SCHEMBL2055590

SCHEMBL2055590

COc1cc2c(Nc3ccc(C)cc3F)ncnc2cc1OCC1CCN(C(=O)OC(C)(C)C)CC1

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 17/20 0.75
EGFR P00533 16/20 0.75
FGFR1 P11362 13/20 0.75
FLT1 P17948 13/20 0.75
FLT4 P35916 13/20 0.75
PDGFRB P09619 2/20 0.63
TEK Q02763 2/20 0.63
EPHA2 P29317 2/20 0.63
EPHB4 P54760 2/20 0.63
RET P07949 2/20 0.63
KIF5B P33176 2/20 0.63
BMPR1B O00238 1/20 0.63
PLK4 O00444 1/20 0.63
CIT O14578 1/20 0.63
GAK O14976 1/20 0.63
EPHB6 O15197 1/20 0.63
RIPK2 O43353 1/20 0.63
ROCK2 O75116 1/20 0.63
STK10 O94804 1/20 0.63
MAP4K4 O95819 1/20 0.63

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
SCHEMBL1614506 0.93 KDR (0.75) KDREGFRFGFR1FLT1FLT4
SCHEMBL17179598 0.88 KDR (0.65) KDREGFRFGFR1FLT1FLT4
SCHEMBL1781194 0.88 KDR (0.67) KDREGFRFGFR1FLT1FLT4
SCHEMBL2136770 0.86 EGFR (1.00) KDREGFRFGFR1FLT1FLT4
SCHEMBL3131165 0.85 EGFR (0.75) KDREGFREPHA2EPHB4RET
SCHEMBL2136853 0.85 KDR (0.74) KDREGFRFGFR1FLT1FLT4
SCHEMBL2136783 0.85 EGFR (0.74) KDREGFRFGFR1FLT1FLT4
SCHEMBL13617552 0.84 KDR (0.75) KDREGFRFGFR1FLT1FLT4
SCHEMBL3152430 0.82 KDR (0.80) KDREGFRFGFR1FLT1FLT4
SCHEMBL13163378 0.82 KDR (0.75) 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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210276972-A1 Quinazoline Derivatives as VEGF Inhibitors GENZYME CORPORATION (US) 2021-09-09 US disclosed
US-20200262811-A1 Quinazoline Derivatives as VEGF Inhibitors GENZYME CORPORATION (US) 2020-08-20 US disclosed
US-10457664-B2 Quinazoline derivatives as VEGF inhibitors GENZYME CORPORATION (US) 2019-10-29 US disclosed
US-20190002433-A1 Quinazoline Derivatives as VEGF Inhibitors GENZYME CORPORATION (US) 2019-01-03 US disclosed
US-20180118716-A1 Chemical Process GENZYME CORPORATION (US) 2018-05-03 US disclosed
US-20180099946-A1 Quinazoline Derivatives as VEGF Inhibitors GENZYME CORPORATION (US) 2018-04-12 US disclosed
US-9815816-B2 Chemical process for the synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2017-11-14 US disclosed
US-20160185754-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline ASTRAZENECA AB (SE) 2016-06-30 US disclosed
US-20160130249-A1 Quinazoline Derivatives as VEGF Inhibitors ASTRAZENECA AB (SE) 2016-05-12 US disclosed
US-9040548-B2 Quinazoline derivatives as VEGF inhibitors ASTRAZENECA AB (SE) 2015-05-26 US disclosed
US-8642608-B2 Quinazoline derivatives as VEGF inhibitors ASTRAZENECA AB (SE) 2014-02-04 US disclosed
US-8163926-B2 Process for the synthesis of piperidinyl sulphonate esters ASTRAZENECA AB (SE) 2012-04-24 US disclosed
US-20120095229-A1 CHEMICAL PROCESS GENZYME CORPORATION 2012-04-19 US disclosed
US-20110065736-A1 QUINAZOLINE DERIVATIVES AS VEGF INHIBITORS ASTRAZENECA AB (SE) 2011-03-17 US disclosed
US-20090203905-A1 CHEMICAL PROCESS GENZYME CORPORATION 2009-08-13 US disclosed
EP-1676845-B1 New quinazoline derivatives ASTRAZENECA AB (SE) 2008-06-11 EP disclosed
US-20070265286-A1 Quinazoline derivatives as VEGF inhibitors ASTRAZENECA AB 2007-11-15 US disclosed
US-7173038-B1 Quinazoline derivatives as VEGF inhibitors ASTRAZENECA AB (SE) 2007-02-06 US disclosed
EP-1676845-A1 New quinazoline derivatives AstraZeneca AB (SE) 2006-07-05 EP disclosed
EP-1244647-B1 QUINAZOLINE DERIVATIVES AS VEGF INHIBITORS ASTRAZENECA AB (SE) 2006-06-21 EP 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 (12 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-20180099946-A1 Quinazoline Derivatives as VEGF Inhibitors FLT4, FLT1, KDR KDR 3/4885EGFR 199/4885FGFR1 161/4885
US-20210276972-A1 Quinazoline Derivatives as VEGF Inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 207/4885FGFR1 154/4885
US-20110065736-A1 QUINAZOLINE DERIVATIVES AS VEGF INHIBITORS FLT1, FLT4, KDR KDR 3/4885EGFR 183/4885FGFR1 143/4885
US-10457664-B2 Quinazoline derivatives as VEGF inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 179/4885FGFR1 196/4885
US-20090203905-A1 CHEMICAL PROCESS CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885FGFR1 2764/4885
US-20070265286-A1 Quinazoline derivatives as VEGF inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 183/4885FGFR1 143/4885
US-20160130249-A1 Quinazoline Derivatives as VEGF Inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 181/4885FGFR1 135/4885
US-20160185754-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline CYP3A4, CYP3A7, CYP4B1 KDR 3217/4885EGFR 3838/4885FGFR1 2445/4885
US-20200262811-A1 Quinazoline Derivatives as VEGF Inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 181/4885FGFR1 135/4885
US-20190002433-A1 Quinazoline Derivatives as VEGF Inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 179/4885FGFR1 196/4885
US-20120095229-A1 CHEMICAL PROCESS CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885FGFR1 2764/4885
US-20180118716-A1 Chemical Process CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885FGFR1 2764/4885

“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.