SCHEMBL1169878

SCHEMBL1169878

COC(=O)c1cc(NCCc2ccc(C(F)(F)F)cc2)ccc1O

nearest known ligand 0.52

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
EGFR P00533 6/20 0.52
NOX4 Q9NPH5 1/20 0.51
RORC P51449 2/20 0.46
SYK P43405 3/20 0.45
CFTR P13569 1/20 0.45
MAPT P10636 1/20 0.45
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
CA7 P43166 1/20 0.44
CA9 Q16790 1/20 0.44
CA14 Q9ULX7 1/20 0.44
CNR1 P21554 1/20 0.44
FFAR1 O14842 1/20 0.44
KDM4E B2RXH2 1/20 0.44
P2RX1 P51575 1/20 0.43
P2RX4 Q99571 1/20 0.43
P2RX7 Q99572 1/20 0.43
TMPRSS4 Q9NRS4 1/20 0.43

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
SCHEMBL3417227 0.89 CNR1 (0.46) EGFRNOX4RORCSYKCNR1
SCHEMBL608498 0.86 KDM4C (0.53) EGFRNOX4RORCSYKMAPT
SCHEMBL12863172 0.86 EGFR (0.55) EGFRNOX4SYKMAPTCA12
SCHEMBL4116154 0.85 KDM4C (0.52) EGFRNOX4RORCSYKMAPT
Potassium Ion SCHEMBL4116152 0.84 RORC (0.47) RORCSYKCA12CA1CA2
SCHEMBL11937520 0.84 KDM4E (0.43) EGFRRORCCFTRCNR1FFAR1
SCHEMBL11937518 0.82 NLRP3 (0.59) RORCMAPTP2RX4
Sulfuric Acid SCHEMBL1170031 0.82 PPARA (0.49) EGFRNOX4RORCSYKMAPT
SCHEMBL12877595 0.81 EGFR (0.55) EGFRRORCSYKMAPTCNR1
SCHEMBL26181060 0.80 RORC (0.45) EGFRRORCCFTRCA12CA1

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2215050-B1 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS NEUROTECH PHARMACEUTICALS CO LTD (KR) 2012-06-27 EP claimed
US-20110028757-A1 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS NEUROTECH PHARMACEUTICALS CO., LTD. (KR) 2011-02-03 US claimed
EP-2215050-A2 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS Neurotech Pharmaceuticals Co., Ltd. (KR) 2010-08-11 EP claimed
WO-2009064084-A2 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS NEUROTECH CO., LTD. (KR) 2009-05-22 WO claimed
EP-4261201-A1 METHOD FOR PREPARING 2-HYDROXY-5-[2-(4-(TRIFLUOROMETHYLPHENYL)ETHYLAMINO)]BENZOIC ACID GNT Pharma Co., Ltd (KR) 2023-10-18 EP disclosed
WO-2022121853-A1 METHOD FOR PREPARING 2-HYDROXY-5-[2-(4-(TRIFLUOROMETHYLPHENYL)ETHYLAMINO)]BENZOIC ACID 吉恩特药业株式会社 2022-06-16 WO disclosed
EP-2215050-B1 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS NEUROTECH PHARMACEUTICALS CO LTD (KR) 2012-06-27 EP disclosed
US-20110028757-A1 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS NEUROTECH PHARMACEUTICALS CO., LTD. (KR) 2011-02-03 US 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 (1 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-20110028757-A1 MANUFACTURING METHOD OF 2-HYDROXY-5-PHENYLALKYLAMINOBENZOIC ACID DERIVATIVES AND THEIR SALTS PAH, HACL2, HAAO EGFR 1211/4885NOX4 3427/4885RORC 4505/4885

“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.