SCHEMBL851355

SCHEMBL851355

O=C(O)C(O)c1cc(F)cc(F)c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 6/20 0.63
CES1 P23141 6/20 0.63
LMNA P02545 2/20 0.50
MAPK1 P28482 1/20 0.50
BLM P54132 2/20 0.39
NPSR1 Q6W5P4 1/20 0.39
TSHR P16473 1/20 0.39
CA12 O43570 1/20 0.36
CA1 P00915 1/20 0.36
CA9 Q16790 1/20 0.36
HCAR1 Q9BXC0 1/20 0.35
POLB P06746 1/20 0.34
PKM P14618 1/20 0.34
PTPN1 P18031 1/20 0.34
PTPN7 P35236 1/20 0.34
KMT2A Q03164 1/20 0.34
ESR2 Q92731 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
IDO1 P14902 1/20 0.34
TDO2 P48775 1/20 0.34

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
SCHEMBL1572867 1.00 CES2 (0.63) CES2CES1LMNAMAPK1BLM
SCHEMBL1572839 1.00 CES2 (0.63) CES2CES1LMNAMAPK1BLM
Hydrochloric Acid SCHEMBL7248840 0.98 CES2 (0.61) CES2CES1LMNAMAPK1BLM
Hydrochloric Acid SCHEMBL7248837 0.98 CES2 (0.61) CES2CES1LMNAMAPK1BLM
SCHEMBL23972859 0.86 CES2 (0.48) CES2CES1LMNAMAPK1BLM
SCHEMBL23972406 0.82 CES2 (0.46) CES2CES1LMNAMAPK1
SCHEMBL3344127 0.80 CES2 (0.47) CES2CES1LMNA
SCHEMBL7374087 0.80 CES2 (0.47) CES2CES1LMNA
SCHEMBL3344038 0.80 CES2 (0.47) CES2CES1LMNA
SCHEMBL8313497 0.79 CES2 (0.61) CES2CES1CA12CA1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118184679-A Photothermal agent and preparation method thereof, photothermal nanoparticle and preparation method thereof, insulating material and self-repairing method of insulating material 中国石油天然气股份有限公司 2024-06-14 CN claimed
CN-113355367-B Application of ketoacid reductase in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2024-03-26 CN claimed
CN-113355299-B Ketoacid reductase, gene, engineering bacterium and application in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2022-05-24 CN claimed
CN-113355367-A Application of ketoacid reductase in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2021-09-07 CN claimed
CN-113355299-A Ketoacid reductase, gene, engineering bacterium and application in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2021-09-07 CN claimed
CN-108410831-B Ketoacid reductase, gene, engineering bacterium and application in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2021-07-27 CN claimed
CN-108410831-A Ketoacid reductase, gene, engineering bacterium and application in synthesis of chiral aromatic 2-hydroxy acid 浙江工业大学 2018-08-17 CN claimed
EP-2485678-A1 COFERONS AND METHODS OF MAKING AND USING THEM Cornell University (US) 2012-08-15 EP claimed
WO-2011043817-A1 COFERONS AND METHODS OF MAKING AND USING THEM CORNELL UNIVERSITY (US) 2011-04-14 WO claimed
EP-4142874-B1 PYRIMIDIN-4(3H)-ONE DERIVATIVES AS TRPV4 ANTAGONISTS RAQUALIA PHARMA INC (JP) 2026-04-22 EP disclosed
US-12590064-B2 Substituted benzamides for inhibiting perk activity ELI LILLY AND COMPANY (US) 2026-03-31 US disclosed
EP-4688746-A1 CRYSTALLINE FORMS OF (R)-2-AMINO-5-(4-(2-(3,5-DIFLUOROPHENYL)-2-HYDROXYACETAMIDO)-2-METHYLPHENYL)-N-ISOPROPYLNICOTINAMIDE AND METHODS FOR USING THE SAME Hibercell, Inc. (US) 2026-02-11 EP disclosed
WO-2025242872-A1 1H-PYRAZOLO[4,3-D]PYRIMIDINE DERIVATIVES Apollo AP45 Limited (GB) 2025-11-27 WO disclosed
US-12473296-B2 Perk inhibiting compounds HIBERCELL, INC. (US) 2025-11-18 US disclosed
WO-1997002284-A1 NEW THROMBIN INHIBITORS, THEIR PREPARATION AND USE ASTRA AKTIEBOLAG (SE) 1997-01-23 WO disclosed
CN-1022913-C Herbicidal compositions containing new pyrrolidine derivative and its preparing method MITSUI TOATSU CHEMICALS (JP) 1993-12-01 CN disclosed
EP-0387869-B1 4-ETHYL-3-(SUBSTITUTED PHENYL)-1-(3-TRIFLUOROMETHYL-PHENYL)-2-PYRROLIDINONE DERIVATIVES, PROCESSES FOR THE PREPARATION AND USE THEREOF, HERBICIDAL COMPOSITIONS CONTAINING THEM MITSUI TOATSU CHEMICALS, Inc. (JP) 1993-07-21 EP disclosed
US-5131947-A 4-ETHYL-3-(SUBSTITUTED PHENYL)-1-(3-TRIFLUOROMETHYLPHENYL)-2-PYRROLIDINONE DERIVATIVES, HERBICIDAL COMPOSITIONS CONTAINING THEM AND USE THEREOF MITSUI TOATSU CHEMICALS INCORPORATED (JP) 1992-07-21 US disclosed
CN-1045581-A 4-ethyl-3-(substituted-phenyl)-1-(3-trifluoromethyl)-2-Pyrrolidone derivative, its preparation method contains the herbicidal composition of this derivative as activeconstituents MITSUI TOATSU CHEMICALS (JP) 1990-09-26 CN disclosed
EP-0387869-A2 4-Ethyl-3-(substituted phenyl)-1-(3-trifluoromethyl-phenyl)-2-pyrrolidinone derivatives, processes for the preparation and use thereof, herbicidal compositions containing them MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-09-19 EP 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-12473296-B2 Perk inhibiting compounds MAPK1, ERN1, MAP3K20 CES2 1592/4885CES1 282/4885LMNA 1117/4885
US-12590064-B2 Substituted benzamides for inhibiting perk activity EIF2AK3, EIF2AK1, EIF2AK4 CES2 675/4885CES1 1212/4885LMNA 1747/4885

“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.