SCHEMBL2906103

SCHEMBL2906103

CC(=O)OC(C(=O)O)c1ccccc1Nc1c(Cl)cccc1Cl

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CXCL8 P10145 8/20 0.65
PTGS2 P35354 5/20 0.47
TTR P02766 3/20 0.47
PTGS1 P23219 2/20 0.47
AKR1B10 O60218 1/20 0.47
UGT1A9 O60656 1/20 0.47
TRPA1 O75762 1/20 0.47
ABCB11 O95342 1/20 0.47
MT-CO2 P00403 1/20 0.47
ALB P02768 1/20 0.47
UGT1A6 P19224 1/20 0.47
UGT1A1 P22309 1/20 0.47
CXCR1 P25024 1/20 0.47
ADRA1A P35348 1/20 0.47
AGTR2 P50052 1/20 0.47
NR1I3 Q14994 1/20 0.47
SLC22A6 Q4U2R8 1/20 0.47
NR1H4 Q96RI1 1/20 0.47
UGT1A7 Q9HAW7 1/20 0.47
UGT1A10 Q9HAW8 1/20 0.47

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
SCHEMBL10952727 0.85 CXCL8 (0.53) CXCL8PTGS2TTRPTGS1AKR1B10
SCHEMBL6256539 0.84 CXCL8 (0.53) CXCL8PTGS2TTRPTGS1AKR1B10
SCHEMBL10651614 0.84 CXCL8 (0.64) CXCL8PTGS2TTRPTGS1AKR1B10
SCHEMBL11093807 0.82 CXCL8 (0.58) CXCL8PTGS2TTRPTGS1AKR1B10
SCHEMBL29845650 0.81 TSHR (0.48) CXCL8LMNAKMT2ACYP3A4TSHR
SCHEMBL8069967 0.81 TSHR (0.48) CXCL8LMNAKMT2ACYP3A4TSHR
SCHEMBL19451943 0.81 TSHR (0.48) CXCL8LMNAKMT2ACYP3A4TSHR
SCHEMBL29973372 0.81 TSHR (0.48) CXCL8LMNAKMT2ACYP3A4TSHR
SCHEMBL3137707 0.79 CXCL8 (1.00) CXCL8PTGS2TTRPTGS1AKR1B10
SCHEMBL12129515 0.79 CXCL8 (1.00) CXCL8PTGS2TTRPTGS1AKR1B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005073163-A1 A PROCESS FOR THE PREPARATION OF [2-(2,6-DICHLORO ANILINO) PHENYL] ACETOXY ACETIC ACID J.B.CHEMICALS & PHARMACEUTICALS LTD. (IN) 2005-08-11 WO claimed
US-4548952-A ANTINFLAMMATORY, ANALGESIC AGENTS PRODES, S.A. (ES) 1985-10-22 US claimed
JP-63063647-A None JP disclosed
EP-3838270-B1 SYNERGISTIC PHARMACEUTICAL COMPOSITION COMPRISING ACECLOFENAC AND BETAMETHASONE FOR THE TREATMENT OF PAIN IN LOCALISED FORMS OF RHEUMATIC ILLNESSES AMEZCUA AMEZCUA FEDERICO (MX) 2024-10-09 EP disclosed
US-20210228598-A1 SYNERGISTIC PHARMACEUTICAL COMPOSITION COMPRISING ACECLOFENAC AND BETAMETHASONE FOR THE TREATMENT OF PAIN IN LOCALISED FORMS OF RHEUMATIC ILLNESSES Amezcua Amezcua, Federico (MX) 2021-07-29 US disclosed
EP-3838270-A2 SYNERGISTIC PHARMACEUTICAL COMPOSITION COMPRISING ACECLOFENAC AND BETAMETHASONE FOR THE TREATMENT OF PAIN IN LOCALISED FORMS OF RHEUMATIC ILLNESSES Amézcua Amézcua, Federico (MX) 2021-06-23 EP disclosed
EP-2393486-A1 ACECLOFENAC-CONTAINING CONTROLLED-RELEASE ORAL DRUG PREPARATIONS AND THEIR MANUFACTURING PROCESS Korea United Pharm, Inc. (KR) 2011-12-14 EP disclosed
WO-2010090371-A1 ACECLOFENAC-CONTAINING CONTROLLED-RELEASE ORAL DRUG PREPARATIONS AND THEIR MANUFACTURING PROCESS KOREA UNITED PHARM, INC (KR) 2010-08-12 WO disclosed
EP-1814517-B1 NONAQUEOUS LIQUID PARENTERAL ACECLOFENAC FORMULATION VENUS REMEDIES LTD (IN) 2010-08-11 EP disclosed
WO-2010008135-A1 ORAL SOFT CAPSULE OF ACECLOFENAC HAVING IMPROVED STABILITY KOREA UNITED PHARM, INC (KR) 2010-01-21 WO disclosed
US-20090156670-A1 NONAQUEOUS LIQUID PARENTERAL ACECLOFENAC FORMULATION VENUS REMEDIES LIMITED (IN) 2009-06-18 US disclosed
WO-2005073163-A1 A PROCESS FOR THE PREPARATION OF [2-(2,6-DICHLORO ANILINO) PHENYL] ACETOXY ACETIC ACID J.B.CHEMICALS & PHARMACEUTICALS LTD. (IN) 2005-08-11 WO disclosed
WO-2005073163-A1 A PROCESS FOR THE PREPARATION OF [2-(2,6-DICHLORO ANILINO) PHENYL] ACETOXY ACETIC ACID J.B.CHEMICALS & PHARMACEUTICALS LTD. (IN) 2005-08-11 WO disclosed
US-6310099-B1 5-METHYL OR ETHYL-2-(2-'CHLORO OR FLUORO OR TRIFLUROMETHYL-6'FLUORO OR CHLOROANILINO) PHENYLACETIC ACID OR SALT IS USED AS COX-2 SELECTIVE CYCLOOXYGENASE INHIBITOR NOVARTIS AG (CH) 2001-10-30 US disclosed
US-5844696-A Nitric esters from derivatives of 2-(2,6-dihalophenylamino) phenylacetoxyacetic acid and their preparation process PRODES, S.A. (ES) 1998-12-01 US disclosed
EP-0738706-B1 Nitric esters of 2-(2,6-dihalophenylamino) phenylacetoxyacetic acid derivatives and their preparation process PRODES SA (ES) 1998-10-07 EP disclosed
EP-0738706-A1 Nitric esters of 2-(2,6-dihalophenylamino) phenylacetoxyacetic acid derivatives and their preparation process PRODES, S.A. (ES) 1996-10-23 EP disclosed
JP-S6363647-A NOVEL 2-((2,6-DICHLOROPHENYL)AMINO)PHENYLACETOXYACETIC ACID DERIVATIVE UJI SEIYAKU KK 1988-03-22 JP disclosed
EP-0119932-B1 NEW 2-((2,6-DICHLOROPHENYL)AMINE)PHENYLACETOXYACETYL DERIVATIVES, THE PROCESS FOR PREPARING THE SAME AND THEIR USE IN THERAPEUTICS PRODES S.A. (ES) 1987-05-13 EP disclosed
US-4548952-A ANTINFLAMMATORY, ANALGESIC AGENTS PRODES, S.A. (ES) 1985-10-22 US 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 (1 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-20210228598-A1 SYNERGISTIC PHARMACEUTICAL COMPOSITION COMPRISING ACECLOFENAC AND BETAMETHASONE FOR THE TREATMENT OF PAIN IN LOCALISED FORMS OF RHEUMATIC ILLNESSES ACE, ACE2, TSLP CXCL8 1393/4885PTGS2 791/4885TTR 176/4885

“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.