SCHEMBL7901094

SCHEMBL7901094

Cc1ccc(N(c2ccc(C)cc2)c2ccc(CCc3ccc(NC(=O)c4cc5ccc6c7ccccc7[nH]c6c5cc4O)cc3)cc2)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 7/20 0.65
▸ MEN1 O00255 5/20 0.65
▸ MAPT P10636 3/20 0.65
▸ KDM4E B2RXH2 2/20 0.65
▸ CACNA1B Q00975 1/20 0.65
▸ APBA1 Q02410 1/20 0.65
▸ MPL P40238 4/20 0.53
▸ POLB P06746 3/20 0.47
▸ NPC1 O15118 3/20 0.47
▸ RAB9A P51151 3/20 0.47
▸ GAA P10253 1/20 0.44
▸ ALOX15 P16050 3/20 0.43
▸ PARP14 Q460N5 1/20 0.42
▸ ADORA3 P0DMS8 1/20 0.41
▸ PLG P00747 2/20 0.41
▸ KLK1 P06870 2/20 0.41
▸ KLK6 Q92876 2/20 0.41
▸ NTRK1 P04629 1/20 0.41
▸ ALPL P05186 1/20 0.40
▸ ALPI P09923 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
SCHEMBL10987424 0.89 KMT2A (0.79) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL10989850 0.86 KMT2A (0.75) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL7899348 0.86 KMT2A (0.61) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL175806 0.81 KMT2A (0.78) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL9354492 0.80 KMT2A (0.70) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL29405509 0.79 MEN1 (1.00) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL5820002 0.79 MEN1 (1.00) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL10983073 0.77 MEN1 (0.63) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL10980076 0.77 KMT2A (0.63) KMT2AMEN1MAPTKDM4ECACNA1B
SCHEMBL9358087 0.77 KMT2A (0.66) KMT2AMEN1MAPTKDM4ECACNA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6271356-B1 TRISAZO COMPOUND WITH BENZO(A)CARBAZOLE RINGS EMPLOYED AS THE COMPOUND HAVING A CHARGE GENERATING MOIETY AND A CHARGE TRANSPORTING MOIETY IN THE MOLECULE THEREOF FOR USE IN THE ELECTROPHOTOGRAPHIC PHOTOCONDUCTOR. RICOH COMPANY, LTD. (JP) 2001-08-07 — — US disclosed
US-6184362-B1 Electrophotographic photoconductor, azo compounds for use in the same, and intermediates for producing the azo compounds RICOH COMPANY, LTD. (JP) 2001-02-06 — — US disclosed
US-6103435-A A COMPOUND HAVING AN AZO CHARGE GENERATING MOIETY AND A TRIARYLAMINO CHARGE TRANSPORTING MOIETY IN THE MOLECULE RICOH COMPANY, LTD. (JP) 2000-08-15 — — US disclosed
US-5981124-A PHOTOCONDUCTIVE LAYER COMPRISES A COMPOUND CONTAINING AN AZO CHARGE GENERATING GROUP, A TRAIARYLAMINO CHARGE TRANSPORTING GROUP AND A BIVALENT COUPLER RICOH COMPANY, LTD. (JP) 1999-11-09 — — US disclosed
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