SCHEMBL4711272

SCHEMBL4711272

Cc1ccc(C(=O)N(C(=O)c2ccc(C)cc2)C(=O)c2ccc(C)cc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.59
CES2 O00748 3/20 0.59
CES1 P23141 3/20 0.59
LMNA P02545 3/20 0.59
SMN1; SMN2 Q16637 3/20 0.56
HTT P42858 3/20 0.52
NPSR1 Q6W5P4 3/20 0.52
TDP1 Q9NUW8 3/20 0.52
KMT2A Q03164 3/20 0.52
PKM P14618 2/20 0.52
ATM Q13315 2/20 0.52
HPGD P15428 2/20 0.52
MEN1 O00255 2/20 0.52
NLRP1 Q9C000 1/20 0.52
GAA P10253 1/20 0.52
NTSR1 P30989 1/20 0.52
SRD5A2 P31213 1/20 0.50
HDAC1 Q13547 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
GSK3B P49841 1/20 0.48

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
SCHEMBL9368117 0.83 ALDH1A1 (0.46) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL469413 0.82 ALDH1A1 (0.61) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL11216329 0.82 ALDH1A1 (0.56) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL93592 0.80 ALDH1A1 (0.54) ALDH1A1CES2CES1LMNASMN1; SMN2
Hydrochloric Acid SCHEMBL29018542 0.80 ALDH1A1 (0.59) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL30280924 0.80 ALDH1A1 (0.54) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL8467615 0.80 ALDH1A1 (0.54) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL1441175 0.78 ALDH1A1 (0.52) ALDH1A1CES2CES1LMNASMN1; SMN2
Hydrochloric Acid SCHEMBL11274536 0.78 ALDH1A1 (0.52) ALDH1A1CES2CES1LMNASMN1; SMN2
SCHEMBL12084030 0.77 ALDH1A1 (0.50) ALDH1A1CES2CES1LMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1175130-B1 ELECTROLUMINESCENT ELEMENT NISSAN CHEMICAL IND LTD (JP) 2018-07-11 EP disclosed
EP-1248497-B1 ELECTROLUMINESCENCE ELEMENT NISSAN CHEMICAL IND LTD (JP) 2008-10-15 EP disclosed
EP-1156072-B1 AROMATIC AMINE DERIVATIVES, SOLUBLE CONDUCTIVE COMPOUND, AND ELECTROLUMINESCENT ELEMENT NISSAN CHEMICAL IND LTD (JP) 2007-01-03 EP disclosed
EP-1514866-B1 Process for producing cyanobenzoic acid derivatives SHOWA DENKO KK (JP) 2006-11-15 EP disclosed
EP-1514866-A1 Process for producing cyanobenzoic acid derivatives SHOWA DENKO KABUSHIKI KAISHA (JP) 2005-03-16 EP disclosed
EP-1508567-A2 Process for producing cyanobenzoic acid derivatives SHOWA DENKO KABUSHIKI KAISHA (JP) 2005-02-23 EP disclosed
US-6821648-B2 SALT OF AN ELECTRON ACCEPTING DOPANE AND POLYIMIDE OBTAINED FROM A DIAMINE COMPONENT CONTAINING AT LEAST 1 MOL % OF AN OLIGO-ANILINE UNIT-BEARING DIAMINOBENZENE DERIVATIVE AND A TETRACARBOXYLIC DIANHYDRIDE OR DERIVATIVE Kido, Junji (JP) 2004-11-23 US disclosed
US-6632544-B1 Antistatic coating; electromagnetic shields; durability Kido, Junji (JP) 2003-10-14 US disclosed
US-6632545-B1 Lower drive voltage preventing degradation Kido, Junji (JP) 2003-10-14 US disclosed
US-20020197494-A1 Electroluminescent element NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2002-12-26 US disclosed
EP-1248497-A1 ELECTROLUMINESCENCE ELEMENT Nissan Chemical Industries, Ltd. (JP) 2002-10-09 EP disclosed
US-6433211-B1 SELECTIVITY HYDRATION OF AROMATIC DINITRILES SHOWA DENKO KABUSHIKI KAISHA (JP) 2002-08-13 US disclosed
EP-1175130-A1 ELECTROLUMINESCENT ELEMENT Nissan Chemical Industries, Ltd. (JP) 2002-01-23 EP disclosed
EP-1156072-A1 AROMATIC AMINE DERIVATIVES, SOLUBLE CONDUCTIVE COMPOUND, AND ELECTROLUMINESCENT ELEMENT Nissan Chemical Industries, Ltd. (JP) 2001-11-21 EP disclosed
EP-0989115-A2 Process for producing cyanobenzoic acid derivatives Showa Denko Kabushiki Kaisha (JP) 2000-03-29 EP disclosed