SCHEMBL7923749

SCHEMBL7923749

O=c1c2ccccc2sc2cccc(OCCO)c12

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.48
RAB9A P51151 3/20 0.48
MAPT P10636 2/20 0.48
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2C9 P11712 1/20 0.48
HPGD P15428 1/20 0.48
CYP2C19 P33261 1/20 0.48
MAOA P21397 10/20 0.48
MAOB P27338 10/20 0.48
TDP1 Q9NUW8 1/20 0.42
IDO1 P14902 1/20 0.42
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
ALDH1A1 P00352 1/20 0.42
POLB P06746 1/20 0.42
GAA P10253 1/20 0.42
MCL1 Q07820 2/20 0.41
BCL2 P10415 1/20 0.41
BCL2L1 Q07817 1/20 0.41

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
SCHEMBL30162125 0.92 NPC1 (0.44) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL30162240 0.92 NPC1 (0.44) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL31730228 0.86 NPC1 (0.48) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL7051376 0.86 NPC1 (0.51) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL1254776 0.86 NPC1 (0.48) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL15549093 0.85 LMNA (0.48) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL28004808 0.84 NPC1 (0.47) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL24948345 0.84 MAPT (0.44) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL11169380 0.84 MAPT (0.44) NPC1RAB9AMAPTCYP1A2CYP3A4
SCHEMBL3252488 0.82 MAPT (0.54) NPC1RAB9AMAPTCYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115279744-A Modified thioxanthone photoinitiators 林特弗德有限公司 2022-11-01 CN claimed
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