SCHEMBL156289

SCHEMBL156289

COc1cc2c(Nc3ccc(Br)cc3F)ncnc2cc1O

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 15/20 0.83
EGFR P00533 9/20 0.83
RET P07949 6/20 0.83
KIF5B P33176 6/20 0.83
FLT1 P17948 10/20 0.66
FGFR1 P11362 8/20 0.66
FLT4 P35916 6/20 0.64
EPHB2 P29323 2/20 0.64
RAF1 P04049 2/20 0.61
BRAF P15056 2/20 0.61
PDGFRB P09619 3/20 0.60
FGFR2 P21802 2/20 0.60
FGFR4 P22455 2/20 0.60
FGFR3 P22607 2/20 0.60
TEK Q02763 2/20 0.60
BMPR1B O00238 1/20 0.60
PLK4 O00444 1/20 0.60
CIT O14578 1/20 0.60
GAK O14976 1/20 0.60
EPHB6 O15197 1/20 0.60

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
Hydrochloric Acid SCHEMBL28007000 0.99 KDR (0.81) KDREGFRRETKIF5BFLT1
SCHEMBL5241456 0.95 KDR (0.83) KDREGFRRETKIF5BFLT1
SCHEMBL1781767 0.92 KDR (0.71) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL29372105 0.92 KDR (0.70) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL2089050 0.92 KDR (0.70) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL28007015 0.91 KDR (0.69) KDREGFRRETKIF5BFLT1
SCHEMBL5864525 0.91 KDR (1.00) KDREGFRRETKIF5BFLT1
Hydrochloric Acid SCHEMBL7864775 0.90 KDR (0.98) KDREGFRRETKIF5BFLT1
SCHEMBL2055589 0.89 RAF1 (0.76) KDREGFRRETKIF5BFLT1
SCHEMBL1467058 0.88 KDR (0.83) KDREGFRRETKIF5BFLT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240150317-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2024-05-09 US claimed
US-20220033377-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2022-02-03 US claimed
US-10457664-B2 Quinazoline derivatives as VEGF inhibitors GENZYME CORPORATION (US) 2019-10-29 US claimed
US-10344015-B2 Chemical process for the synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2019-07-09 US claimed
US-20180118716-A1 Chemical Process GENZYME CORPORATION (US) 2018-05-03 US claimed
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 claimed
US-20140378684-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline ASTRAZENECA AB (SE) 2014-12-25 US claimed
US-20120095229-A1 CHEMICAL PROCESS GENZYME CORPORATION 2012-04-19 US claimed
EP-1943240-B1 CHEMICAL PROCESS ASTRAZENECA AB (SE) 2009-11-11 EP claimed
US-20090203905-A1 CHEMICAL PROCESS GENZYME CORPORATION 2009-08-13 US claimed
EP-1943240-A2 CHEMICAL PROCESS Astra Zeneca AB (SE) 2008-07-16 EP claimed
WO-2007036713-A2 CHEMICAL PROCESS ASTRAZENECA AB (SE) 2007-04-05 WO claimed
US-20240150317-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2024-05-09 US disclosed
WO-2024025991-A1 METHODS FOR DIAGNOSIS AND TREATMENT OF PULMONARY HYPERTENSION THE METHODIST HOSPITAL SYSTEM (US) 2024-02-01 WO disclosed
US-20220033377-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2022-02-03 US disclosed
US-20220033377-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2022-02-03 US disclosed
EP-0929530-A1 QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ZENECA LIMITED (GB) 1999-07-21 EP disclosed
EP-0885198-A1 4-ANILINOQUINAZOLINE DERIVATIVES ZENECA LIMITED (GB) 1998-12-23 EP disclosed
WO-1998013354-A1 QUINAZOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ZENECA LIMITED (GB) 1998-04-02 WO disclosed
WO-1997032856-A1 4-ANILINOQUINAZOLINE DERIVATIVES ZENECA LIMITED (GB) 1997-09-12 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 (9 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-20140378684-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 3838/4885RET 3472/4885
US-10457664-B2 Quinazoline derivatives as VEGF inhibitors FLT1, FLT4, KDR KDR 3/4885EGFR 179/4885RET 509/4885
US-20220033377-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 3838/4885RET 3472/4885
US-20090203905-A1 CHEMICAL PROCESS CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885RET 2751/4885
US-20240150317-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 3838/4885RET 3472/4885
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 3838/4885RET 3472/4885
US-10344015-B2 Chemical process for the synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline CYP3A4, CYP3A7, CYP4B1 KDR 3258/4885EGFR 3911/4885RET 3396/4885
US-20120095229-A1 CHEMICAL PROCESS CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885RET 2751/4885
US-20180118716-A1 Chemical Process CYP3A4, CYP3A5, CYP3A7 KDR 3543/4885EGFR 3879/4885RET 2751/4885

“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.