SCHEMBL5199356

SCHEMBL5199356

CCNCCC[SiH](OC)OC

nearest known ligand 0.48

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 2/20 0.48
MEN1 O00255 1/20 0.48
GLA P06280 1/20 0.48
KMT2A Q03164 1/20 0.48
TSHR P16473 2/20 0.46
CYP1A2 P05177 1/20 0.46
KDM1A O60341 5/20 0.39
SAT1 P21673 3/20 0.37
TP53 P04637 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
Ammonia Solution, Strong SCHEMBL28256574 0.98 CYP2C19 (0.46) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL550550 0.93 CYP2C19 (0.50) CYP2C19MEN1GLAKMT2ATSHR
Ammonia Solution, Strong SCHEMBL10482132 0.91 CYP2C19 (0.48) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL15360653 0.91 CYP2C19 (0.48) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL16100183 0.87 CYP2C19 (0.35) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL16782934 0.85 CYP2C19 (0.39) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL23252205 0.84 TSHR (0.40) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL15360341 0.84 TSHR (0.46) CYP2C19MEN1GLAKMT2ATSHR
Diethylamine SCHEMBL28656264 0.81 TSHR (0.40) CYP2C19MEN1GLAKMT2ATSHR
SCHEMBL15004595 0.80 TSHR (0.54) CYP2C19TSHRCYP1A2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119630725-A Method for producing storage-stable activators for glass and ceramic substrates SIKA技术股份公司 2025-03-14 CN disclosed
CN-118632907-A Method for producing storage-stable aqueous primers for glass and ceramic substrates SIKA技术股份公司 2024-09-10 CN disclosed
US-20240059088-A1 SILICA ENCAPSULATED PIGMENTS FOR NANO-METALLOGRAPHY ECKART GMBH (DE) 2024-02-22 US disclosed
EP-4274741-A1 SILICA ENCAPSULATED PIGMENTS FOR NANO-METALLOGRAPHY ECKART GmbH (DE) 2023-11-15 EP disclosed
WO-2022148658-A1 SILICA ENCAPSULATED PIGMENTS FOR NANO-METALLOGRAPHY ECKART GMBH (DE) 2022-07-14 WO disclosed
EP-3253829-B1 METHOD OF FORMING A PASSIVATED PIGMENT SLURRY FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF COATINGS GMBH (DE) 2020-09-16 EP disclosed
EP-3487941-B1 METHOD OF FORMING A SLURRY OF ENCAPSULATED PIGMENT FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF COATINGS GMBH (DE) 2020-09-09 EP disclosed
EP-3487941-A1 METHOD OF FORMING A SLURRY OF ENCAPSULATED PIGMENT FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF Coatings GmbH (DE) 2019-05-29 EP disclosed
US-10273371-B2 Method of forming a slurry of encapsulated pigment for an aqueous topcoat coating composition BASF COATINGS GMBH (DE) 2019-04-30 US disclosed
WO-2018019628-A1 METHOD OF FORMING A SLURRY OF ENCAPSULATED PIGMENT FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF COATINGS GMBH (DE) 2018-02-01 WO disclosed
US-9777180-B2 Method of forming a passivated pigment slurry for an aqueous topcoat coating composition BASF COATINGS GMBH (DE) 2017-10-03 US disclosed
WO-2016126677-A1 METHOD OF FORMING A PASSIVATED PIGMENT SLURRY FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF COATINGS GMBH (DE) 2016-08-11 WO disclosed
US-20160222241-A1 METHOD OF FORMING A PASSIVATED PIGMENT SLURRY FOR AN AQUEOUS TOPCOAT COATING COMPOSITION BASF COATINGS GMBH (DE) 2016-08-04 US disclosed
EP-2660244-B1 Organoxysilane compounds having silyl-protected secondary amino group and making method SHINETSU CHEMICAL CO (JP) 2016-02-10 EP disclosed
US-9024051-B2 Organoxysilane compounds having silyl-protected secondary amino group and making method SHIN-ETSU CHEMICAL CO., LTD. (JP) 2015-05-05 US disclosed
US-20130296593-A1 ORGANOXYSILANE COMPOUNDS HAVING SILYL-PROTECTED SECONDARY AMINO GROUP AND MAKING METHOD SHIN-ETSU CHEMICAL CO., LTD. (JP) 2013-11-07 US disclosed
EP-2660244-A1 Organoxysilane compounds having silyl-protected secondary amino group and making method Shin-Etsu Chemical Co., Ltd. (JP) 2013-11-06 EP disclosed
US-7172812-B2 surface treatment of flake metal pigment Eckart-Werke Standard Bronzepūlver-Werke Carl-Eckart GmbH & Co. (DE) 2007-02-06 US disclosed
US-20040226480-A1 surface treatment of flake metal pigment ECKART-WERKE STANDARD BRONZEPULVER-WERKE CARL-ECKART GMBH & CO. 2004-11-18 US disclosed
US-6761762-B1 AGITATING AND HEATING INITIAL PIGMENT IN ORGANIC SOLVENT, MIXING PIGMENT WITH SOLUTION OF BASE IN WATER OR ANOTHER SOLVENT, ADDING ORGANIC SOLVENT BASED SURFACE-MODIFYING AGENT TO MIXTURE, COOLING, REMOVING LIQUID TO FORM FILTER CAKE ECKART-WERKE STANDARD BRONZEPULVER-WERKER CARL-ECKART GMBH & CO. (DE) 2004-07-13 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-20130296593-A1 ORGANOXYSILANE COMPOUNDS HAVING SILYL-PROTECTED SECONDARY AMINO GROUP AND MAKING METHOD AS3MT, SUGT1, PNMT CYP2C19 4290/4885MEN1 3135/4885GLA 3681/4885

“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.