SCHEMBL2706993

SCHEMBL2706993

COC(=O)C(=O)c1ccc(Cl)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 4/20 0.62
CES1 P23141 4/20 0.62
HPGD P15428 1/20 0.52
ALOX15 P16050 1/20 0.48
TSHR P16473 1/20 0.48
ALDH1A1 P00352 2/20 0.47
MAPT P10636 2/20 0.47
LMNA P02545 2/20 0.47
KDM4E B2RXH2 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
CA1 P00915 2/20 0.46
CA2 P00918 2/20 0.46
CYP11B1 P15538 2/20 0.46
CYP11B2 P19099 2/20 0.46
PTGS2 P35354 2/20 0.45
MEN1 O00255 1/20 0.44
NPC1 O15118 1/20 0.44
HTT P42858 1/20 0.44
RAB9A P51151 1/20 0.44
KMT2A Q03164 1/20 0.44

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
SCHEMBL22407070 0.91 HPGD (0.53) CES2CES1HPGDTSHRALDH1A1
SCHEMBL9045102 0.86 L3MBTL1 (0.58) CES2CES1HPGDALDH1A1MAPT
SCHEMBL28452278 0.83 CES2 (0.45) CES2CES1HPGDTSHRALDH1A1
SCHEMBL28450705 0.80 MAPT (0.52) CES2CES1HPGDALDH1A1MAPT
SCHEMBL2440560 0.80 CA1 (0.61) HPGDTSHRALDH1A1MAPTKDM4E
SCHEMBL4587615 0.80 CA1 (0.56) CES2CES1HPGDALOX15TSHR
SCHEMBL3757531 0.80 CES2 (0.65) CES2CES1HPGDALDH1A1MAPT
SCHEMBL2601260 0.80 CA1 (0.61) CES2CES1HPGDTSHRALDH1A1
SCHEMBL8672089 0.79 CES2 (0.58) CES2CES1HPGDALOX15TSHR
SCHEMBL4735784 0.79 CYP2C9 (0.47) CES2CES1HPGDALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114685298-B Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2023-10-24 CN claimed
CN-114685298-A Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2022-07-01 CN claimed
US-20260070874-A1 BENZOYLFORMIC ACID AMIDE DERIVATIVE KJ CHEMICALS CORPORATION (JP) 2026-03-12 US disclosed
EP-4610249-A1 BENZOYLFORMIC ACID AMIDE DERIVATIVE KJ Chemicals Corporation (JP) 2025-09-03 EP disclosed
CN-114685298-B Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2023-10-24 CN disclosed
CN-114685298-B Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2023-10-24 CN disclosed
CN-114761004-A Process for the preparation of 2- (4-chlorophenyl) -N- ((2- (2, 6-dioxopiperidin-3-yl) -1-oxoisoindolin-5-yl) methyl) -2, 2-difluoroacetamide 细胞基因公司 2022-07-15 CN disclosed
US-20220213056-A1 PROCESSES FOR PREPARING 2-(4-CHLOROPHENYL)-N-((2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLIN-5-YL)METHYL)-2,2-DIFLUOROACETAMIDE CELGENE CORP (US) 2022-07-07 US disclosed
US-20220213056-A1 PROCESSES FOR PREPARING 2-(4-CHLOROPHENYL)-N-((2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLIN-5-YL)METHYL)-2,2-DIFLUOROACETAMIDE CELGENE CORP (US) 2022-07-07 US disclosed
CN-114685298-A Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2022-07-01 CN disclosed
CN-114685298-A Method for synthesizing baclofen based on photocatalytic migration strategy 兰州大学 2022-07-01 CN disclosed
WO-1995023139-A1 OPTICALLY PURE 4-ARYL-2-HYDROXYTETRONIC ACIDS THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1995-08-31 WO disclosed
EP-0403812-B1 Diketopiperazine derivatives, their preparation and their use as dyestuff BAYER AG (DE) 1995-07-12 EP disclosed
US-5399721-A Anticoagulant; prepared from aldehyde THE OHIO STATE UNIVERSITY RESEARCH FOUNDATION (US) 1995-03-21 US disclosed
EP-0602009-A2 Heterocyclic compounds BAYER AG (DE) 1994-06-15 EP disclosed
EP-0552631-A1 Alpha-aryl-alpha-hydroxy-beta-imidazolinylpropionamides BAYER AG (DE) 1993-07-28 EP disclosed
US-5164496-A Coloring plastics, paints, inks BAYER AKTIENGESELLSCHAFT (DE) 1992-11-17 US disclosed
EP-0403812-A2 Diketopiperazine derivatives, their preparation and their use as dyestuff BAYER AG (DE) 1990-12-27 EP disclosed
EP-0386940-A1 6-Beta-(alpha-etherified oxymino)-acyl amino penicillins BEECHAM GROUP PLC (GB) 1990-09-12 EP disclosed
EP-0217214-A1 2,4-dioxopyrrolo(2,3-c)pyrroles BAYER AG (DE) 1987-04-08 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-20220213056-A1 PROCESSES FOR PREPARING 2-(4-CHLOROPHENYL)-N-((2-(2,6-DIOXOPIPERIDIN-3-YL)-1-OXOISOINDOLIN-5-YL)METHYL)-2,2-DIFLUOROACETAMIDE DCPS, DNMT1, DPYD CES2 1359/4885CES1 2560/4885HPGD 2226/4885
US-20260070874-A1 BENZOYLFORMIC ACID AMIDE DERIVATIVE CRYAA, BCAT1, BRCA1 CES2 1111/4885CES1 945/4885HPGD 2349/4885

“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.