SCHEMBL1505378

SCHEMBL1505378

Cc1cc(C(N)=O)cc(C)c1Br

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 3/20 0.44
▸ APOBEC3A P31941 1/20 0.44
▸ HTT P42858 1/20 0.44
▸ APOBEC3G Q9HC16 1/20 0.44
▸ PARP1 P09874 6/20 0.43
▸ CYP3A4 P08684 2/20 0.39
▸ SMN1; SMN2 Q16637 2/20 0.39
▸ NCOA1 Q15788 1/20 0.39
▸ NCOA3 Q9Y6Q9 1/20 0.39
▸ MAPT P10636 2/20 0.38
▸ POLB P06746 1/20 0.37
▸ CYP2C19 P33261 1/20 0.37
▸ RECQL P46063 1/20 0.37
▸ BLM P54132 1/20 0.37
▸ PMP22 Q01453 1/20 0.37
▸ HSD17B10 Q99714 1/20 0.37
▸ TDP1 Q9NUW8 1/20 0.37
▸ L3MBTL1 Q9Y468 1/20 0.37
▸ ALDH1A1 P00352 2/20 0.37
▸ MEN1 O00255 1/20 0.37

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
SCHEMBL29710362 0.80 HTT (0.49) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL19358016 0.80 HTT (0.49) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL18471225 0.80 SMN1; SMN2 (0.49) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL10831613 0.80 PARP1 (0.46) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL1004660 0.78 PARP1 (0.50) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL12983073 0.78 CA5A (0.48) SMN1; SMN2MAPTTDP1L3MBTL1ALDH1A1
SCHEMBL1397262 0.78 POLB (0.50) TSHRAPOBEC3AHTTAPOBEC3GPARP1
SCHEMBL850504 0.78 TPMT (0.54) TSHRSMN1; SMN2MAPTHSD17B10TDP1
SCHEMBL3220166 0.78 CA1 (0.48) TSHRPARP1CYP3A4SMN1; SMN2MAPT
SCHEMBL1002938 0.76 CYP3A4 (0.48) TSHRAPOBEC3AHTTAPOBEC3GPARP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
EP-3068768-B1 ANTIDIABETIC TRICYCLIC COMPOUNDS MERCK SHARP & DOHME (US) 2019-07-31 — — EP disclosed
EP-3068768-B1 ANTIDIABETIC TRICYCLIC COMPOUNDS MERCK SHARP & DOHME (US) 2019-07-31 — — EP disclosed
EP-3112352-B1 OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2018-11-21 — — EP disclosed
US-20180325870-A1 NOVEL COMPOUNDS AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA, N.V. (BE) 2018-11-15 — — US disclosed
US-9700542-B2 Compounds as opioid receptor modulators JANSSEN PHARMACEUTICA NV (BE) 2017-07-11 — — US disclosed
US-9700542-B2 Compounds as opioid receptor modulators JANSSEN PHARMACEUTICA NV (BE) 2017-07-11 — — US disclosed
US-9700542-B2 Compounds as opioid receptor modulators JANSSEN PHARMACEUTICA NV (BE) 2017-07-11 — — US disclosed
EP-3112352-A1 OPIOID RECEPTOR MODULATORS Janssen Pharmaceutica NV (BE) 2017-01-04 — — EP disclosed
US-9487517-B2 Spiroimidazolone derivative CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-11-08 — — US disclosed
US-20080096888-A1 pain relievers; gastrointestinal disorders; inflammatory bowel disease, diarrhea, motility disorders; 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 JANSSEN PHARMACEUTICA, N.V. (BE) 2008-04-24 — — US disclosed
EP-1863764-A1 PROCESS FOR THE PREPARATION OF OPIOID MODULATORS Janssen Pharmaceutica, N.V. (BE) 2007-12-12 — — EP disclosed
EP-1858850-A2 PROCESS FOR THE PREPARATION OF OPIOID MODULATORS JANSSEN PHARMACEUTICA N.V. (BE) 2007-11-28 — — EP disclosed
EP-1725537-A1 NOVEL COMPOUNDS AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA N.V. (BE) 2006-11-29 — — EP disclosed
WO-2006099060-A2 PROCESS FOR THE PREPARATION OF OPIOID MODULATORS JANSSEN PHARMACEUTICA, N.V. (BE) 2006-09-21 — — WO disclosed
WO-2006098982-A1 PROCESS FOR THE PREPARATION OF OPIOID MODULATORS JANSSEN PHARMACEUTICA, N.V. (BE) 2006-09-21 — — WO disclosed
US-20060211861-A1 Process for the preparation of opioid modulators JANSSEN PHARMACEUTICA N.V. (BE) 2006-09-21 — — US disclosed
US-20060211863-A1 Process for the preparation of opioid modulators JANSSEN PHARMACEUTICA N.V. (BE) 2006-09-21 — — 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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-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 TSHR 2171/4885APOBEC3A 4607/4885HTT 3825/4885
US-20060211861-A1 Process for the preparation of opioid modulators OPRM1, OPRK1, OPRL1 TSHR 1255/4885APOBEC3A 4053/4885HTT 2747/4885
US-20080096888-A1 pain relievers; gastrointestinal disorders; inflammatory bowel disease, diarrhea, motility disorders; 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 OPRK1, OPRM1, OPRL1 TSHR 1793/4885APOBEC3A 4489/4885HTT 3902/4885
US-20180325870-A1 NOVEL COMPOUNDS AS OPIOID RECEPTOR MODULATORS OPRM1, OPRK1, OPRL1 TSHR 410/4885APOBEC3A 4783/4885HTT 3569/4885
US-20060211863-A1 Process for the preparation of opioid modulators OPRM1, OPRK1, OPRL1 TSHR 1255/4885APOBEC3A 4053/4885HTT 2747/4885

“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.

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