SCHEMBL14401506

SCHEMBL14401506

COc1cc(OC)c(OC)cc1/C=C/c1ccccn1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 4/20 0.61
▸ KDM4E B2RXH2 3/20 0.61
▸ NPC1 O15118 2/20 0.61
▸ RAB9A P51151 2/20 0.61
▸ GAA P10253 1/20 0.61
▸ MAPK1 P28482 1/20 0.61
▸ MEN1 O00255 2/20 0.53
▸ KMT2A Q03164 2/20 0.53
▸ ATM Q13315 1/20 0.53
▸ CYP1A1 P04798 4/20 0.51
▸ CYP1B1 Q16678 4/20 0.51
▸ CYP1A2 P05177 3/20 0.51
▸ ALDH1A1 P00352 2/20 0.51
▸ HMGCR P04035 1/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ NFE2L2 Q16236 3/20 0.49
▸ HTT P42858 1/20 0.44
▸ PTGS1 P23219 1/20 0.44
▸ PTGS2 P35354 1/20 0.44
▸ ABCG2 Q9UNQ0 1/20 0.44

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
SCHEMBL19076160 0.83 NPC1 (0.74) MAPTKDM4ENPC1RAB9AGAA
SCHEMBL8854378 0.79 CYP1A1 (0.65) MAPTNPC1RAB9AGAACYP1A1
SCHEMBL22010235 0.79 CYP1A1 (0.65) MAPTNPC1RAB9AGAACYP1A1
SCHEMBL9189623 0.75 TUBB4A (0.65) MAPTKDM4ENPC1RAB9AGAA
SCHEMBL21005800 0.75 TUBB4A (0.65) MAPTKDM4ENPC1RAB9AGAA
SCHEMBL9189630 0.75 TUBB4A (0.65) MAPTKDM4ENPC1RAB9AGAA
SCHEMBL10385902 0.74 PTGS1 (0.65) MAPTKDM4ENPC1RAB9AGAA
Bromide SCHEMBL28082033 0.74 TUBB4A (0.63) MAPTKDM4ENPC1RAB9AGAA
SCHEMBL29256842 0.74 NPC1 (0.48) MAPTKDM4ENPC1RAB9AGAA
Methyl Alcohol SCHEMBL28478479 0.73 NPC1 (0.89) MAPTKDM4ENPC1RAB9AGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2007110540-A2 DYEING COMPOSITION CONTAINING A THIOL/DISULPHIDE FLUORESCENT COLORANT COMPRISING AN ALKOXY/HYDROXY GROUPING, WITH AN INTERNAL CATIONIC CHARGE, AND METHOD FOR LIGHTENING KERATIN MATERIALS USING SAID COLORANT L'OREAL (FR) 2007-10-04 — — WO disclosed
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