SCHEMBL2587831

SCHEMBL2587831

O=C(O)Oc1ccc2c3cccc4cccc(c5ccc(OC(=O)O)c1c25)c43

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.39
TDP1 Q9NUW8 2/20 0.39
MAPT P10636 1/20 0.39
HSD17B10 Q99714 6/20 0.38
KMT2A Q03164 6/20 0.38
ALDH1A1 P00352 5/20 0.38
HPGD P15428 3/20 0.38
CYP1A2 P05177 3/20 0.38
POLB P06746 2/20 0.38
GLA P06280 1/20 0.38
CYP2D6 P10635 1/20 0.38
THRB P10828 1/20 0.38
GAA P10253 2/20 0.37
PGR P06401 1/20 0.37
PTGS1 P23219 1/20 0.37
MAPK1 P28482 1/20 0.37
NR4A1 P22736 1/20 0.36
NR4A2 P43354 1/20 0.36
NR4A3 Q92570 1/20 0.36
MEN1 O00255 3/20 0.36

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
SCHEMBL9350047 0.87 ALDH1A1 (0.48) KDM4ETDP1MAPTHSD17B10KMT2A
SCHEMBL297251 0.87 KDM4E (0.31) KDM4EALDH1A1GAARAB9A
SCHEMBL6238798 0.81 PKM (0.42) MAPTHSD17B10KMT2AALDH1A1CYP1A2
SCHEMBL9235830 0.81 KDM4E (0.42) KDM4EMAPTHSD17B10ALDH1A1HPGD
SCHEMBL28118916 0.81 ALDH1A1 (0.47) KDM4ETDP1MAPTHSD17B10KMT2A
SCHEMBL377249 0.81 KMT2A (0.40) KDM4ETDP1MAPTHSD17B10KMT2A
SCHEMBL1957981 0.81 KDM4E (0.46) KDM4ETDP1MAPTHSD17B10KMT2A
SCHEMBL5246333 0.80 KMT2A (0.50) KDM4ETDP1MAPTHSD17B10KMT2A
SCHEMBL8726041 0.79
SCHEMBL10594960 0.79 KMT2A (0.45) KDM4ETDP1MAPTHSD17B10KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0657436-A2 Process for the preparation of perylene-3,4-dicarboxylic acid derivatives, the compounds prepared according to this process and their use CIBA-GEIGY AG (CH) 1995-06-14 EP claimed
WO-2011134674-A1 IMPROVED LIGHT DIFFUSING COMPOSITION STYRON EUROPE GMBH (CH) 2011-11-03 WO disclosed
US-20100186801-A1 PHOTOVOLTAIC MODULES WITH IMPROVED QUANTUM EFFICIENCY BASF SE (DE) 2010-07-29 US disclosed
EP-2130233-A1 PHOTOVOLTAIC MODULES WITH IMPROVED QUANTUM EFFICIENCY BASF SE (DE) 2009-12-09 EP disclosed
EP-2008319-A2 LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF BASF SE (DE) 2008-12-31 EP disclosed
WO-2008113753-A1 METHOD FOR THE PRODUCTION OF RYLENE TETRACARBOXYLIC ACID DIIMIDES THE IMIDE NITROGENS OF WHICH CARRY HYDROGEN ATOMS AND THE USE THEREOF BASF SE (DE) 2008-09-25 WO disclosed
WO-2008110567-A1 PHOTOVOLTAIC MODULES WITH IMPROVED QUANTUM EFFICIENCY BASF SE (DE) 2008-09-18 WO disclosed
EP-1927141-A2 FLUORESCENT SOLAR CONVERSION CELLS BASED ON FLUORESCENT TERYLENE DYES BASF SE (DE) 2008-06-04 EP disclosed
WO-2007116001-A2 LIQUID CRYSTALLINE RYLENE TETRACARBOXYLIC ACID DERIVATIVES AND USE THEREOF BASF SE (DE) 2007-10-18 WO disclosed
EP-1812401-A1 METHOD FOR PRODUCING PERYLENE-3,4-DICARBOXYLIC ACID IMIDES BASF AKTIENGESELLSCHAFT (DE) 2007-08-01 EP disclosed
EP-1789415-A1 METHOD FOR PRODUCING QUATERRYLENE-3,4:13,14-TETRACARBOXY DIIMIDES BY DIRECT SYNTHESIS BASF AKTIENGESELLSCHAFT (DE) 2007-05-30 EP disclosed
WO-2007031446-A2 FLUORESCENT SOLAR CONVERSION CELLS BASED ON FLUORESCENT TERYLENE DYES BASF SE (DE) 2007-03-22 WO disclosed
WO-2006050860-A1 METHOD FOR PRODUCING PERYLENE-3,4-DICARBOXYLIC ACID IMIDES BASF AKTIENGESELLSCHAFT (DE) 2006-05-18 WO disclosed
WO-2006037539-A1 HALOGENATION OF RYLEN-CARBOXIMIDES WITH ELEMENTARY HALOGEN IN A TWO-PHASE MIXTURE COMPRISING AN ORGANIC SOLVENT AND WATER, WHEREIN FORMED HALOGEN HYDROCIDE IS CONTINUOUSLY REMOVABLE FROM THE ORGANIC SOLVENT BASF AKTIENGESELLSCHAFT (DE) 2006-04-13 WO disclosed
WO-2006021307-A1 METHOD FOR PRODUCING QUATERRYLENE-3,4:13,14-TETRACARBOXY DIIMIDES BY DIRECT SYNTHESIS BASF AKTIENGESELLSCHAFT (DE) 2006-03-02 WO disclosed
EP-1542975-A2 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES BASF AKTIENGESELLSCHAFT (DE) 2005-06-22 EP disclosed
WO-2004029028-A2 9-CYANO-SUBSTITUTED PERYLENE-3,4-DICARBOXYLIC ACID MONOIMIDES AS DYESTUFFS BASF AKTIENGESELLSCHAFT (DE) 2004-04-08 WO disclosed
EP-0657436-B1 Process for the preparation of perylene-3,4-dicarboxylic acid derivatives CIBA SC HOLDING AG (CH) 2001-12-12 EP disclosed
EP-0657436-A2 Process for the preparation of perylene-3,4-dicarboxylic acid derivatives, the compounds prepared according to this process and their use CIBA-GEIGY AG (CH) 1995-06-14 EP disclosed
EP-0657436-A2 Process for the preparation of perylene-3,4-dicarboxylic acid derivatives, the compounds prepared according to this process and their use CIBA-GEIGY AG (CH) 1995-06-14 EP disclosed