SCHEMBL133944

SCHEMBL133944

CC(=O)OCCC[Si](Cl)(Cl)Cl

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.54
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
Methyl Alcohol SCHEMBL28209288 0.98 ALDH1A1 (0.52) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL7908273 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL19770568 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL2531847 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL1806859 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL29403870 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL19770552 0.91 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL12218721 0.88 ALDH1A1 (0.50) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL523168 0.86 ALDH1A1 (0.46) ALDH1A1CHRM5CHRM1CHRM3PGR
SCHEMBL524942 0.84 ALDH1A1 (0.52) ALDH1A1CHRM5CHRM1CHRM3PGR

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 127 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108059639-B Industrial synthesis method of acetoxypropyl trimethoxy silane 荆州市江汉精细化工有限公司 2020-05-19 CN claimed
CN-108059639-A A kind of industrial preparative method of acetyloxypropyl trimethoxy silane 荆州市江汉精细化工有限公司 2018-05-22 CN claimed
EP-2580294-B1 PVDF COATING COMPOSITIONS SOLVAY SOLEXIS SPA (IT) 2015-02-25 EP claimed
EP-2580294-A1 PVDF COATING COMPOSITIONS Solvay Solexis S.p.A. (IT) 2013-04-17 EP claimed
US-20130090417-A1 PVDF coating compositions SOLVAY SPECIALTY POLYMERS ITALY S.P.A. (IT) 2013-04-11 US claimed
WO-2011157657-A1 PVDF COATING COMPOSITIONS SOLVAY SOLEXIS S.P.A. (IT) 2011-12-22 WO claimed
WO-2004072140-A2 CROSSLINKED POLYESTER COPOLYMERS DUAN JIWEN F (US) 2004-08-26 WO claimed
US-6706842-B1 Crosslinked polyester copolymers DUAN JIWEN F (US) 2004-03-16 US claimed
EP-3687652-B1 HIGH PURITY CHROMATOGRAPHIC MATERIALS COMPRISING AN IONIZABLE MODIFIER FOR RETENTION OF ACIDIC ANALYTES WATERS TECHNOLOGIES CORP (US) 2025-07-09 EP disclosed
US-20240116025-A1 HYBRID MATERIAL FOR CHROMATOGRAPHIC SEPARATIONS COMPRISING A SUPERFICIALLY POROUS CORE AND A SURROUNDING MATERIAL WATERS TECHNOLOGIES CORPORATION (US) 2024-04-11 US disclosed
US-20230294073-A1 SUPERFICIALLY POROUS MATERIALS COMPRISING A COATED CORE HAVING NARROW PARTICLE SIZE DISTRIBUTION; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS WATERS TECHNOLOGIES CORPORATION (US) 2023-09-21 US disclosed
US-20230256413-A1 HIGH PURITY CHROMATOGRAPHIC MATERIALS COMPRISING AN IONIZABLE MODIFIER FOR RETENTION OF ACIDIC ANALYTES WATERS TECHNOLOGIES CORPORATION (US) 2023-08-17 US disclosed
US-11642653-B2 Hybrid material for chromatographic separations comprising a superficially porous core and a surrounding material WATERS TECHNOLOGIES CORPORATION (US) 2023-05-09 US disclosed
EP-4129466-A1 HIGH PURITY CHROMATROGRAPHIC MATERIALS COMPRISING AN IONIZABLE MODIFIER Waters Technologies Corporation (US) 2023-02-08 EP disclosed
WO-2003068289-A1 POLYMER COATING FOR MEDICAL DEVICES CV THERAPEUTICS, INC. (US) 2003-08-21 WO disclosed
US-4927750-A SEPARATION AND PURIFICATION OF BIOLOGICAL CELLS USING A COLLOIDAL SILICA, ORGANOSILANE REAGENT Simpson, Jeanette (US) 1990-05-22 US disclosed
US-4925963-A Process for reduction of organosilicon halides ETHYL CORPORATION (US) 1990-05-15 US disclosed
US-4329483-A FROM A CHLOROSILANE AND ACYLOXY COMPOUND; BY-PRODUCT INHIBITION DOW CORNING CORPORATION (US) 1982-05-11 US disclosed
US-4028384-A HYDROSILYLATION WITH A HYDROGEN SILANE, PLATINUM COMPLEX CATALYST DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1977-06-07 US disclosed
US-3950364-A PROCESS FOR THE PREPARATION OF ORGANIC SILICON COMPOUNDS DYNAMIT NOBEL AKTIENGESELLSCHAFT (DT) 1976-04-13 US disclosed