SCHEMBL8717639

SCHEMBL8717639

CCCN1c2cc(C)c(C)cc2C(C)(C)C12C=Nc1c(ccc3ncccc13)O2

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 4/20 0.43
MAPT P10636 4/20 0.43
THRB P10828 4/20 0.43
SMN1; SMN2 Q16637 3/20 0.43
ALOX12 P18054 2/20 0.43
L3MBTL1 Q9Y468 2/20 0.43
PKM P14618 1/20 0.43
ALDH1A1 P00352 2/20 0.39
HPGD P15428 2/20 0.39
HTT P42858 2/20 0.39
LMNA P02545 2/20 0.39
GAA P10253 1/20 0.39
POLB P06746 1/20 0.39
MAPK1 P28482 1/20 0.39
RECQL P46063 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
CYP3A4 P08684 1/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
BLM P54132 1/20 0.37

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
SCHEMBL14902888 0.90 MAPT (0.43) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL2397763 0.88 MAPT (0.54) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL5190280 0.86 MAPT (0.51) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL9115489 0.84 KDM4E (0.39) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL2401836 0.82 KDM4E (0.44) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL8717565 0.79 MAPT (0.62) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL7117468 0.76 MAPT (0.72) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL29493000 0.76 MAPT (0.72) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL10552518 0.75 MAPT (0.55) KDM4EMAPTTHRBSMN1; SMN2ALOX12
SCHEMBL9866811 0.75 KDM4E (0.43) KDM4EMAPTTHRBSMN1; SMN2ALOX12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2066714-B1 ABRASION AND/OR SCRATCH RESISTANT ARTICLE COMPRISING AN IMPACT RESISTANT PHOTOCHROMIC POLYURETHANE COATING, AND PROCESS OF PREPARATION THEREOF ESSILOR INT (FR) 2018-04-11 EP disclosed
US-20140209842-A1 SILICONE MATERIAL HAVING A PHOTOCHROMIC ADDITIVE LUXES BRAND, INCORPORATION (US) 2014-07-31 US disclosed
US-20130108858-A1 Methods for Making an Article Coated with a Photochromic Film and Use Thereof in Ophthalmological Optics Essilor International (Compagnie Generate d Optique (FR) 2013-05-02 US disclosed
US-20130108858-A1 Methods for Making an Article Coated with a Photochromic Film and Use Thereof in Ophthalmological Optics Essilor International (Compagnie Generate d Optique (FR) 2013-05-02 US disclosed
US-20100119802-A1 Abrasion and/or Scratch Resistant Article Comprising an Impact Resistant Photochromic Polyurethane Coating, and Process of Preparation Thereof FORD CHRISTY 2010-05-13 US disclosed
US-20100119802-A1 Abrasion and/or Scratch Resistant Article Comprising an Impact Resistant Photochromic Polyurethane Coating, and Process of Preparation Thereof FORD CHRISTY 2010-05-13 US disclosed
US-7662433-B2 impact resistant, abrasion and/or scratch resistant photochromic article comprising a substrate having two main faces, comprising: preparing a curable coating composition comprising at least one unblocked polyisocyanate terminated polyurethane pre-polymer, at least one polyol and a photochromic article ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2010-02-16 US disclosed
US-7662433-B2 impact resistant, abrasion and/or scratch resistant photochromic article comprising a substrate having two main faces, comprising: preparing a curable coating composition comprising at least one unblocked polyisocyanate terminated polyurethane pre-polymer, at least one polyol and a photochromic article ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2010-02-16 US disclosed
US-7608207-B2 Forming a hydrophilic polyurethane prepolymer with isocyanate end groups, mixing with a photochromic agent; adding water or a mixture of water and solvent, under agitation to form emulsion; adding chain extension agent ESSILOR INTERNATIONAL COMPAGNIE GENERALE D'OPTIQUE (FR) 2009-10-27 US disclosed
US-7608207-B2 Forming a hydrophilic polyurethane prepolymer with isocyanate end groups, mixing with a photochromic agent; adding water or a mixture of water and solvent, under agitation to form emulsion; adding chain extension agent ESSILOR INTERNATIONAL COMPAGNIE GENERALE D'OPTIQUE (FR) 2009-10-27 US disclosed
WO-2008031879-A1 ABRASION AND/OR SCRATCH RESISTANT ARTICLE COMPRISING AN IMPACT RESISTANT PHOTOCHROMIC POLYURETHANE COATING, AND PROCESS OF PREPARATION THEREOF ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2008-03-20 WO disclosed
US-20080067701-A1 Abrasion and/or Scratch Resistant Article Comprising an Impact Resistant Photochromic Polyurethane Coating, and Process of Preparation Thereof ESSILOR INTERNATIONAL (FR) 2008-03-20 US disclosed
US-20080067701-A1 Abrasion and/or Scratch Resistant Article Comprising an Impact Resistant Photochromic Polyurethane Coating, and Process of Preparation Thereof ESSILOR INTERNATIONAL (FR) 2008-03-20 US disclosed
WO-2007088312-A1 METHODS FOR MAKING AN ARTICLE COATED WITH A PHOTOCHROMIC FILM AND USE THEREOF IN OPHTHALMOLOGICAL OPTICS ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2007-08-09 WO disclosed
EP-0785936-A4 PHOTOCHROMIC NAPHTHOXAZINE COMPOUNDS PPG INDUSTRIES INC (US) 1998-07-08 EP disclosed
EP-0785936-A1 PHOTOCHROMIC NAPHTHOXAZINE COMPOUNDS PPG INDUSTRIES, INC. (US) 1997-07-30 EP disclosed
WO-1995016731-A1 COATING COMPOSITION AND ARTICLES HAVING A CURED COATING PPG INDUSTRIES, INC. (US) 1995-06-22 WO disclosed