SCHEMBL13891773

SCHEMBL13891773

C=CC(=O)Cc1ccc(-c2ccc(N(c3ccccc3)c3cccc(C)c3)cc2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 4/20 0.41
HTT P42858 2/20 0.41
NPC1 O15118 2/20 0.41
ALDH1A1 P00352 2/20 0.41
JAK2 O60674 1/20 0.41
PAX8 Q06710 1/20 0.41
LTB4R2 Q9NPC1 1/20 0.40
HSD17B1 P14061 1/20 0.40
HSD17B2 P37059 1/20 0.40
NR1H4 Q96RI1 1/20 0.39
KMT2A Q03164 5/20 0.39
MEN1 O00255 4/20 0.39
ABCC4 O15439 1/20 0.38
LMNA P02545 1/20 0.38
GAA P10253 1/20 0.38
TSHR P16473 1/20 0.38
PTGS1 P23219 1/20 0.38
CNR2 P34972 1/20 0.36
HPGD P15428 1/20 0.36
ALOX15 P16050 1/20 0.36

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
SCHEMBL13891756 0.97 HSD17B1 (0.41) RAB9AHTTNPC1ALDH1A1JAK2
Acrylic Acid SCHEMBL2282119 0.86 HSD17B1 (0.46) RAB9AHTTNPC1ALDH1A1JAK2
SCHEMBL12571982 0.85 LMNA (0.38) HTTALDH1A1LTB4R2ABCC4LMNA
SCHEMBL14410123 0.84 ALDH1A1 (0.42) HTTALDH1A1KMT2AMEN1ABCC4
SCHEMBL20733435 0.84 ALDH1A1 (0.42) HTTALDH1A1KMT2AMEN1ABCC4
SCHEMBL13891757 0.83 RAB9A (0.41) RAB9AHTTNPC1ALDH1A1JAK2
SCHEMBL12751304 0.80 CRHBP (0.40) ALDH1A1KMT2ATSHRGLA
SCHEMBL12934616 0.80 BCL2 (0.42) HSD17B1HSD17B2KMT2AMEN1FFAR1
SCHEMBL22148976 0.80 LTB4R2 (0.39) RAB9AHTTNPC1ALDH1A1JAK2
SCHEMBL9915683 0.79 THRB (0.42) RAB9AHTTNPC1ALDH1A1JAK2

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