SCHEMBL2949019

SCHEMBL2949019

CCc1ccc(C(=CC=C(c2ccccc2)c2ccccc2)c2ccc(CC)c(CC)c2N)c(N)c1CC

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS2 P35354 5/20 0.38
PTGS1 P23219 4/20 0.38
MTNR1A P48039 1/20 0.33
MTNR1B P49286 1/20 0.33
ALDH1A1 P00352 2/20 0.32
RAB9A P51151 2/20 0.32
SMN1; SMN2 Q16637 2/20 0.32
NPC1 O15118 1/20 0.32
PKM P14618 1/20 0.32
CES2 O00748 1/20 0.31
CES1 P23141 1/20 0.31
NPSR1 Q6W5P4 3/20 0.30
MAPT P10636 4/20 0.30
GAA P10253 2/20 0.30
LMNA P02545 2/20 0.30
HTT P42858 2/20 0.30
L3MBTL1 Q9Y468 1/20 0.30
CYP3A4 P08684 1/20 0.30
CYP2D6 P10635 1/20 0.30
CYP2C9 P11712 1/20 0.30

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
SCHEMBL743150 0.80 MAPT (0.47) PTGS2PTGS1ALDH1A1MAPTGAA
SCHEMBL9152453 0.79 MAPT (0.32) MTNR1AMTNR1BALDH1A1RAB9ASMN1; SMN2
SCHEMBL5169474 0.74 GABRP (0.47) ALDH1A1RAB9ASMN1; SMN2MAPTGAA
SCHEMBL4091414 0.71 PTGS1 (0.49) PTGS2PTGS1ALDH1A1MAPTGAA
SCHEMBL10751483 0.71 HSD17B1 (0.42) ALDH1A1CYP3A4
SCHEMBL6607453 0.71 GABRP (0.36) ALDH1A1SMN1; SMN2MAPTLMNACYP3A4
SCHEMBL22423598 0.69 MTNR1A (0.39) MTNR1AMTNR1BCES2CES1NPSR1
Hydrochloric Acid SCHEMBL6639008 0.69 GABRP (0.35) ALDH1A1SMN1; SMN2MAPTLMNACYP3A4
SCHEMBL28262959 0.69 HSP90AB1 (0.42) ALDH1A1SMN1; SMN2MAPTL3MBTL1
SCHEMBL2692610 0.69 GABRP (0.32)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7754403-B2 asymmetric bishydroxy compound having an excellent charge transporting performance as well as excellent solubility in the solvent and compatibility with the resin where no partial crystals are created at the time of film formation, and electrical properties and durability are both excellent SHARP KABUSHIKI KAISHA (JP) 2010-07-13 US disclosed
US-20070207395-A1 Electrophotoconductor and image forming apparatus SHARP KABUSHIKI KAISHA (JP) 2007-09-06 US disclosed