SCHEMBL2801293

SCHEMBL2801293

Oc1ccc(-n2nc3ccc(Br)cc3n2)c(O)c1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 4/20 0.37
RAB9A P51151 4/20 0.37
LMNA P02545 2/20 0.37
PDK1 Q15118 2/20 0.36
PDK2 Q15119 2/20 0.36
PDK3 Q15120 2/20 0.36
PDK4 Q16654 2/20 0.36
MEN1 O00255 6/20 0.35
KMT2A Q03164 6/20 0.35
MAPT P10636 2/20 0.35
ALDH1A1 P00352 1/20 0.35
GAA P10253 2/20 0.35
KDM4E B2RXH2 1/20 0.35
HPGD P15428 1/20 0.35
HTT P42858 1/20 0.35
HKDC1 Q2TB90 1/20 0.35
KDM4C Q9H3R0 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
USP2 O75604 1/20 0.34

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
SCHEMBL17201891 0.88 NPC1 (0.42) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL7785471 0.84 MEN1 (0.51) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL28556638 0.83 NPC1 (0.40) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL26578933 0.81 NPC1 (0.51) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL45835 0.81 NPC1 (0.54) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL5834566 0.81 ALOX5 (0.41) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL9010899 0.81 NPC1 (0.55) NPC1RAB9ALMNAPDK1PDK2
SCHEMBL30383298 0.81 MAPT (0.41) NPC1RAB9ALMNAMEN1KMT2A
SCHEMBL7783973 0.81 AMY1A (0.42) NPC1RAB9ALMNAPDK1PDK2
SCHEMBL29602456 0.81 AMY1A (0.42) NPC1RAB9ALMNAPDK1PDK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3161528-B1 COMPOSITION FOR THE MANUFACTURE OF AN OPHTALMIC LENS COMPRISING AN UV-ABSORBER AND AN ANTI-YELLOWING ADDITIVE ESSILOR INT (FR) 2020-03-04 EP disclosed
US-10370520-B2 Composition for the manufacture of an ophthalmic lens comprising an UV-absorber and an anti-yellowing additive ESSILOR INTERNATIONAL (FR) 2019-08-06 US disclosed
US-20170121498-A1 Composition for the Manufacture of an Ophthalmic Lens Comprising an UV-Absorber and an Anti-Yellowing Additive ESSILOR INTERNATIONAL (FR) 2017-05-04 US disclosed
EP-3161528-A1 COMPOSITION FOR THE MANUFACTURE OF AN OPHTALMIC LENS COMPRISING AN UV-ABSORBER AND AN ANTI-YELLOWING ADDITIVE Essilor International (Compagnie Générale D'Optique) (FR) 2017-05-03 EP disclosed
EP-2960687-B1 COMPOSITION FOR THE MANUFACTURE OF AN OPHTALMIC LENS COMPRISING AN UV-ABSORBER AND AN ANTI-YELLOWING ADDITIVE ESSILOR INT (FR) 2016-09-21 EP disclosed
EP-2960687-A1 Composition for the manufacture of an ophtalmic lens comprising an uv-absorber and an anti-yellowing additive ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE) (FR) 2015-12-30 EP disclosed
US-20100201939-A1 PLASTIC LENS AND METHOD OF MANUFACTURING THE SAME HOYA CORPORATION (JP) 2010-08-12 US disclosed
EP-2172792-A1 PLASTIC LENS AND METHOD OF MANUFACTURING THE SAME Hoya Corporation (JP) 2010-04-07 EP disclosed
EP-1085349-B1 Plastic lenses having good ultraviolet absorbability, and method for the production thereof HOYA CORP (JP) 2006-06-28 EP disclosed
US-6448304-B1 POLYURETHANE, POLYTHIOURETHANE OR DIETHYLENE GLYCOL BISALLYLCARBONATE POLYMER; DIPPING IN SOLUTION CONTAINING A DIBENZOYLMETHANE OR A BENZOTRIZOLE COMPOUND; PLASTIC LENS FOR SPECTACLES WHICH ABSORBS ULTRAVIOLET RAYS; LOW YELLOWNESS HOYA CORPORATION (JP) 2002-09-10 US disclosed
EP-1144391-A1 ONE-POT PROCESS FOR THE PREPARATION OF 5-SULFONYL-SUBSTITUTED BENZOTRIAZOLES Ciba SC Holding AG (CH) 2001-10-17 EP disclosed
EP-1085349-A2 Plastic lenses having good ultraviolet absorbability, and method for the production thereof HOYA CORPORATION (JP) 2001-03-21 EP disclosed
WO-2000043376-A1 ONE-POT PROCESS FOR THE PREPARATION OF 5-SULFONYL-SUBSTITUTED BENZOTRIAZOLES CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-07-27 WO disclosed
US-6040455-A REACTING A HALOBENZOTRIAZOLE COMPOUND WITH ALIPHATIC, PHENYLALKYL OR ARYL MERCAPTAN COMPOUND TO FORM 5-THIO SUBSTITUTED BENZOTRIAZOLE, OXIDIZING WITH HYDROGEN PEROXIDE TO FOR 5-SULFONE SUBSTITUED BENZOTRIAZOLE COMPOUND CIBA SPECIALTY CHEMICALS CORPORATION (US) 2000-03-21 US disclosed