SCHEMBL214457

SCHEMBL214457

CC(=NO[Si](Cc1ccccc1)(Cc1ccccc1)Cc1ccccc1)c1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.53
L3MBTL1 Q9Y468 2/20 0.53
MAPK1 P28482 2/20 0.53
HTT P42858 1/20 0.53
HPGD P15428 1/20 0.46
G6PC1 P35575 1/20 0.45
SMN1; SMN2 Q16637 3/20 0.43
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
MAPT P10636 2/20 0.42
PKM P14618 1/20 0.42
CDK5 Q00535 1/20 0.42
CDK5R1 Q15078 1/20 0.42
CYP1A2 P05177 1/20 0.40
CYP2D6 P10635 1/20 0.40
HSD17B10 Q99714 1/20 0.40
TDP1 Q9NUW8 2/20 0.39
ALOX12 P18054 1/20 0.39
PPARA Q07869 2/20 0.38
ALDH1A1 P00352 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
SCHEMBL214062 0.84 NOS2 (0.40) LMNAL3MBTL1MAPK1HTTG6PC1
SCHEMBL213215 0.80 SMN1; SMN2 (0.56) LMNAL3MBTL1HTTSMN1; SMN2NPC1
SCHEMBL214914 0.79 NOS2 (0.37) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL214915 0.79 NOS2 (0.37) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL215602 0.79 CYP1A2 (0.49) LMNAL3MBTL1HTTHPGDSMN1; SMN2
SCHEMBL212055 0.77 NPC1 (0.41) SMN1; SMN2NPC1RAB9APKMCYP1A2
SCHEMBL2045431 0.77 ALDH1A1 (0.35) LMNAL3MBTL1MAPK1HTTHPGD
SCHEMBL2045429 0.77 ALDH1A1 (0.35) LMNAL3MBTL1MAPK1HTTHPGD
SCHEMBL215432 0.76 RBBP9 (0.59) L3MBTL1MAPTPKMCYP1A2CYP2D6
SCHEMBL216241 0.76 LMNA (0.57) LMNAL3MBTL1MAPK1HTTHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8088868-B2 oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis BRIDGESTONE CORPORATION (JP) 2012-01-03 US claimed
US-20080146745-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2008-06-19 US claimed
US-8088868-B2 oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis BRIDGESTONE CORPORATION (JP) 2012-01-03 US disclosed
US-20080146745-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2008-06-19 US disclosed