SCHEMBL2491513

SCHEMBL2491513

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

nearest known ligand 0.37

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.37
THRB P10828 1/20 0.32
ALDH1A1 P00352 1/20 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
SCHEMBL3278987 0.87 TSHR (0.39) TSHRTHRBALDH1A1
SCHEMBL5308928 0.83 TSHR (0.35) TSHRTHRBALDH1A1
SCHEMBL29076717 0.83 TSHR (0.36) TSHRTHRBALDH1A1
SCHEMBL1014718 0.80 ALDH1A1 (0.40) TSHRTHRBALDH1A1
SCHEMBL9860071 0.78 TSHR (0.36) TSHRTHRBALDH1A1
Hydrogen Sulfide SCHEMBL21253275 0.78 ALDH1A1 (0.39) TSHRTHRBALDH1A1
SCHEMBL2496761 0.77 TSHR (0.37) TSHR
Hydrogen Sulfide SCHEMBL23421906 0.77 THRB (0.37) TSHRTHRBALDH1A1
SCHEMBL29022836 0.77 TSHR (0.39) TSHRTHRBALDH1A1
SCHEMBL8462711 0.77 TSHR (0.35) TSHRTHRBALDH1A1

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