SCHEMBL7933562

SCHEMBL7933562

CC(O)Oc1ccc2c(=O)cc(-c3ccccc3)oc2c1

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP3A4 P08684 4/20 0.81
▸ SMN1; SMN2 Q16637 4/20 0.81
▸ TP53 P04637 4/20 0.81
▸ MAPT P10636 3/20 0.81
▸ MEN1 O00255 2/20 0.81
▸ KMT2A Q03164 2/20 0.81
▸ LMNA P02545 1/20 0.81
▸ CYP19A1 P11511 4/20 0.69
▸ TNKS O95271 2/20 0.69
▸ KDM4E B2RXH2 4/20 0.61
▸ MAOB P27338 3/20 0.60
▸ ABCB1 P08183 3/20 0.60
▸ CA12 O43570 2/20 0.60
▸ CA1 P00915 2/20 0.60
▸ CA2 P00918 2/20 0.60
▸ CYP1B1 Q16678 2/20 0.60
▸ CA9 Q16790 2/20 0.60
▸ AKR1B10 O60218 1/20 0.60
▸ CYP1A2 P05177 1/20 0.60
▸ CALM1 P0DP23 1/20 0.60

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
SCHEMBL27618931 0.89 SMN1; SMN2 (0.76) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL27493025 0.89 SMN1; SMN2 (1.00) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL30540840 0.89 SMN1; SMN2 (1.00) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL31499219 0.85 CYP3A4 (0.77) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL4160583 0.84 TNKS (0.64) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL4172232 0.83 MAPT (0.74) CYP3A4SMN1; SMN2TP53MAPTMEN1
7-Methoxyflavone SCHEMBL1373009 0.82 TNKS (1.00) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL4166841 0.82 MEN1 (0.55) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL28639665 0.80 MAPT (0.82) CYP3A4SMN1; SMN2TP53MAPTMEN1
SCHEMBL27609731 0.80 ABCB1 (0.69) CYP3A4SMN1; SMN2TP53MAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6245922-B1 PREPARED BY REACTING AN ELECTROPHILIC 2-ALKENYL AZALACTONE WITH A NUCLEOPHILIC AROMATIC KETONE; CAN BE COPOLYMERIZED WITH ACRYLIC MONOMERS AND PHOTOACTIVATED BY ACTINIC RADIATION TO CROSSLINK THE POLYMERS 3M INNOVATIVE PROPERTIES COMPANY 2001-06-12 — — US disclosed
EP-0837844-B1 ACRYLAMIDE DERIVATIVES AS CHROMOPHORIC PHOTOCROSSLINKING COMPOUND MINNESOTA MINING & MFG (US) 2000-04-05 — — EP disclosed
EP-0837844-A1 ACRYLAMIDE DERIVATIVES AS CHROMOPHORIC PHOTOCROSSLINKING COMPOUND MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-04-29 — — EP disclosed
WO-1997005101-A1 ACRYLAMIDE DERIVATIVES AS CHROMOPHORIC PHOTOCROSSLINKING COMPOUND MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-02-13 — — WO disclosed
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