AND METHODS FOR TREATING INFLAMMATORY DISORDERS NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR NIH 2013-01-03 US disclosed
US-20120251530-A1 COMBINATION THERAPY OF HER EXPRESSING TUMORS SLIWKOWSKI MARK X (US) 2012-10-04 US disclosed
US-20120189573-A1 Methods of using death receptor agonists and EGFR inhibitors GENENTECH, INC. (US) 2012-07-26 US disclosed
US-8163287-B2 Combination therapy of her expressing tumors GENENTECH, INC. (US) 2012-04-24 US disclosed
US-20120094998-A1 Oligomer-Protein Tyrosine Kinase Inhibitor Conjugates NEKTAR THERAPEUTICS (US) 2012-04-19 US disclosed
US-20110262436-A1 TREATMENT METHOD GENENTECH, INC. (US) 2011-10-27 US disclosed
EP-1853300-A2 METHODS OF USING DEATH RECEPTOR AGONISTS AND EGFR INHIBITORS Genentech, Inc. (US) 2007-11-14 EP disclosed
WO-2007013950-A9 COMBINATION THERAPY OF HER EXPRESSING TUMORS GENENTECH INC (US) 2007-03-29 WO disclosed
WO-2007013950-A2 COMBINATION THERAPY OF HER EXPRESSING TUMORS GENENTECH, INC. (US) 2007-02-01 WO disclosed
US-20070020261-A1 Combination therapy of her expressing tumors GENENTECH, INC. 2007-01-25 US disclosed
WO-2006089015-A2 METHODS OF USING DEATH RECEPTOR AGONISTS AND EGFR INHIBITORS GENENTECH, INC. (US) 2006-08-24 WO disclosed
US-20060188498-A1 Methods of using death receptor agonists and EGFR inhibitors GENENTECH, INC. 2006-08-24 US disclosed
EP-0823900-B1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2000-12-27 EP disclosed
US-5770599-A RECEPTOR TYROSINE KINASE INHIBITORS including 4-(3'-chloro-4'-fluoroanilino)-7-methoxy-6-(2-morpholinoethoxy)quinazoline (gefitinib) ZENECA LIMITED (GB) 1998-06-23 US disclosed
EP-0823900-A1 QUINAZOLINE DERIVATIVES ZENECA LIMITED (GB) 1998-02-18 EP disclosed
WO-1996033980-A1 QUINAZOLINE DERIVATIVES ZENECA LIMITED (GB) 1996-10-31 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 (10 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-20120189573-A1 Methods of using death receptor agonists and EGFR inhibitors EGFR, ERBB4, TNFRSF9 KDR 50/4885EGFR 1/4885FGFR1 1140/4885
US-20150086545-A1 COMBINATION THERAPY OF HER EXPRESSING TUMORS ERBB2, EGFR, ERBB3 KDR 34/4885EGFR 2/4885FGFR1 47/4885
US-20060188498-A1 Methods of using death receptor agonists and EGFR inhibitors EGFR, ERBB4, TNFRSF9 KDR 50/4885EGFR 1/4885FGFR1 1140/4885
US-20070020261-A1 Combination therapy of her expressing tumors ERBB2, EGFR, ERBB3 KDR 34/4885EGFR 2/4885FGFR1 47/4885
US-20160303127-A1 COMBINATION THERAPY WITH C-MET AND EGFR ANTAGONISTS MET, EGFR, ERBB2 KDR 33/4885EGFR 2/4885FGFR1 19/4885
US-20110262436-A1 TREATMENT METHOD HGF, HDGF, FGF2 KDR 424/4885EGFR 6/4885FGFR1 14/4885
US-20150056207-A1 COMBINATION THERAPY WITH C-MET AND EGFR ANTAGONISTS MET, EGFR, ERBB2 KDR 33/4885EGFR 2/4885FGFR1 19/4885
US-20120094998-A1 Oligomer-Protein Tyrosine Kinase Inhibitor Conjugates PTK2B, ERBB2, FRK KDR 395/4885EGFR 129/4885FGFR1 462/4885
US-20130005726-A1 COMPOSITIONS AND METHODS FOR TREATING INFLAMMATORY DISORDERS NOD2, RIPK2, RIPK1 KDR 3236/4885EGFR 2498/4885FGFR1 2253/4885
US-20120251530-A1 COMBINATION THERAPY OF HER EXPRESSING TUMORS ERBB2, EGFR, ERBB3 KDR 34/4885EGFR 2/4885FGFR1 47/4885

“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.