SCHEMBL14401526

SCHEMBL14401526

C=CC(/C=C/c1cc(OC)c(OC)c(OC)c1)=C\C=N\CCSSCC[n+]1ccc(/C=C/c2cc(OC)c(OC)c(OC)c2)cc1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PSMB11 A5LHX3 1/20 0.40
▸ PSMA7 O14818 1/20 0.40
▸ PSMB1 P20618 1/20 0.40
▸ PSMA1 P25786 1/20 0.40
▸ PSMA2 P25787 1/20 0.40
▸ PSMA3 P25788 1/20 0.40
▸ PSMA4 P25789 1/20 0.40
▸ PSMB8 P28062 1/20 0.40
▸ PSMB9 P28065 1/20 0.40
▸ PSMA5 P28066 1/20 0.40
▸ PSMB4 P28070 1/20 0.40
▸ PSMB6 P28072 1/20 0.40
▸ PSMB5 P28074 1/20 0.40
▸ PSMB10 P40306 1/20 0.40
▸ PSMB3 P49720 1/20 0.40
▸ PSMB2 P49721 1/20 0.40
▸ PSMA6 P60900 1/20 0.40
▸ PSMA8 Q8TAA3 1/20 0.40
▸ PSMB7 Q99436 1/20 0.40
▸ BACE1 P56817 1/20 0.39

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
SCHEMBL14401515 0.84 CYP1A1 (0.42) BACE1CYP1A1CYP1A2CYP1B1KDM4E
SCHEMBL14401518 0.84 CYP1A1 (0.40) BACE1CYP1A1CYP1A2CYP1B1KDM4E
SCHEMBL13694972 0.83 APP (0.47) HTTKDM4EALDH1A1HPGD
SCHEMBL19649207 0.82 BACE1 (0.43) BACE1CYP1A1CYP1A2CYP1B1NQO2
SCHEMBL16070280 0.81 APP (0.32) —
SCHEMBL12451468 0.81 KDM4A (0.43) CYP1A2GAAHTTALDH1A1
SCHEMBL16104210 0.80 PSMB11 (0.40) PSMB11PSMA7PSMB1PSMA1PSMA2
SCHEMBL14401403 0.79 TUBB1 (0.57) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL18559995 0.78 BACE1 (0.40) BACE1CYP19A1
SCHEMBL21005628 0.78 — —

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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