SCHEMBL344663

SCHEMBL344663

CC(=O)Oc1cc(F)c(F)cc1F

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP4F2 P78329 2/20 0.55
CYP4A11 Q02928 2/20 0.55
TNFSF11 O14788 1/20 0.44
KDM4E B2RXH2 4/20 0.42
ALDH1A1 P00352 3/20 0.42
TSHR P16473 3/20 0.42
RAB9A P51151 2/20 0.42
GAA P10253 1/20 0.42
CFD P00746 2/20 0.41
HPGD P15428 2/20 0.40
HSD17B10 Q99714 2/20 0.40
USP2 O75604 1/20 0.40
CYP2C19 P33261 1/20 0.40
ESR1 P03372 1/20 0.39
ITGB3 P05106 1/20 0.39
ITGA2B P08514 1/20 0.39
HMGB1 P09429 1/20 0.39
GGT1 P19440 1/20 0.39
PTGS1 P23219 1/20 0.39
PTGS2 P35354 1/20 0.39

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
SCHEMBL29140951 0.98 CYP4F2 (0.53) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL24445868 0.85 CYP4F2 (0.50) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL24436700 0.85 CYP4F2 (0.50) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL28133983 0.84 CYP4F2 (0.49) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL12768204 0.83 ACHE (0.49) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL24436814 0.83 CYP4F2 (0.47) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL28782428 0.81 KDM4E (0.46) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL12768196 0.81 CYP4F2 (0.46) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL13074358 0.79 CYP4F2 (0.45) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1
SCHEMBL12727395 0.79 CFD (0.58) CYP4F2CYP4A11TNFSF11KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111393282-A Preparation method of 2,4, 5-trifluorophenylacetic acid 湖南复瑞生物医药技术有限责任公司 2020-07-10 CN claimed
US-10483466-B2 P-doping cross-linking of organic hole transporters SIEMENS AKTIENGESELLSCHAFT (DE) 2019-11-19 US claimed
EP-3114715-B1 P-DOPING CROSS-LINKING OF ORGANIC HOLE TRANSPORTERS SIEMENS AG (DE) 2019-10-30 EP claimed
US-20180198069-A1 P-Doping Cross-Linking Of Organic Hole Transporters SIEMENS AKTIENGESELLSCHAFT (DE) 2018-07-12 US claimed
CN-105949072-A Preparation method and intermediate of beta-substituted amino-gamma-substituted aryl butyric acid 苏州敬业医药化工有限公司 2016-09-21 CN claimed
EP-2331545-A2 IMPROVED PROCESS FOR PREPARATION OF (2R)-4-OXO-4-[3- (TRIFLUOROMETHYL)-5,6-DIHYDRO [1,2,4]-TRIAZOLO[4,3-A]PYRAZIN- 7(8H)-YL]-L-(2,4,5-TRIFLUOROPHENYL)BUTAN-2-AMINE&NEW IMPURITIES IN PREPARATION THEREOF Cadila Healthcare Limited (IN) 2011-06-15 EP claimed
WO-2010032264-A2 IMPROVED PROCESS FOR PREPARATION OF (2R)-4-OXO-4-[3- (TRIFLUOROMETHYL)-5,6-DIHYDRO [1,2,4]-TRIAZOLO[4,3-A]PYRAZIN- 7(8H)-YL]-L-(2,4,5-TRIFLUOROPHENYL)BUTAN-2-AMINE & NEW IMPURITIES IN PREPARATION THEREOF CADILA HEALTHCARE LIMITED (IN) 2010-03-25 WO claimed
US-12509421-B2 Preparation and application of deuterated 4-phenyl-4-piperidinols NANCHANG DOUBLE ANGEL BIOTECHNOLOGY DEVELOPMENT CO., LTD. (CN) 2025-12-30 US disclosed
US-20250304534-A1 Preparation and Application of Deuterated 4-Phenyl-4-Piperidinols NANCHANG DOUBLE ANGEL BIOTECHNOLOGY DEVELOPMENT CO., LTD. (CN) 2025-10-02 US disclosed
CN-120154006-A Application of p-fluorobenzaldehyde and composition containing p-fluorobenzaldehyde in attracting cotton bollworms 中国农业科学院植物保护研究所 2025-06-17 CN disclosed
CN-117384029-B Synthesis method of 2,4, 5-trifluoro phenylacetic acid 山东国邦药业有限公司 2024-02-20 CN disclosed
CN-117384029-A Synthesis method of 2,4, 5-trifluoro phenylacetic acid 山东国邦药业有限公司 2024-01-12 CN disclosed
CN-116478169-A Synthesis method of sitagliptin 黑龙江岭润生物科技有限公司 2023-07-25 CN disclosed
EP-1798250-A2 Molecules suitable for binding to a metal layer for covalently immobilizing biomolecules INTERUNIVERSITAIR MICROELEKTRONICA CENTRUM vzw (IMEC) (BE) 2007-06-20 EP disclosed
CN-1845674-A Novel crystalline forms of a phosphoric acid salt of a dipeptidyl peptidase-iv inhibitor MERCK & CO INC (US) 2006-10-11 CN disclosed
CN-1761642-A Process for the preparation of chiral beta-amino acid derivatives by asymmetric hydrogenation MERCK & CO INC (US) 2006-04-19 CN disclosed
US-20040068141-A1 Process for the synthesis of trifluorophenylacetic acids ARMSTRONG JOSEPH D (US) 2004-04-08 US disclosed
EP-1077701-A4 ANTI-VIRAL COMPOUNDS LILLY CO ELI (US) 2002-03-20 EP disclosed
EP-1077701-A1 ANTI-VIRAL COMPOUNDS ELI LILLY AND COMPANY (US) 2001-02-28 EP disclosed
WO-1999059587-A1 ANTI-VIRAL COMPOUNDS ELI LILLY AND COMPANY (US) 1999-11-25 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 (3 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-20040068141-A1 Process for the synthesis of trifluorophenylacetic acids PCCA, PAH, PFAS CYP4F2 17/4885CYP4A11 302/4885TNFSF11 4849/4885
US-20250304534-A1 Preparation and Application of Deuterated 4-Phenyl-4-Piperidinols DHPS, OPRL1, QDPR CYP4F2 562/4885CYP4A11 159/4885TNFSF11 4852/4885
US-12509421-B2 Preparation and application of deuterated 4-phenyl-4-piperidinols OPRD1, OPRK1, OPRL1 CYP4F2 858/4885CYP4A11 229/4885TNFSF11 4748/4885

“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.