SCHEMBL216241

SCHEMBL216241

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

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.57
L3MBTL1 Q9Y468 2/20 0.57
MAPK1 P28482 2/20 0.57
HTT P42858 1/20 0.57
SMN1; SMN2 Q16637 3/20 0.44
MAPT P10636 3/20 0.44
PKM P14618 1/20 0.44
CDK5 Q00535 1/20 0.44
CDK5R1 Q15078 1/20 0.44
NPC1 O15118 1/20 0.41
RAB9A P51151 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
HSD17B10 Q99714 1/20 0.41
POLB P06746 1/20 0.41
TDP1 Q9NUW8 2/20 0.41
HPGD P15428 1/20 0.41
PPARA Q07869 1/20 0.40
ALDH1A1 P00352 2/20 0.39
ATM Q13315 1/20 0.39

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
SCHEMBL211644 0.84 LMNA (0.53) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL2043093 0.81 LMNA (0.39) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL2048653 0.81 LMNA (0.39) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL212674 0.81 ALDH1A1 (0.41) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL2043092 0.81 LMNA (0.39) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL9900481 0.77 CES2 (0.48) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL9900480 0.77 CES2 (0.48) LMNAL3MBTL1MAPK1HTTSMN1; SMN2
SCHEMBL2050607 0.76 PPARA (0.44) LMNAL3MBTL1MAPK1HTTPPARA
SCHEMBL2050606 0.76 PPARA (0.44) LMNAL3MBTL1MAPK1HTTPPARA
SCHEMBL17257007 0.76 LMNA (0.51) LMNAL3MBTL1MAPK1HTTSMN1; SMN2

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