SCHEMBL3781228

SCHEMBL3781228

NC(=O)c1cc(N)cc(-c2ccccc2)c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DHODH Q02127 6/20 0.68
MKNK1 Q9BUB5 2/20 0.50
CYP3A4 P08684 2/20 0.50
MKNK2 Q9HBH9 1/20 0.50
POLB P06746 1/20 0.50
PARP1 P09874 1/20 0.50
MAPT P10636 1/20 0.50
TSHR P16473 1/20 0.50
CYP2C19 P33261 1/20 0.50
RECQL P46063 1/20 0.50
BLM P54132 1/20 0.50
PMP22 Q01453 1/20 0.50
HSD17B10 Q99714 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
IKBKB O14920 5/20 0.49
MAOA P21397 1/20 0.47
CHEK2 O96017 1/20 0.46
KMO O15229 1/20 0.46
CHUK O15111 2/20 0.45

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
SCHEMBL186316 0.88 DHODH (0.85) DHODHMKNK1CYP3A4MKNK2POLB
SCHEMBL3791008 0.87 DHODH (0.57) DHODHMKNK2PARP1MAPTMAOA
SCHEMBL2726729 0.86 DHODH (0.65) DHODHMAOAKMOPBRM1
SCHEMBL3786549 0.86 DHODH (0.55) DHODHMKNK1CYP3A4MKNK2TDP1
SCHEMBL1516770 0.83 DHODH (0.71) DHODHMKNK1CYP3A4MKNK2POLB
SCHEMBL3787106 0.83 MAPT (0.57) DHODHMAPTMAOAKMOPBRM1
SCHEMBL24587795 0.81 DHODH (0.54) DHODHPARP1
SCHEMBL18120862 0.81 DHODH (1.00) DHODHMKNK1CYP3A4MKNK2POLB
SCHEMBL30387022 0.81 DHODH (1.00) DHODHMKNK1CYP3A4MKNK2POLB
SCHEMBL6833627 0.80 DHODH (0.45) DHODHMAPTL3MBTL1MAOAKMO

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12042543-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 NORTHWESTERN UNIVERSITY (US) 2024-07-23 US disclosed
US-12042543-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 NORTHWESTERN UNIVERSITY (US) 2024-07-23 US disclosed
US-12042543-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 NORTHWESTERN UNIVERSITY (US) 2024-07-23 US disclosed
US-20230346953-A1 SUBSTITUTED 3-AMINO-5-PHENYLBENZAMIDE COMPOUNDS AS COVALENT INHIBITORS OF ENHANCER ZESTE HOMOLOG 2 (EZH2) AND PROTEOLYSIS-TARGETING CHIMERIC DERIVATIVES THEREOF (PROTACS) THAT INDUCE DEGRADATION OF EZH2 UNITED STATES GOVERNMENT 2023-11-02 US disclosed
US-20230346953-A1 SUBSTITUTED 3-AMINO-5-PHENYLBENZAMIDE COMPOUNDS AS COVALENT INHIBITORS OF ENHANCER ZESTE HOMOLOG 2 (EZH2) AND PROTEOLYSIS-TARGETING CHIMERIC DERIVATIVES THEREOF (PROTACS) THAT INDUCE DEGRADATION OF EZH2 UNITED STATES GOVERNMENT 2023-11-02 US disclosed
US-20100087680-A1 METHOD FOR PRODUCING BIARYL COMPOUND SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2010-04-08 US disclosed
EP-1914221-A1 PROCESS FOR PRODUCING BIARYL COMPOUND Sumitomo Chemical Company, Limited (JP) 2008-04-23 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 (3 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-12042543-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 EZH2, BAZ2A, BAZ2B DHODH 4037/4885MKNK1 873/4885CYP3A4 2705/4885
US-20100087680-A1 METHOD FOR PRODUCING BIARYL COMPOUND NISCH, BLVRB, BBOX1 DHODH 869/4885MKNK1 3527/4885CYP3A4 177/4885
US-20230346953-A1 SUBSTITUTED 3-AMINO-5-PHENYLBENZAMIDE COMPOUNDS AS COVALENT INHIBITORS OF ENHANCER ZESTE HOMOLOG 2 (EZH2) AND PROTEOLYSIS-TARGETING CHIMERIC DERIVATIVES THEREOF (PROTACS) THAT INDUCE DEGRADATION OF EZH2 EZH2, BAZ2A, BAZ2B DHODH 4037/4885MKNK1 873/4885CYP3A4 2705/4885

“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.