SCHEMBL3540535

SCHEMBL3540535

O=C(O)Cc1ccccc1-c1ccc(Cl)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SUCNR1 Q9BXA5 4/20 0.56
PTGDR2 Q9Y5Y4 1/20 0.56
CYP2C19 P33261 1/20 0.54
FFAR4 Q5NUL3 2/20 0.53
FFAR1 O14842 1/20 0.53
KDM4E B2RXH2 1/20 0.51
DRD2 P14416 1/20 0.51
AKR1B1 P15121 1/20 0.50
GCG P01275 1/20 0.48
CXCL8 P10145 2/20 0.48
CYP2C9 P11712 1/20 0.48
CHRM1 P11229 1/20 0.48
KMT2A Q03164 1/20 0.47
PTGER1 P34995 1/20 0.47
PTGER4 P35408 1/20 0.47
PTGER3 P43115 1/20 0.47
PTGER2 P43116 1/20 0.47
PTGS2 P35354 1/20 0.47
SLC6A4 P31645 1/20 0.46
SLC6A3 Q01959 1/20 0.46

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
SCHEMBL5961842 0.87 PTGS1 (0.59) PTGDR2AKR1B1KMT2APTGER1PTGER4
SCHEMBL538512 0.87 KMT2A (0.60) PTGDR2FFAR4FFAR1AKR1B1KMT2A
SCHEMBL7598404 0.86 CYP2C19 (0.54) SUCNR1PTGDR2CYP2C19FFAR4FFAR1
Ammonia Solution, Strong SCHEMBL27926479 0.85 KMT2A (0.58) PTGDR2FFAR4FFAR1AKR1B1KMT2A
SCHEMBL8645744 0.85 PTGS1 (0.55) PTGDR2AKR1B1KMT2APTGER1PTGER4
SCHEMBL28594606 0.85 KMT2A (0.58) PTGDR2FFAR4FFAR1AKR1B1KMT2A
SCHEMBL27701716 0.85 KMT2A (0.58) PTGDR2FFAR4FFAR1KDM4EAKR1B1
Hydrochloric Acid SCHEMBL11895689 0.85 KMT2A (0.58) PTGDR2FFAR4FFAR1AKR1B1KMT2A
SCHEMBL29512995 0.85 KMT2A (0.58) PTGDR2FFAR4FFAR1AKR1B1KMT2A
SCHEMBL13802493 0.84 PTGER1 (0.49) SUCNR1PTGDR2AKR1B1CXCL8CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102746142-A Method for synthesis of 2-(2-(4-chlorphenyl)phenyl)acetic acid SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN claimed
CN-102746209-A A synthetic method for 3-(2-(4-chlorophenoxy)phenyl )-1-methyl-2,4-dione SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN claimed
CN-102791693-B Hepatitis c virus inhibitors BRISTOL-MYERS SQUIBB CO. (US) 2016-04-13 CN disclosed
WO-2015042405-A1 PH SWITCHABLE REAGENTS AND METHODS FOR THEIR USE IMPOSSIBLE FOODS INC. (US) 2015-03-26 WO disclosed
EP-1817031-B1 CASPASE-10 INHIBITORS FOR PREVENTION AND TREATMENT OF RETINOPATHY MERCK PATENT GMBH (DE) 2014-05-21 EP disclosed
CN-102746142-A Method for synthesis of 2-(2-(4-chlorphenyl)phenyl)acetic acid SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN disclosed
CN-102746142-A Method for synthesis of 2-(2-(4-chlorphenyl)phenyl)acetic acid SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN disclosed
CN-102746142-A Method for synthesis of 2-(2-(4-chlorphenyl)phenyl)acetic acid SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN disclosed
CN-102746209-A A synthetic method for 3-(2-(4-chlorophenoxy)phenyl )-1-methyl-2,4-dione SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN disclosed
CN-102746209-A A synthetic method for 3-(2-(4-chlorophenoxy)phenyl )-1-methyl-2,4-dione SHENGSHI TAIKE BIOLOG MEDICAL TECHNOLOGY SUZHOU CO LTD 2012-10-24 CN disclosed
US-20120142771-A1 BIPHENYLACETAMIDE DERIVATIVE DAINIPPON SUMITOMO PHARMA CO., LTD. (JP) 2012-06-07 US disclosed
US-7727990-B2 Melanocortin receptor-specific piperazine and keto-piperazine compounds PALATIN TECHNOLOGIES, INC. (US) 2010-06-01 US disclosed
US-20090155903-A1 PHARMACEUTICAL COMPOSITION AND METHOD MYRIAD GENETICS, INCORPORATED (US) 2009-06-18 US disclosed
US-20090155903-A1 PHARMACEUTICAL COMPOSITION AND METHOD MYRIAD GENETICS, INCORPORATED (US) 2009-06-18 US disclosed
US-20080255173-A1 Novel Specific Caspase-10 Inhibitors MERCK PATENT GESELLSCHAFT (DE) 2008-10-16 US disclosed
EP-1919479-A2 MELANOCORTIN RECEPTOR-SPECIFIC PIPERAZINE AND KETO-PIPERAZINE COMPOUNDS Palatin Technologies, Inc. (US) 2008-05-14 EP disclosed
EP-1817031-A1 NOVEL SPECIFIC CASPASE-10 INHIBITORS Merck Patent GmbH (DE) 2007-08-15 EP disclosed
WO-2007021991-A2 MELANOCORTIN RECEPTOR-SPECIFIC PIPERAZINE AND KETO-PIPERAZINE COMPOUNDS PALATIN TECHNOLOGIES, INC. (US) 2007-02-22 WO disclosed
US-20060287332-A1 Melanocortin Receptor-Specific Piperazine and Keto-Piperazine Compounds PALATIN TECHNOLOGIES, INC. (US) 2006-12-21 US disclosed
WO-2006058592-A1 NOVEL SPECIFIC CASPASE-10 INHIBITORS MERCK PATENT GMBH (DE) 2006-06-08 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 (4 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-20120142771-A1 BIPHENYLACETAMIDE DERIVATIVE HRH3, KCNH3, BRPF3 SUCNR1 1789/4885PTGDR2 1062/4885CYP2C19 240/4885
US-20080255173-A1 Novel Specific Caspase-10 Inhibitors CASP10, CASP1, CASP5 SUCNR1 3164/4885PTGDR2 3995/4885CYP2C19 2904/4885
US-20060287332-A1 Melanocortin Receptor-Specific Piperazine and Keto-Piperazine Compounds MC4R, MC5R, MC1R SUCNR1 606/4885PTGDR2 198/4885CYP2C19 2624/4885
US-20090155903-A1 PHARMACEUTICAL COMPOSITION AND METHOD APP, PSEN2, PSEN1 SUCNR1 4180/4885PTGDR2 2287/4885CYP2C19 390/4885

“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.