SCHEMBL3539441

SCHEMBL3539441

O=C(O)c1cc(F)c(F)c(F)c1Cl

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 2/20 0.52
NFE2L2 Q16236 1/20 0.52
CYP3A4 P08684 1/20 0.44
CES2 O00748 3/20 0.39
CES1 P23141 3/20 0.39
KDM4E B2RXH2 1/20 0.38
ASPH Q12797 1/20 0.38
KDM8 Q8N371 1/20 0.38
TSHR P16473 2/20 0.38
ALDH1A1 P00352 2/20 0.38
TP53 P04637 1/20 0.38
CASP1 P29466 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
DAO P14920 1/20 0.38
CA1 P00915 2/20 0.36
CA2 P00918 2/20 0.36
AKR1C2 P52895 2/20 0.36
AKR1C1 Q04828 2/20 0.36
ALB P02768 1/20 0.36
AKR1C4 P17516 1/20 0.36

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
SCHEMBL8373793 0.87 KEAP1 (0.52) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL10472704 0.83 KEAP1 (0.48) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL29376622 0.83 KEAP1 (0.52) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL22972614 0.83 KEAP1 (0.52) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL2434231 0.83 KEAP1 (0.52) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL10617307 0.82 KEAP1 (0.47) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL10626987 0.82 KEAP1 (0.47) KEAP1NFE2L2CYP3A4KDM4EASPH
Hydrochloric Acid SCHEMBL10563667 0.81 KEAP1 (0.50) KEAP1NFE2L2CYP3A4CES2CES1
SCHEMBL8974977 0.80 KEAP1 (0.53) KEAP1NFE2L2CYP3A4KDM4EASPH
Fluoride SCHEMBL6445071 0.79 KEAP1 (0.47) KEAP1NFE2L2CES2CES1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0682008-B1 Substituted 2-chloro-3,4,5-trifluorobenzenes and process for their preparation CLARIANT GMBH (DE) 1998-12-30 EP claimed
EP-0682008-A1 Substituted 2-chloro-3,4,5-trifluorobenzenes and process for their preparation HOECHST AKTIENGESELLSCHAFT (DE) 1995-11-15 EP claimed
JP-4187656-A None JP disclosed
JP-8040990-A None JP disclosed
US-7700585-B2 Derivatives of N-[phenyl(pyrrolidine-2-YL)methyl]benzamide and N-[(azepan-2-YL) phenylmethyl]benzamide, preparation method thereof and application of same in therapeutics SANOFI-AVENTIS (FR) 2010-04-20 US disclosed
WO-2008018639-A2 GLYCINE TRANSPORTER INHIBITOR TAISHO PHARMACEUTICAL CO., LTD. (JP) 2008-02-14 WO disclosed
US-20070208006-A1 DERIVATIVES OF N-[PHENYL(PYRROLIDINE-2-YL)METHYL]BENZAMIDE AND N-[(AZEPAN-2-YL)PHENYLMETHYL]BENZAMIDE, PREPARATION METHOD THEREOF AND APPLICATION OF SAME IN THERAPEUTICS SANOFI-AVENTIS (FR) 2007-09-06 US disclosed
US-7226917-B2 Derivatives of N-[phenyl(pyrrolidine-2-yl)methyl]benzamide and N-[(azepan-2-yl)phenylmethyl]benzamide, preparation, and use in treatment of schizophrenia SANOFI-AVENTIS (FR) 2007-06-05 US disclosed
CN-1882534-A Derivatives of N- [ phenyl (2-pyrrolidinyl) methyl ] benzamide and N- [ (2-azepanyl) phenylmethyl ] benzamide, preparation and therapeutic use thereof SANOFI AVENTIS (FR) 2006-12-20 CN disclosed
US-20060223802-A1 Derivatives of N-[phenyl(pyrrolidine-2-yl)methyl]benzamide and N-[(azepan-2-yl)phenylmethyl]benzamide, preparation method thereof and application of same in therapeutics SANOFI-AVENTIS (FR) 2006-10-05 US disclosed
EP-0757028-B1 Process for the preparation of aromatic carbonic acid esters CLARIANT GMBH (DE) 1999-12-29 EP disclosed
US-5739388-A Process for the preparation of aromatic compounds by decarboxylation of aromatic carboxylic acids HOECHST AKTIENGESELLSCHAFT (DE) 1998-04-14 US disclosed
EP-0811601-A1 Process for the preparation of aromatic carbonic acid esters Clariant GmbH (DE) 1997-12-10 EP disclosed
EP-0757028-A1 Process for the preparation of aromatic carbonic acid esters HOECHST AKTIENGESELLSCHAFT (DE) 1997-02-05 EP disclosed
US-5565612-A Substituted 2-chloro-3,4,5-trifluorobenzenes and a process for their preparation HOECHST AKTIENGESELLSCHAFT (DE) 1996-10-15 US disclosed
JP-H0840990-A SUBSTITUTED 2-CHLORO-3,4,5-TRIFLUOROBENZENE AND ITS PRODUCTION HOECHST AG 1996-02-13 JP disclosed
US-5481032-A Process for the preparation of halogenated benzoic acids HOECHST AKTIENGESELLSCHAFT (DE) 1996-01-02 US disclosed
CN-1112917-A Substituted 2-chloro-3,4,5-trifluorobenzenes and a process for their preparation HOECHST AG (DE) 1995-12-06 CN disclosed
EP-0682008-A1 Substituted 2-chloro-3,4,5-trifluorobenzenes and process for their preparation HOECHST AKTIENGESELLSCHAFT (DE) 1995-11-15 EP disclosed
JP-H04187656-A NOVEL 2-CHLORO-3,4,5-TRIFLUOROBENZOIC ACIDS SEIMI CHEM KK 1992-07-06 JP 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 (2 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-20070208006-A1 DERIVATIVES OF N-[PHENYL(PYRROLIDINE-2-YL)METHYL]BENZAMIDE AND N-[(AZEPAN-2-YL)PHENYLMETHYL]BENZAMIDE, PREPARATION METHOD THEREOF AND APPLICATION OF SAME IN THERAPEUTICS SNCA, CHRNA10, CHRNA5 KEAP1 2901/4885NFE2L2 1584/4885CYP3A4 2925/4885
US-20060223802-A1 Derivatives of N-[phenyl(pyrrolidine-2-yl)methyl]benzamide and N-[(azepan-2-yl)phenylmethyl]benzamide, preparation method thereof and application of same in therapeutics SNCA, CHRNA10, CHRNA5 KEAP1 2901/4885NFE2L2 1584/4885CYP3A4 2925/4885

“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.