SCHEMBL598317

SCHEMBL598317

O=C(OC(c1cc2ccccc2c2ccccc12)c1cc2ccccc2c2ccccc12)[C@H](Cc1ccccc1)c1ccccc1

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CHRM1 P11229 6/20 0.45
EPHX1 P07099 1/20 0.44
BACE1 P56817 1/20 0.39
BACE2 Q9Y5Z0 1/20 0.39
ACP3 P15309 3/20 0.39
ESR1 P03372 1/20 0.38
ESR2 Q92731 1/20 0.38
UBE2N P61088 1/20 0.38
CYP1A2 P05177 1/20 0.36
CYP2D6 P10635 1/20 0.36
CYP2C19 P33261 1/20 0.36
PPARG P37231 1/20 0.36
PPARA Q07869 1/20 0.36
HCRTR2 O43614 1/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35

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
SCHEMBL598409 0.86 KDM4E (0.43) MEN1KMT2A
SCHEMBL598830 0.85 ACP3 (0.49) CHRM1EPHX1BACE1BACE2ACP3
SCHEMBL600006 0.79 TACR3 (0.43) CYP1A2CYP2D6CYP2C19MEN1KMT2A
SCHEMBL599493 0.71 AKR1B1 (0.39) KMT2A
SCHEMBL599640 0.70 KDM4E (0.45) MEN1KMT2A
SCHEMBL598171 0.70 UTS2R (0.38) ACP3MEN1KMT2A
SCHEMBL599408 0.69 TDP1 (0.49) CYP1A2PPARGMEN1KMT2A
SCHEMBL14691416 0.69 CHRM1 (0.63) CHRM1EPHX1ESR1ESR2UBE2N
SCHEMBL10691182 0.69 EPHX1 (0.61) CHRM1EPHX1ACP3ESR1ESR2
SCHEMBL14384902 0.69 EPHX1 (0.61) CHRM1EPHX1ACP3ESR1ESR2

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-8115008-B2 Method for producing optically active ester and method for producing optically active carboxylic acid TOKYO UNIVERSITY OF SCIENCE EDUCATION FOUNDATION ADMINISTRATIVE ORGANIZATION (JP) 2012-02-14 US disclosed