SCHEMBL45259

SCHEMBL45259

CCCCCNc1cccc2c1C(=O)c1ccccc1C2=O

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 7/20 0.63
KMT2A Q03164 7/20 0.63
MAPT P10636 5/20 0.63
SMN1; SMN2 Q16637 4/20 0.63
L3MBTL1 Q9Y468 4/20 0.63
ALDH1A1 P00352 4/20 0.63
POLB P06746 4/20 0.63
MAPK1 P28482 3/20 0.63
HTT P42858 3/20 0.63
EGFR P00533 2/20 0.63
LMNA P02545 2/20 0.63
RECQL P46063 2/20 0.63
NPSR1 Q6W5P4 2/20 0.63
BLM P54132 2/20 0.63
RAD52 P43351 2/20 0.63
NSD2 O96028 2/20 0.57
FGB P02675 1/20 0.57
MMP14 P50281 1/20 0.57
TDP1 Q9NUW8 2/20 0.57
RAB9A P51151 2/20 0.57

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
SCHEMBL7853370 0.98 MEN1 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL7854850 0.98 MEN1 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL1898424 0.98 MEN1 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
Ammonia Solution, Strong SCHEMBL11423642 0.98 MEN1 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL13587207 0.98 MEN1 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL6291460 0.95 MEN1 (0.64) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL6055456 0.95 NSD2 (0.61) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL6372317 0.94 NSD2 (0.60) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL7855164 0.94 NSD2 (0.60) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1
SCHEMBL9906063 0.92 TERT (0.64) MEN1KMT2AMAPTSMN1; SMN2L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0069895-B1 PROCESS FOR CONDITIONING A PIGMENT Mobay Chemical Corporation (US) 1984-10-10 EP claimed
US-4062875-A FROM 2-ACYLAMINO-2'-CARBOXY-DIPHENYLMETHANE BAYER AKTIENGESELLSCHAFT (DT) 1977-12-13 US claimed
US-20130167308-A1 Method of Printing HERIOT-WATT UNIVERSITY (GB) 2013-07-04 US disclosed
WO-2011158007-A2 METHOD OF PRINTING HERIOT-WATT UNIVERSITY (GB) 2011-12-22 WO disclosed
EP-1106656-B1 PROCESS FOR PREPARING GREEN PIGMENT COMPOSITION CONTAINING NO HALOGEN TOYO INK MFG CO (JP) 2009-12-09 EP disclosed
CN-100554301-C Polyurethane articles, colorants and articles containing novel high toluene diisocyanate-stable blue colorants MILLIKEN CO (US) 2009-10-28 CN disclosed
CN-100350510-C Lead-free mixture used as radiation protection additive, preparation method and application thereof LANXESS DEUTSCHLAND GMBH (DE) 2007-11-21 CN disclosed
EP-1446443-B1 NOVEL POLYMERIC BLUE ANTHRAQUINONE-DERIVATIVE COLORANTS MILLIKEN & CO (US) 2007-11-14 EP disclosed
CN-1823109-A Polyurethane articles, colorants, and such articles comprising novel high toluene diisocyanate-stable blue colorants MILLIKEN CO (US) 2006-08-23 CN disclosed
CN-1748263-A Lead-free mixtures as radioprotective additives LANXESS DEUTSCHLAND GMBH (DE) 2006-03-15 CN disclosed
EP-1217045-B1 Halogen-free green pigment composition TOYO INK MFG CO (JP) 2005-07-27 EP disclosed
US-4992569-A Reacting substituted aminoanthraquinone with malodinitrile in inert solvent in presence of titanium tetrachloride and a tert iary-amine; textile dye CIBA-GEIGY CORPORATION (US) 1991-02-12 US disclosed
EP-0346280-A2 Dicyanobenzanthrone compounds CIBA-GEIGY AG (CH) 1989-12-13 EP disclosed
EP-0238443-A2 Dicyanobenzanthrone compounds CIBA-GEIGY AG (CH) 1987-09-23 EP disclosed
US-4493734-A Conditioning of crude pigment in a salt free corn syrup based medium MOBAY CHEMICAL CORPORATION (US) 1985-01-15 US disclosed
US-4435492-A UNSATURATED, NONIONIC CHARGE TRANSPORT MATERIAL HITACHI, LTD. (JP) 1984-03-06 US disclosed
US-4432796-A Process for the conditioning of an organic pigment MOBAY CHEMICAL CORPORATION (US) 1984-02-21 US disclosed
US-4163747-A Process for the preparation of 1-alkylamino-anthraquinones BAYER AKTIENGESELLSCHAFT (DE) 1979-08-07 US disclosed
US-4062875-A FROM 2-ACYLAMINO-2'-CARBOXY-DIPHENYLMETHANE BAYER AKTIENGESELLSCHAFT (DT) 1977-12-13 US disclosed
US-4062875-A FROM 2-ACYLAMINO-2'-CARBOXY-DIPHENYLMETHANE BAYER AKTIENGESELLSCHAFT (DT) 1977-12-13 US disclosed