SCHEMBL9445972

SCHEMBL9445972

O=C(Oc1ccc(C(Cl)(Cl)Cl)cc1)Oc1ccc(C(Cl)(Cl)Cl)cc1

nearest known ligand 0.45

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.45
MEN1 O00255 2/20 0.45
ELANE P08246 8/20 0.41
KIF11 P52732 1/20 0.40
MAPT P10636 3/20 0.39
TDP1 Q9NUW8 2/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
TSHR P16473 1/20 0.39
HTT P42858 2/20 0.38
SMN1; SMN2 Q16637 2/20 0.38
RAB9A P51151 4/20 0.37
NPC1 O15118 1/20 0.36
LMNA P02545 1/20 0.35
NPSR1 Q6W5P4 2/20 0.35

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
SCHEMBL10489119 0.84 KIF11 (0.39) KMT2AMEN1ELANEKIF11MAPT
SCHEMBL9872014 0.79 KIF11 (0.43) ELANEKIF11MAPTTDP1L3MBTL1
SCHEMBL11444278 0.78 KMT2A (0.58) KMT2AMEN1ELANEMAPTHTT
SCHEMBL10339424 0.77 KMT2A (0.45) KMT2AMEN1ELANEMAPTTDP1
SCHEMBL47809 0.77 MAPT (0.61) KMT2AMEN1ELANEMAPTTDP1
SCHEMBL1720744 0.77 KIF11 (0.63) KMT2AMEN1KIF11
SCHEMBL1788787 0.74 ELANE (0.47) KMT2AMEN1ELANEKIF11MAPT
SCHEMBL236826 0.74 MAPT (0.53) KMT2AMEN1ELANEMAPTTDP1
SCHEMBL56865 0.73 KMT2A (0.50) KMT2AMEN1ELANEMAPTTSHR
SCHEMBL477017 0.72 MAPT (0.56) KMT2AMEN1ELANEMAPTTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-59170033-A None JP disclosed
JP-59001438-A None JP disclosed
JP-59001444-A None JP disclosed
EP-0506760-A4 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES 1993-03-10 EP disclosed
EP-0506760-A1 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES THE DOW CHEMICAL COMPANY (US) 1992-10-07 EP disclosed
WO-1991009003-A1 CATALYTIC METHOD TO PRODUCE HYDROXY SUBSTITUTED ARYLOPHENONES THE DOW CHEMICAL COMPANY (US) 1991-06-27 WO disclosed
US-5015778-A Catalytic method to produce hydroxy substituted arylophenones THE DOW CHEMICAL COMPANY (US) 1991-05-14 US disclosed
EP-0140050-B1 HEAT SENSITIVE RECORD MATERIAL HODOGAYA CHEMICAL CO., LTD. (JP) 1987-02-04 EP disclosed
US-4550329-A CONTAINING HYDROXY SUBSTITUTED BENZOPHENONE HODOGAYA CHEMICAL CO., LTD. (JP) 1985-10-29 US disclosed
EP-0140050-A1 Heat sensitive record material HODOGAYA CHEMICAL CO., LTD. (JP) 1985-05-08 EP disclosed
JP-S59170033-A PRODUCTION OF HYDROXYBENZOPHENONE COMPOUND HODOGAYA CHEM CO LTD 1984-09-26 JP disclosed
JP-S591444-A PREPARATION OF BIS(2-CHLORO-4-TRIFLUOROMETHYLPHENYL) CARBONATE HODOGAYA CHEM CO LTD 1984-01-06 JP disclosed
JP-S591438-A PREPARATION OF 4,4'-DIHYDROXYBENZOPHENONE HODOGAYA CHEM CO LTD 1984-01-06 JP disclosed