SCHEMBL3335756

SCHEMBL3335756

CO[Si](C)(C)CCOC(C)=O

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.43
CHRM5 P08912 2/20 0.41
CHRM1 P11229 2/20 0.41
CHRM3 P20309 2/20 0.41
PGR P06401 1/20 0.41
CHRM2 P08172 1/20 0.41
CHRM4 P08173 1/20 0.41
HTR1A P08908 1/20 0.41
CHRNB2 P17787 1/20 0.41
TBXA2R P21731 1/20 0.41
CHRNB4 P30926 1/20 0.41
CHRNA3 P32297 1/20 0.41
CHRNA7 P36544 1/20 0.41
CHRNA4 P43681 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
CHRNA10 Q9GZZ6 1/20 0.41
CHRNA9 Q9UGM1 1/20 0.41
TSHR P16473 1/20 0.41
GALR3 O60755 2/20 0.40
GAA P10253 1/20 0.40

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
SCHEMBL3341112 0.87 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL1473802 0.82 ALDH1A1 (0.43) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL13151001 0.82 ALDH1A1 (0.43) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL13551155 0.80 ALDH1A1 (0.41) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL675935 0.79 THRB (0.48) ALDH1A1TSHRHTT
SCHEMBL141448 0.79 ALDH1A1 (0.44) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL13151033 0.78 NAAA (0.45) ALDH1A1TSHRGAAHTTCYP1A2
SCHEMBL3338087 0.78 ALDH1A1 (0.48) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL826515 0.78 ALDH1A1 (0.48) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL333436 0.77

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170373347-A1 POLYMER ELECTROLYTE, METHOD OF PREPARING THE POLYMER ELECTROLYTE, AND LITHIUM METAL BATTERY INCLUDING THE SAME SAMSUNG ELECTRONICS CO., LTD. (KR) 2017-12-28 US disclosed
US-8968458-B2 Composition for resist underlayer film and process for producing same JSR CORPORATION (JP) 2015-03-03 US disclosed
US-8808446-B2 Composition for resist underlayer film and process for producing same JSR CORPORATION (JP) 2014-08-19 US disclosed
US-7799469-B2 electrolytic salt e.g. LiPF6 is dissolved in an organic solvent ( ethylene carbonate, vinyline carbonate, diethyl carbonate) and a silicon compound additive; increase of internal resistance in storage at high temperature; stable power souce for hybrid or battery cars using electrical power; green energy DENSO CORPORATION (JP) 2010-09-21 US disclosed
US-20100151384-A1 COMPOSITION FOR RESIST UNDERLAYER FILM AND PROCESS FOR PRODUCING SAME JSR CORPORATION (JP) 2010-06-17 US disclosed
US-20090050020-A1 COMPOSITION FOR RESIST UNDERLAYER FILM AND PROCESS FOR PRODUCING SAME JSR CORPORATION (JP) 2009-02-26 US disclosed
EP-1855159-A1 COMPOSITION FOR UNDERLAYER FILM OF RESIST AND PROCESS FOR PRODUCING THE SAME JSR Corporation (JP) 2007-11-14 EP disclosed
US-20070243470-A1 electrolytic salt e.g. LiPF6 is dissolved in an organic solvent ( ethylene carbonate, vinyline carbonate, diethyl carbonate) and a silicon compound additive; increase of internal resistance in storage at high temperature; stable power souce for hybrid or battery cars using electrical power; green energy DENSO CORPORATION (JP) 2007-10-18 US disclosed
EP-0073027-B1 MASTERBATCH COMPOSITION COMPRISING A MATRIX HAVING A POLYSILOXANE DISPERSED THEREIN AND A METHOD FOR THE PREPARATION THEREOF UNION CARBIDE CORPORATION (US) 1987-05-06 EP disclosed
EP-0073027-A2 Masterbatch composition comprising a matrix having a polysiloxane dispersed therein and a method for the preparation thereof UNION CARBIDE CORPORATION (US) 1983-03-02 EP disclosed