SCHEMBL14230581

SCHEMBL14230581

CC(O)c1ccc(/C=C/c2ccccc2)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AHR P35869 1/20 0.48
▸ RELA Q04206 1/20 0.47
▸ TRPA1 O75762 1/20 0.47
▸ NFE2L2 Q16236 1/20 0.46
▸ CYP19A1 P11511 1/20 0.46
▸ MAOA P21397 1/20 0.46
▸ MAOB P27338 1/20 0.46
▸ MAPK1 P28482 2/20 0.46
▸ KDM4E B2RXH2 1/20 0.46
▸ UGT2B7 P16662 1/20 0.45
▸ TTR P02766 1/20 0.44
▸ ALOX5 P09917 1/20 0.44
▸ PTGS1 P23219 1/20 0.44
▸ PTGS2 P35354 1/20 0.44
▸ EGFR P00533 1/20 0.44
▸ CHAT P28329 1/20 0.43
▸ NPC1 O15118 1/20 0.43
▸ MTOR P42345 1/20 0.43
▸ TDP1 Q9NUW8 1/20 0.43
▸ TP53 P04637 1/20 0.43

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
SCHEMBL6546345 0.82 KDM4E (0.59) AHRRELATRPA1NFE2L2CYP19A1
SCHEMBL16105804 0.82 KDM4E (0.59) AHRRELATRPA1NFE2L2CYP19A1
SCHEMBL1666981 0.82 MAOB (0.50) RELATRPA1NFE2L2CYP19A1MAOA
SCHEMBL16105702 0.82 KDM4E (0.59) AHRRELATRPA1NFE2L2CYP19A1
SCHEMBL13476336 0.78 KDM4E (0.41) MAPK1KDM4EUGT2B7PTGS1PTGS2
Phenyl Ethanol SCHEMBL14782914 0.78 ALDH1A1 (0.61) KDM4EUGT2B7PTGS2TDP1TP53
Phenyl Ethanol SCHEMBL2165 0.78 — —
Phenyl Ethanol SCHEMBL7144 0.78 — —
Phenyl Ethanol SCHEMBL32685157 0.78 — —
Phenyl Ethanol SCHEMBL2164 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
US-7365141-B2 Solvent resistance; luminescent film-forming solvent processible polymer which contains cross-linking so as to increase its molar mass and to resist solvent dissolution, the cross-linking being such that the polymer retains semiconductive and luminescent properties; capable of charge transport CAMBRIDGE DISPLAY TECHNOLOGY LTD. (GB) 2008-04-29 — — US disclosed
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