SCHEMBL177479

SCHEMBL177479

OB(O)c1cc(F)c(F)c(F)c1

nearest known ligand 0.50

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CES2 O00748 2/20 0.42
CES1 P23141 2/20 0.42
ENPP2 Q13822 4/20 0.35
CA4 P22748 3/20 0.35
CA6 P23280 1/20 0.35
CA5A P35218 1/20 0.35
CA7 P43166 1/20 0.35
CA14 Q9ULX7 1/20 0.35
CA5B Q9Y2D0 1/20 0.35
CA1 P00915 3/20 0.33
CA2 P00918 3/20 0.33
MGLL Q99685 2/20 0.33
KDM4E B2RXH2 1/20 0.32
ALDH1A1 P00352 1/20 0.32

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
SCHEMBL28703625 0.97 CES2 (0.40) CES2CES1ENPP2CA4CA6
SCHEMBL15649887 0.85 ENPP2 (0.33) CES2CES1ENPP2CA6CA5A
SCHEMBL16374001 0.83 TTR (0.41) CES2CES1ENPP2
SCHEMBL16384322 0.83 CA2 (0.36) CES2CES1CA2
SCHEMBL9939130 0.83 ALDH1A1 (0.35) CES2CES1ENPP2KDM4EALDH1A1
SCHEMBL1804144 0.82 ORAI1 (0.43) CES2CES1CA4CA1CA2
SCHEMBL1277215 0.80 ERN1 (0.38) ENPP2CA4CA6CA5ACA7
SCHEMBL28824846 0.80 ENPP2 (0.33) ENPP2CA4CA6CA5ACA7
SCHEMBL18090905 0.79 ERN1 (0.39) CES2CES1CA4CA1CA2
SCHEMBL28736451 0.79 MGLL (0.39) MGLL

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 1371 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119591560-B Synthesis method of thifluzamide 湖南速博生物技术有限公司 2025-04-29 CN claimed
WO-2025074340-A1 A PROCESS FOR PREPARATION OF AMINOBIPHENYL COMPOUNDS AND INTERMEDIATES THEREOF UPL LIMITED (IN) 2025-04-10 WO claimed
CN-119591560-A Synthesis method of thifluzamide 湖南速博生物技术有限公司 2025-03-11 CN claimed
CN-119504448-A Synthesis method of 3',4',5' -trifluoro-2-aminobiphenyl 河北八亿时空药业有限公司 2025-02-25 CN claimed
CN-119236835-B Continuous reaction system and continuous method for producing 3',4',5' -trifluoro-biphenyl-2-amine 天津凯莱英医药科技发展有限公司 2025-02-25 CN claimed
CN-116217354-B Efficient green synthesis method and product of liquid crystal monomer 烟台德润液晶材料有限公司 2025-02-11 CN claimed
CN-119236835-A Continuous reaction system and continuous method for producing 3',4',5' -trifluoro-biphenyl-2-amine 天津凯莱英医药科技发展有限公司 2025-01-03 CN claimed
WO-2025006693-A1 CANNABIDIOL-LIKE COMPOUNDS AND METHODS FOR THE SELECTIVE PREPARATION OF THE SAME UNIVERSITY OF MISSISSIPPI (US) 2025-01-02 WO claimed
CN-119019319-A Synthesis method of N, N' -bis 2, 6-tetramethyl-4-piperidinyl-1, 3-phthalamide 浙江诺驷新材料科技有限公司 2024-11-26 CN claimed
CN-118307475-B Preparation method of stable isotope labeled fluxapyroxad internal standard reagent 谱同生物医药科技(常州)有限公司 2024-11-22 CN claimed
US-20100040538-A1 Polymer Systems for Lung Volume Reduction Therapy CANADIAN IMPERIAL BANK OF COMMERCE (CA) 2010-02-18 US claimed
EP-2107067-A1 Boron catalysed peptide synthesis DSM IP Assets B.V. (NL) 2009-10-07 EP claimed
EP-2081946-A2 ADENOSINE DERIVATIVES FOR THE TREATMENT OF PAIN Biovitrum AB (publ) (SE) 2009-07-29 EP claimed
EP-2059227-A2 POLYMER SYSTEMS FOR LUNG VOLUME REDUCTION THERAPY Aeris Therapeutics, Inc. (US) 2009-05-20 EP claimed
WO-2008039827-A2 POLYMER SYSTEMS FOR LUNG VOLUME REDUCTION THERAPY AERIS THERAPEUTICS, INC. (US) 2008-04-03 WO claimed
WO-2008000745-A2 ADENOSINE DERIVATIVES FOR THE TREATMENT OF PAIN BIOVITRUM AB (PUBL) (SE) 2008-01-03 WO claimed
US-7037905-B2 Pharmaceutical use of boronic acids and esters thereof NOVO NORDISK A/S (DK) 2006-05-02 US claimed
US-20040053889-A1 Pharmaceutical use of boronic acids and esters thereof NOVO NORDISK A/S (DK) 2004-03-18 US claimed
WO-2003105860-A1 PHARMACEUTICAL USE OF BORONIC ACIDS AND ESTERS THEREOF NOVO NORDISK A/S (DK) 2003-12-24 WO claimed
EP-1277755-A1 OPTICALLY ACTIVE QUATERNARY AMMONIUM SALT WITH AXIAL ASYMMETRY, PROCESS FOR PRODUCING THE SAME, AND APPLICATION TO ASYMMETRIC SYNTHESIS OF $g(a)-AMINO ACID DERIVATIVE Nagase & Co., Ltd. (JP) 2003-01-22 EP claimed

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-20040053889-A1 Pharmaceutical use of boronic acids and esters thereof LIPE, CEL, LIPA CES2 18/4885CES1 9/4885ENPP2 998/4885
US-20100040538-A1 Polymer Systems for Lung Volume Reduction Therapy GFER, MUC1, CTH CES2 1317/4885CES1 1971/4885ENPP2 854/4885

“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.