SCHEMBL13891765

SCHEMBL13891765

C=C(C)C(=O)Cc1ccc(C2(c3ccc(N(c4ccc(C)cc4)c4ccc(C)cc4)cc3)CCCCC2)cc1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADORA3 P0DMS8 1/20 0.37
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
ESR1 P03372 3/20 0.35
ESR2 Q92731 3/20 0.35
CNR2 P34972 4/20 0.34
CNR1 P21554 3/20 0.34
PPARA Q07869 1/20 0.34
HSD11B1 P28845 2/20 0.34
HSD11B2 P80365 2/20 0.34
MEN1 O00255 2/20 0.33
HTT P42858 2/20 0.33
KMT2A Q03164 2/20 0.33
CYP3A4 P08684 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
MAPT P10636 1/20 0.33
HTR1E P28566 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
S1PR3 Q99500 1/20 0.33

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
SCHEMBL13891747 0.97 ITGB1 (0.35) ADORA3NPC1RAB9AESR1ESR2
SCHEMBL13891774 0.83 ADORA3 (0.37) ADORA3NPC1RAB9AESR1ESR2
SCHEMBL2602480 0.81 CA1 (0.42) ADORA3ESR1ESR2CNR2CNR1
SCHEMBL9915790 0.81 L3MBTL1 (0.42) NPC1RAB9ACNR2CNR1KMT2A
SCHEMBL13891772 0.81 ADORA3 (0.35) ADORA3NPC1RAB9AESR1ESR2
SCHEMBL13765741 0.79 HSD11B1 (0.41) ADORA3ESR1ESR2HSD11B1HSD11B2
SCHEMBL5452904 0.79 ESR1 (0.48) ADORA3ESR1ESR2HSD11B1HSD11B2
SCHEMBL13879208 0.79 ESR1 (0.48) ADORA3ESR1ESR2HSD11B1HSD11B2
SCHEMBL21168792 0.79 ESR1 (0.48) ADORA3ESR1ESR2HSD11B1HSD11B2
SCHEMBL12306231 0.79 ESR1 (0.48) ADORA3ESR1ESR2HSD11B1HSD11B2

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-7517625-B2 Electrophotographic photoreceptor with improved durability and wear resistance; high quality latent images; crosslinked charge transport layer has a hardened monomer having three or more functional groups without charge transport structure and one with charge transport-containing (meth)acryloyloxy groups RICOH COMPANY, LTD. (JP) 2009-04-14 US disclosed