SCHEMBL5317124

SCHEMBL5317124

COc1ccc([C@H](C#N)O[Si](C)(C)C)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 12/20 0.47
GAA P10253 4/20 0.47
LMNA P02545 2/20 0.44
HTT P42858 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.41
PBRM1 Q86U86 1/20 0.41
CA1 P00915 2/20 0.39
CA2 P00918 2/20 0.39
CA12 O43570 1/20 0.39
CA7 P43166 1/20 0.39
CA9 Q16790 1/20 0.39
CA14 Q9ULX7 1/20 0.39
NPC1 O15118 2/20 0.39
RAB9A P51151 2/20 0.39
PKM P14618 1/20 0.39
TSHR P16473 2/20 0.39
MAPK1 P28482 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
KDM4E B2RXH2 2/20 0.38

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
SCHEMBL1789913 1.00 ALDH1A1 (0.47) ALDH1A1GAALMNAHTTSMN1; SMN2
SCHEMBL7932437 0.86 ALDH1A1 (0.33) ALDH1A1GAALMNAHTT
SCHEMBL9297323 0.83 ALDH1A1 (0.43) ALDH1A1GAALMNAHTTSMN1; SMN2
SCHEMBL5525306 0.83 ALDH1A3 (0.37) ALDH1A1SMN1; SMN2MAPTKMT2A
SCHEMBL12412508 0.82 ALDH1A1 (0.39) ALDH1A1GAALMNAHTTNPC1
SCHEMBL6613625 0.82 CA1 (0.40) ALDH1A1GAAHTTCA1CA2
SCHEMBL7089384 0.81 ALDH1A1 (0.39) ALDH1A1GAALMNAHTTSMN1; SMN2
SCHEMBL7452976 0.81 LTA4H (0.40) ALDH1A1GAASMN1; SMN2TSHRTDP1
SCHEMBL14763050 0.80 PDE2A (0.41) ALDH1A1GAASMN1; SMN2NPC1RAB9A
SCHEMBL2610137 0.80 L3MBTL1 (0.42) ALDH1A1HTTCA1CA2CA7

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
WO-2007077141-A1 METHOD FOR PRODUCING SUBSTITUTED PHENYLACETYL CARBINOLS BASF AKTIENGESELLSCHAFT (DE) 2007-07-12 WO disclosed
US-5329023-A Method of preparing optically active alcohols which consist substantially or entirely of one enantiomer DUPHAR INTERNATIONAL RESEARCH B.V. (NL) 1994-07-12 US disclosed