Trifluoroacetic Acid

Trifluoroacetic Acid

SCHEMBL2089050

COc1cc2c(Nc3ccc(Br)cc3F)ncnc2cc1O.O=C(O)C(F)(F)F

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 17/20 0.70
EGFR P00533 9/20 0.70
RET P07949 6/20 0.70
KIF5B P33176 6/20 0.70
FLT1 P17948 11/20 0.57
FGFR1 P11362 9/20 0.57
FLT4 P35916 7/20 0.55
EPHB2 P29323 2/20 0.55
RAF1 P04049 2/20 0.54
BRAF P15056 2/20 0.54
PDGFRB P09619 3/20 0.54
FGFR2 P21802 2/20 0.54
FGFR4 P22455 2/20 0.54
FGFR3 P22607 2/20 0.54
TEK Q02763 2/20 0.54
BMPR1B O00238 1/20 0.54
PLK4 O00444 1/20 0.54
CIT O14578 1/20 0.54
GAK O14976 1/20 0.54
EPHB6 O15197 1/20 0.54

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
Trifluoroacetic Acid SCHEMBL29372105 1.00 KDR (0.70) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL28007015 0.99 KDR (0.69) KDREGFRRETKIF5BFLT1
SCHEMBL156289 0.92 KDR (0.83) KDREGFRRETKIF5BFLT1
Hydrochloric Acid SCHEMBL28007000 0.91 KDR (0.81) KDREGFRRETKIF5BFLT1
SCHEMBL5241456 0.88 KDR (0.83) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL907480 0.85 KDR (0.57) KDREGFRRETKIF5BFLT1
SCHEMBL1781767 0.85 KDR (0.71) KDREGFRRETKIF5BFLT1
Trifluoroacetic Acid SCHEMBL907135 0.85 KDR (0.55) KDREGFRRETKIF5BFLT1
SCHEMBL2089052 0.85 KDR (0.77) KDREGFRRETKIF5BFLT1
Hydrochloric Acid SCHEMBL28007011 0.84 KDR (0.76) 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 23 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 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-3181554-B1 QUINAZOLINE DERIVATIVE CSPC ZHONGQI PHARMACEUTICAL TECH SHIJIAZHUANG CO LTD (CN) 2020-10-28 EP disclosed
US-10774079-B2 Quinazoline derivative CSPC ZHONGQI PHARMACEUTICAL TECHNOLOGY (SHIJIAZHUANG) CO., LTD. (CN) 2020-09-15 US disclosed
CN-106660970-B Quinazoline derivatives 石药集团中奇制药技术(石家庄)有限公司 2020-07-10 CN disclosed
US-10421754-B2 Quinazoline derivative CSPC ZHONGQI PHARMACEUTICAL TECHNOLOGY (SHIJIAZHUANG) CO., LTD. (CN) 2019-09-24 US disclosed
US-20190263782-A1 Chemical Process for the Synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline GENZYME CORPORATION (US) 2019-08-29 US disclosed
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 disclosed
US-20180118716-A1 Chemical Process GENZYME CORPORATION (US) 2018-05-03 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-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 disclosed
US-8865899-B2 Chemical process for the synthesis of 4-(4-bromo-2-fluoroanilino)-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline ASTRAZENECA AB (SE) 2014-10-21 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
EP-2053048-B1 Chemical in situ sulphonating process ASTRAZENECA AB (SE) 2010-09-15 EP disclosed
EP-1943240-B1 CHEMICAL PROCESS ASTRAZENECA AB (SE) 2009-11-11 EP disclosed
US-20090203905-A1 CHEMICAL PROCESS GENZYME CORPORATION 2009-08-13 US disclosed
EP-2053048-A1 Chemical in situ sulphonating process AstraZeneca AB (SE) 2009-04-29 EP disclosed
EP-1943240-A2 CHEMICAL PROCESS Astra Zeneca AB (SE) 2008-07-16 EP disclosed
WO-2007036713-A2 CHEMICAL PROCESS ASTRAZENECA AB (SE) 2007-04-05 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-10774079-B2 Quinazoline derivative H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, TOP2A, TOP1 KDR 3669/4885EGFR 3701/4885RET 4595/4885
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-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-10421754-B2 Quinazoline derivative H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, TOP2A, TOP1 KDR 3669/4885EGFR 3701/4885RET 4595/4885
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-20190263782-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.