SCHEMBL3379116

SCHEMBL3379116

O=S(=O)(O)c1ccccc1NCl

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TTR P02766 2/20 0.46
FABP4 P15090 1/20 0.46
CCNA2 P20248 1/20 0.46
CDK2 P24941 1/20 0.46
MAPK14 Q16539 1/20 0.46
NR4A1 P22736 1/20 0.45
CA2 P00918 7/20 0.41
CA1 P00915 6/20 0.41
CA9 Q16790 2/20 0.41
CA12 O43570 1/20 0.41
CA6 P23280 1/20 0.41
CA5A P35218 1/20 0.41
CA7 P43166 1/20 0.41
CA5B Q9Y2D0 1/20 0.41
MYC P01106 1/20 0.40
TSHR P16473 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
CHAT P28329 1/20 0.39
SNCA P37840 1/20 0.39
KDM4E B2RXH2 1/20 0.39

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
SCHEMBL10552930 0.83 TTR (0.44) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL8779847 0.80 TTR (0.47) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL35949 0.78 HTR6 (0.60) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL5403732 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL7514455 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL14511497 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL7513876 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL998621 0.78 CA2 (0.67) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL31504547 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14
SCHEMBL31504549 0.78 TTR (0.46) TTRFABP4CCNA2CDK2MAPK14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12443103-B2 Conductive composition and method for manufacturing same, and conductor and method for manufacturing same MITSUBISHI CHEMICAL CORPORATION (JP) 2025-10-14 US disclosed
WO-2024257864-A1 WATER SOLUBLE COMPOSITION, METHOD FOR PRODUCING SAME, CONDUCTIVE COMPOSITION, AND METHOD FOR PRODUCING SAME 三菱ケミカル株式会社 2024-12-19 WO disclosed
US-20240371542-A1 CONDUCTOR, CONDUCTIVE COMPOSITION AND LAMINATE MITSUBISHI CHEMICAL CORPORATION (JP) 2024-11-07 US disclosed
CN-118620412-A Conductive composition, resist coating material, resist, and method for forming resist pattern 三菱化学株式会社 2024-09-10 CN disclosed
US-12073956-B2 Conductor, conductive composition and laminate MITSUBISHI CHEMICAL CORPORATION (JP) 2024-08-27 US disclosed
CN-114945635-B Conductive composition, resist coating material, resist, and method for forming resist pattern 三菱化学株式会社 2024-06-18 CN disclosed
CN-112996856-B Conductive composition and method for producing same, and conductive body and method for producing same 三菱化学株式会社 2024-04-09 CN disclosed
WO-2024058243-A1 MANUFACTURING METHOD FOR CONDUCTIVE FILM, MANUFACTURING METHOD FOR MASK, MANUFACTURING METHOD FOR SEMICONDUCTOR DEVICE, DEFECT EXAMINATION METHOD FOR CONDUCTIVE FILM, AND DEFECT EXAMINATION DEVICE 三菱ケミカル株式会社 2024-03-21 WO disclosed
US-20230168584-A1 CONDUCTIVE POLYMER COMPOSITION, COATED PRODUCT, AND PATTERNING PROCESS SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-06-01 US disclosed
CN-116178948-A Conductive polymer composition, cover and pattern forming method 信越化学工业株式会社 2023-05-30 CN disclosed
EP-0834885-B1 Method for producing soluble conductive polymers having acidic groups MITSUBISHI RAYON CO (JP) 2002-01-02 EP disclosed
US-5980784-A SUBJECTING TO ELECTROLYTIC POLYMERIZATION AT LEAST ONE COMPOUND SELECTED FROM THE GROUP CONSISTING OF ACIDIC GROUP SUBSTITUTED ANILINES, PYRROLES, THIOPHENES, FURANS, SELENOPHENES, TELLUROPHENES, ISOTHIANAPHTHENES, IN BASE MITSUBISHI RAYON CO., LTD. (JP) 1999-11-09 US disclosed
US-5932144-A ALKOXY GROUP SUBSTITUTED AMINOBENZENESULFONIC ACID, OR SALT THEREOF MITSUBISHI RAYON CO., LTD. (JP) 1999-08-03 US disclosed
EP-0834885-A2 Method for producing soluble conductive polymer having acidic groups NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1998-04-08 EP disclosed
US-5700399-A Soluble alkoxy-group substituted aminobenzenesulfonic acid aniline conducting polymers NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1997-12-23 US disclosed
US-5610298-A Water-soluble anthraquinone compounds, preparation thereof and use thereof as dyes HOECHST AKTIENGESELLSCHAFT (DE) 1997-03-11 US disclosed
US-5589108-A Soluble alkoxy-group substituted aminobenzenesulfonic acid aniline conducting polymers NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1996-12-31 US disclosed
EP-0662694-A2 Soluble aniline conducting polymers NITTO CHEMICAL INDUSTRY CO., LTD. (JP) 1995-07-12 EP disclosed
US-4594411-A Sulfonated monoazo colorant lake obtained by di-azo coupling of 5-acetylamino-2-aminobenzene-1-sulfonic acid with 1-(3'-sulfophenyl)-3-methylphyrazol-5-one BASF AKTIENGESELLSCHAFT (DE) 1986-06-10 US disclosed
EP-0073972-A1 Lake of an azo dyestuff containing sulphonic acid groups BASF Aktiengesellschaft (DE) 1983-03-16 EP disclosed