SCHEMBL3289166

SCHEMBL3289166

Cc1ccc([S+]([O-])c2ccccc2)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 3/20 0.48
ALOX12 P18054 2/20 0.48
LMNA P02545 2/20 0.48
TSHR P16473 1/20 0.48
HPGD P15428 3/20 0.41
TDP1 Q9NUW8 3/20 0.40
CES2 O00748 1/20 0.38
CES1 P23141 1/20 0.38
CA12 O43570 3/20 0.36
CA9 Q16790 3/20 0.36
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
HTT P42858 2/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
NPC1 O15118 2/20 0.34
RAB9A P51151 2/20 0.34
CYP2C19 P33261 2/20 0.34
POLB P06746 2/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34

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
SCHEMBL20198275 1.00 ACHE (0.48) ACHEALOX12LMNATSHRHPGD
SCHEMBL12283588 1.00 ACHE (0.48) ACHEALOX12LMNATSHRHPGD
SCHEMBL20198276 0.93 ACHE (0.42) ACHEALOX12LMNATSHRHPGD
SCHEMBL4401131 0.89 ACHE (0.50) ACHEALOX12LMNATSHRTDP1
SCHEMBL235851 0.89 ACHE (0.50) ACHEALOX12LMNATSHRTDP1
SCHEMBL12336893 0.87 TDP1 (0.35) ACHEALOX12LMNATSHRTDP1
(Phenylsulfinyl)Benzene SCHEMBL43199 0.84 TDP1 (0.37) ACHEALOX12LMNATSHRHPGD
SCHEMBL31010991 0.83 ACHE (0.39) ACHEALOX12LMNATSHRHPGD
SCHEMBL4401181 0.82 ACHE (0.42) ACHELMNAHPGDTDP1CA9
SCHEMBL3289160 0.82 ACHE (0.42) ACHELMNAHPGDTDP1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118580164-A Preparation method of sulfoxide derivative 华侨大学 2024-09-03 CN claimed
US-9469604-B2 Method of manufacturing sulfonium salt TOYO GOSEI CO., LTD. (JP) 2016-10-18 US claimed
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 US disclosed
CN-118580164-A Preparation method of sulfoxide derivative 华侨大学 2024-09-03 CN disclosed
EP-3681933-B1 POLYMER-METAL JUNCTION SOLVAY SPECIALTY POLYMERS USA (US) 2024-05-15 EP disclosed
EP-3896114-B1 POLYIMIDE RESIN AND METHOD OF PRODUCING THE SAME, PHOTOSENSITIVE RESIN COMPOSITION, PATTERNING METHOD AND METHOD OF FORMING CURED FILM, INTERLAYER INSULATING FILM, SURFACE PROTECTIVE FILM, AND ELECTRONIC COMPONENT SHINETSU CHEMICAL CO (JP) 2023-10-18 EP disclosed
US-11359120-B2 Polymer-metal junction SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2022-06-14 US disclosed
US-20220149436-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2022-05-12 US disclosed
US-11283107-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2022-03-22 US disclosed
US-20210122953-A1 POLYMER-METAL JUNCTION SOLVAY SPECIALITY POLYMERS USA, LLC 2021-04-29 US disclosed
EP-3681933-A1 POLYMER-METAL JUNCTION Solvay Specialty Polymers USA, LLC (US) 2020-07-22 EP disclosed
US-5446172-A Reacting diarylsulfoxide and aromatic substrate in the presence of phosphorus pentoxide and methanesulfonic acid to produce triarylsulfonium complex, metathesizing with alkali metal hexafluoro metal salt GENERAL ELECTRIC COMPANY (US) 1995-08-29 US disclosed
EP-0455083-B1 Method for making triarylsulfonium hexafluorometal or metalloid salts GEN ELECTRIC (US) 1995-03-01 EP disclosed
EP-0212375-B1 MODERATED REDUCTION REACTIONS FOR PRODUCING ARYLHYDROXYLAMINES MicroSi, Inc. (a Delaware corporation) (US) 1993-06-16 EP disclosed
EP-0455083-A1 Method for making triarylsulfonium hexafluorometal or metalloid salts GENERAL ELECTRIC COMPANY (US) 1991-11-06 EP disclosed
US-4723030-A ACID CATALYTIC HYDROGENATION OF NITROAROMATIC COMPOUNDS GENERAL ELECTRIC COMPANY (US) 1988-02-02 US disclosed
EP-0212375-A1 Moderated reduction reactions for producing arylhydroxylamines MicroSi, Inc. (a Delaware corporation) (US) 1987-03-04 EP disclosed
EP-0068695-A1 Blends of poly (parabanic acids) with other polymers EXXON RESEARCH AND ENGINEERING COMPANY (US) 1983-01-05 EP disclosed
EP-0057104-A2 Polymers containing 1,3-imidazolidine-1,3-diyl rings plasticized with aromatic sulfones or sulfoxides EXXON RESEARCH AND ENGINEERING COMPANY (US) 1982-08-04 EP disclosed
US-4325860-A Polymers characterized by 1,3-imidazolidine-1,3-diyl rings plasticized with aromatic sulfones or aromatic sulfoxides EXXON RESEARCH & ENGINEERING CO. (US) 1982-04-20 US disclosed