SCHEMBL6151225

SCHEMBL6151225

C=CC(=O)OCCCCC[SiH](OC)OC

nearest known ligand 0.66

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
TSHR P16473 9/20 0.66
ALDH1A1 P00352 4/20 0.66
CYP3A4 P08684 2/20 0.66
HPGD P15428 1/20 0.55
TP53 P04637 3/20 0.46
HIF1A Q16665 3/20 0.46
HSD17B10 Q99714 1/20 0.46
THRB P10828 2/20 0.39
HCAR2 Q8TDS4 3/20 0.38
ATM Q13315 1/20 0.36
MAPK1 P28482 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
NAAA Q02083 1/20 0.32
HTT P42858 1/20 0.31
EPHX1 P07099 1/20 0.30

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
SCHEMBL23174784 1.00 TSHR (0.66) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL16286524 1.00 TSHR (0.66) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL80819 0.98 TSHR (0.62) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL139742 0.93 TSHR (0.59) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL28074744 0.91 TSHR (0.57) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL6440674 0.88 TSHR (0.50) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL108693 0.85 TSHR (0.52) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL8639379 0.84 TSHR (0.46) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL27152282 0.84 TSHR (0.45) TSHRALDH1A1CYP3A4HPGDTP53
SCHEMBL16286758 0.83 TSHR (0.61) 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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3310792-B1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW SILICONES CORP (US) 2021-07-21 EP claimed
EP-3310792-B1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW SILICONES CORP (US) 2021-07-21 EP disclosed
EP-3310793-B1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW SILICONES CORP (US) 2021-06-09 EP disclosed
US-10273254-B2 Process for preparing an acryloyloxysilane DOW CORNING CORPORATION (US) 2019-04-30 US disclosed
US-10246473-B2 Process for preparing an acryloyloxysilane DOW CORNING CORPORATION (US) 2019-04-02 US disclosed
EP-2785726-B1 ESTER-FUNCTIONAL SILANES AND THE PREPARATION AND USE THEREOF; AND USE OF IMINIUM COMPOUNDS AS PHASE TRANSFER CATALYSTS DOW SILICONES CORP (US) 2018-08-01 EP disclosed
US-20180155371-A1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW SILICONES CORPORATION 2018-06-07 US disclosed
US-20180134734-A1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW SILICONES CORPORATION 2018-05-17 US disclosed
US-9518072-B2 Ester-functional silanes and the preparation and use thereof; and use of iminium compounds as phase transfer catalysts DOW CORNING CORPORATION (US) 2016-12-13 US disclosed
EP-2762482-B1 PROCESS FOR PURIFYING AN ACRYLOYLOXYSILANE DOW CORNING (US) 2016-10-26 EP disclosed
US-9249164-B2 Process for preparing an acryloyloxysilane DOW SILICONES CORPORATION 2016-02-02 US disclosed
US-20150126676-A1 Ester-Functional Silanes And The Preparation And Use Thereof; And Use Of Iminium Compounds As Phase Transfer Catalysts DOW SILICONES CORPORATION 2015-05-07 US disclosed
EP-2621936-B1 PROCESS FOR PREPARING AN ACRYLOYLOXYSILANE DOW CORNING (US) 2014-10-22 EP disclosed
US-20130184482-A1 Process For Preparing An Acryloyloxysilane DOW CORNING CORPORATION (US) 2013-07-18 US disclosed
EP-1234830-B1 Method of preparing an organosilicon compound containing a methacryloxy functional group DOW CORNING TORAY SILICONE (JP) 2005-01-19 EP disclosed
US-6448427-B1 REACTING AN ALKALI-METAL SALT OF (METH)ACRYLIC ACID WITH A HALOGEN SUBSTITUTED ORGANOSILICON COMPOUND IN THE PRESENCE OF A TERTIARY AMINE DIAZABICYCLO DERIVATIVE DOW CORNING TORAY SILICONE CO., LTD. (JP) 2002-09-10 US disclosed
EP-1234830-A2 Method of preparing an organosilicon compound containing a methacryloxy functional group Dow Corning Toray Silicone Co., Ltd. (JP) 2002-08-28 EP disclosed
US-20020115878-A1 METHOD OF PREPARING AN ORGANOSILICON COMPOUND CONTAINING A METHACRYLOXY FUNCTIONAL GROUP DOW TORAY CO., LTD. (JP) 2002-08-22 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20150126676-A1 Ester-Functional Silanes And The Preparation And Use Thereof; And Use Of Iminium Compounds As Phase Transfer Catalysts ICMT, INTS9, HDHD5 TSHR 4158/4885ALDH1A1 2430/4885CYP3A4 195/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.