SCHEMBL2496766

SCHEMBL2496766

C=CC(=O)OCCC[SiH2]OC(C(C)C)C(C)C

nearest known ligand 0.52

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
TSHR P16473 7/20 0.52
ALDH1A1 P00352 4/20 0.52
CYP3A4 P08684 2/20 0.52
HPGD P15428 1/20 0.51
TP53 P04637 3/20 0.43
HIF1A Q16665 3/20 0.43
HSD17B10 Q99714 1/20 0.43
THRB P10828 2/20 0.37
ATM Q13315 1/20 0.34
MAPK1 P28482 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
HCAR2 Q8TDS4 2/20 0.31

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
SCHEMBL1014595 0.89 TSHR (0.53) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL229761 0.84 TSHR (0.53) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL27541005 0.83 TSHR (0.47) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL7879592 0.83 TSHR (0.54) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL1803889 0.82 TSHR (0.53) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL7511201 0.81 TSHR (0.52) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL393550 0.80 TSHR (0.47) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL20555649 0.80 TSHR (0.51) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL336349 0.80 TSHR (0.59) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL7880363 0.79 TSHR (0.54) TSHRALDH1A1CYP3A4HPGDTP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7279527-B2 Method of converting anionic living end to protected free radical living end and applications thereof BRIDGESTONE CORPORATION (JP) 2007-10-09 US claimed
US-20060241265-A1 Method of converting anionic living end to protected free radical living end and applications thereof BRIDGESTONE CORPORATION (JP) 2006-10-26 US claimed
US-6376615-B1 USING FREE RADICALS CENTRO DE INVESTIGACION EN QUIMICA APLICADA (MX) 2002-04-23 US claimed
US-8030410-B2 Reacting anionic living end polymer that is end capped with steric hindering carbonyl-containing compound to produce polymer with homolytically cleaveable group; engineering plastics BRIDGESTONE CORPORATION (JP) 2011-10-04 US disclosed
US-7737218-B2 Method for generating free radical capable polymers using tin or silicon halide compounds BRIDGESTONE CORPORATION (JP) 2010-06-15 US disclosed
US-7560509-B2 Method of directing grafting by controlling the location of high vinyl segments in a polymer BRIDGESTONE CORPORATION (JP) 2009-07-14 US disclosed
US-20080161495-A1 Method for Generating Free Radical Capable Polymers Using Tin or Silicon Halide Compounds BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-20080161484-A1 Method of Directing Grafting by Controlling the Location of High Vinyl Segments in a Polymer BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-20080161501-A1 Method for generating free radical capable polymers using carbonyl-containing compounds BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-7279527-B2 Method of converting anionic living end to protected free radical living end and applications thereof BRIDGESTONE CORPORATION (JP) 2007-10-09 US disclosed
US-20060241265-A1 Method of converting anionic living end to protected free radical living end and applications thereof BRIDGESTONE CORPORATION (JP) 2006-10-26 US disclosed
US-6376615-B1 USING FREE RADICALS CENTRO DE INVESTIGACION EN QUIMICA APLICADA (MX) 2002-04-23 US disclosed