SCHEMBL28849429

SCHEMBL28849429

Cc1cccc([C@@]2(O)CCCC[C@@H]2Cc2ccccn2)c1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 P23975 7/20 0.46
SLC6A4 P31645 7/20 0.46
OPRM1 P35372 6/20 0.46
OPRD1 P41143 3/20 0.46
OPRK1 P41145 3/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
SLC22A1 O15245 3/20 0.44
CHRM2 P08172 1/20 0.44
CHRM1 P11229 1/20 0.44
SLC6A9 P48067 1/20 0.38
MAPT P10636 1/20 0.37
CYP1A2 P05177 1/20 0.37
CYP3A4 P08684 1/20 0.37
CYP2C19 P33261 1/20 0.37
TRPA1 O75762 1/20 0.36
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36
HTR2C P28335 1/20 0.36
HDAC4 P56524 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
SCHEMBL29950582 1.00 SLC6A2 (0.46) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849430 0.87 MAPT (0.39) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849438 0.87 MAPT (0.42) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849449 0.86 SLC6A4 (0.44) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL29950460 0.86 SLC6A4 (0.44) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL29950355 0.86 SLC6A2 (0.44) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849414 0.86 SLC6A2 (0.44) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849424 0.86 SLC6A4 (0.63) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL29950442 0.86 SLC6A4 (0.63) SLC6A2SLC6A4OPRM1OPRD1OPRK1
SCHEMBL28849415 0.83 SLC6A4 (0.42) SLC6A2SLC6A4OPRM1OPRD1OPRK1

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
CN-115108875-A Nitrogen-containing heteroarene chiral cyclic alcohol constructed by visible light asymmetric catalysis, and preparation method and application thereof 河南师范大学 2022-09-27 CN disclosed