SCHEMBL1055858

SCHEMBL1055858

Cc1cc(C(N)=O)cc(C)c1CC(NC(=O)OC(C)(C)C)C(=O)O

nearest known ligand 0.49

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ACE P12821 1/20 0.49
ITGB3 P05106 2/20 0.46
ITGA2B P08514 2/20 0.46
ITGB1 P05556 1/20 0.46
ITGAV P06756 1/20 0.46
ITGB5 P18084 1/20 0.46
PPARA Q07869 9/20 0.45
PPARG P37231 8/20 0.45
PPARD Q03181 2/20 0.43
CTSS P25774 3/20 0.43
PTPN1 P18031 1/20 0.41
CTSL P07711 1/20 0.40
CTSB P07858 1/20 0.40
CTSK P43235 1/20 0.40
SCN9A Q15858 1/20 0.40
OPRM1 P35372 1/20 0.40
OPRD1 P41143 1/20 0.40
OPRK1 P41145 1/20 0.40

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
SCHEMBL1055857 1.00 ACE (0.49) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL13316851 0.90 CTSS (0.40) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL1056763 0.89 KLK5 (0.45) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL1056766 0.89 KLK5 (0.45) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL28385047 0.88 ACE (0.47) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL12600964 0.88 ACE (0.42) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL28102485 0.88 PPARA (0.43) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL28385045 0.88 ACE (0.47) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL19720147 0.88 PPARA (0.43) ACEITGB3ITGA2BITGB1ITGAV
SCHEMBL10604860 0.87 ACE (0.53) ACEITGB3ITGA2BITGB1ITGAV

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190177281-A1 PROCESS FOR THE PREPARATION OF 5-[[[(2S)-2-AMINO-3-[4-(AMINOCARBONYL)-2,6-DIMETHYLPHENYL]-1-OXOPROPYL] [(1S)-1-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]AMINO] METHYL-2-METHOXYBENZOIC ACID AND ITS POLYMORPHS THEREOF MSN LABORATORIES PRIVATE LIMITED (IN) 2019-06-13 US claimed
WO-2017191650-A1 PROCESS FOR THE PREPARATION OF 5-[[[(2S)-2-AMINO-3-[4-(AMINOCARBONYL)-2,6-DIMETHYLPHENYL]-1-OXOPROPYL][(1S)-1-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]AMINO]METHYL-2-METHOXYBENZOIC ACID AND ITS POLYMORPHS THEREOF MSN LABORATORIES PRIVATE LIMITED (IN) 2017-11-09 WO claimed
US-12637431-B2 Process for the preparation of 5-[[[(2S)-2-amino-3-[4-(aminocarbonyl)-2,6-dimethylphenyl]-1-oxopropyl] [(1S)-1-(4-phenyl-1H-imidazol-2-yl)ethyl]amino] methyl-2-methoxybenzoic acid and its polymorphs thereof MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2026-05-26 US disclosed
CN-110093382-B Chemical-biological preparation method of illicit-lin chiral intermediate 尚科生物医药(上海)有限公司 2023-08-29 CN disclosed
CN-110092735-B Preparation method of L-alanine derivative 尚科生物医药(上海)有限公司 2021-05-11 CN disclosed
CN-108026032-B Method for producing optically active 4-carbamoyl-2, 6-dimethylphenylalanine derivative 株式会社钟化 2020-09-29 CN disclosed
CN-106636241-B Method for preparing esmollin intermediate by enzyme method 尚科生物医药(上海)有限公司 2020-04-03 CN disclosed
CN-106636246-B Biological method for preparing (S) -1- (5-phenyl-1H-imidazole-2-yl) ethylamine 尚科生物医药(上海)有限公司 2020-03-24 CN disclosed
US-10479769-B2 Processes for the preparation of eluxadoline SUN PHARMACEUTICAL INDUSTRIES LIMITED (IN) 2019-11-19 US disclosed
US-20190248748-A1 PROCESSES FOR THE PREPARATION OF ELUXADOLINE SUN PHARMACEUTICAL INDUSTRIES LIMITED (IN) 2019-08-15 US disclosed
US-20190177281-A1 PROCESS FOR THE PREPARATION OF 5-[[[(2S)-2-AMINO-3-[4-(AMINOCARBONYL)-2,6-DIMETHYLPHENYL]-1-OXOPROPYL] [(1S)-1-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]AMINO] METHYL-2-METHOXYBENZOIC ACID AND ITS POLYMORPHS THEREOF MSN LABORATORIES PRIVATE LIMITED (IN) 2019-06-13 US disclosed
WO-2006099060-A2 PROCESS FOR THE PREPARATION OF OPIOID MODULATORS JANSSEN PHARMACEUTICA, N.V. (BE) 2006-09-21 WO disclosed
US-7041681-B2 Compounds as opioid receptor modulators JANSSEN PHARMACEUTICA N.V. (BE) 2006-05-09 US disclosed
US-20060030558-A1 Novel compounds as opioid receptor modulators BRESLIN HENRY J 2006-02-09 US disclosed
WO-2005090315-A1 NOVEL COMPOUNDS AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA, N. V. (BE) 2005-09-29 WO disclosed
US-20050203143-A1 use as pain relievers, gastrointestinal disorders such as inflammatory bowel disease; compounds are aminoacetamide derivatives substituted with an imidazole; 5-(([2-Amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino)-methyl)-2-methoxy-benzoic acid for example JANSSEN PHARMACEUTICA, N. V. (BE) 2005-09-15 US disclosed
US-20050187252-A1 2-Amino-3-(4-hydroxy-phenyl)-1-[2-(5-phenyl-oxazol-2-yl)-piperidin-1-yl]-propan-1-one; pain and gastrointestinal disorders BRESLIN HENRY J (US) 2005-08-25 US disclosed
EP-1499313-A2 HETEROCYCLIC DERIVATIVES AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA N.V. (BE) 2005-01-26 EP disclosed
US-20040010014-A1 Novel compounds as opioid receptor modulators JANSSEN PHARMACEUTICA, NV (BE) 2004-01-15 US disclosed
WO-2003092688-A2 HETEROCYCLIC DERIVATIVES AS OPIOID MODULATORS JANSSEN PHARMACEUTICA N.V. (BE) 2003-11-13 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 (8 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-20190248748-A1 PROCESSES FOR THE PREPARATION OF ELUXADOLINE CYP3A5, AVPR2, CYP3A4 ACE 377/4885ITGB3 2980/4885ITGA2B 2492/4885
US-20050203143-A1 use as pain relievers, gastrointestinal disorders such as inflammatory bowel disease; compounds are aminoacetamide derivatives substituted with an imidazole; 5-(([2-Amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino)-methyl)-2-methoxy-benzoic acid for example OPRK1, OPRM1, OPRL1 ACE 2301/4885ITGB3 3465/4885ITGA2B 2581/4885
US-20060030558-A1 Novel compounds as opioid receptor modulators OPRL1, OPRK1, OPRM1 ACE 3541/4885ITGB3 2971/4885ITGA2B 2460/4885
US-20190177281-A1 PROCESS FOR THE PREPARATION OF 5-[[[(2S)-2-AMINO-3-[4-(AMINOCARBONYL)-2,6-DIMETHYLPHENYL]-1-OXOPROPYL] [(1S)-1-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]AMINO] METHYL-2-METHOXYBENZOIC ACID AND ITS POLYMORPHS THEREOF CYP1B1, CYP1A1, CYP4B1 ACE 729/4885ITGB3 2190/4885ITGA2B 334/4885
US-20050187252-A1 2-Amino-3-(4-hydroxy-phenyl)-1-[2-(5-phenyl-oxazol-2-yl)-piperidin-1-yl]-propan-1-one; pain and gastrointestinal disorders OPRL1, OPRK1, OPRD1 ACE 3236/4885ITGB3 2093/4885ITGA2B 2193/4885
US-20040010014-A1 Novel compounds as opioid receptor modulators OPRL1, OPRK1, OPRM1 ACE 3541/4885ITGB3 2971/4885ITGA2B 2460/4885
US-12637431-B2 Process for the preparation of 5-[[[(2S)-2-amino-3-[4-(aminocarbonyl)-2,6-dimethylphenyl]-1-oxopropyl] [(1S)-1-(4-phenyl-1H-imidazol-2-yl)ethyl]amino] methyl-2-methoxybenzoic acid and its polymorphs thereof OPRD1, OPRK1, OPRM1 ACE 1707/4885ITGB3 1726/4885ITGA2B 1050/4885
US-10479769-B2 Processes for the preparation of eluxadoline CYP3A5, AVPR2, CYP3A4 ACE 377/4885ITGB3 2980/4885ITGA2B 2492/4885

“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.