SCHEMBL4795650

SCHEMBL4795650

O=C1c2cccc(S(=O)(=O)O)c2C(=O)c2cccc(S(=O)(=O)O)c21.[Na].[Na]

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
STAT3 P40763 1/20 0.56
ALDH1A1 P00352 6/20 0.50
MAOA P21397 5/20 0.50
SMN1; SMN2 Q16637 5/20 0.50
PGAM1 P18669 1/20 0.49
HSD17B10 Q99714 4/20 0.43
MAPT P10636 4/20 0.43
MAPK1 P28482 4/20 0.43
TSHR P16473 3/20 0.43
HPGD P15428 3/20 0.43
ALOX15 P16050 3/20 0.43
LMNA P02545 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
MAOB P27338 1/20 0.43
HTT P42858 1/20 0.43
L3MBTL1 Q9Y468 3/20 0.43
THRB P10828 1/20 0.43
TTR P02766 1/20 0.42
ADORA2A P29274 2/20 0.41
MEN1 O00255 2/20 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
SCHEMBL29490318 1.00 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL3098752 1.00 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL1270794 0.98 STAT3 (0.58) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL2155220 0.96 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL2786333 0.96 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
Water SCHEMBL2155568 0.96 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL2788339 0.96 STAT3 (0.56) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL230644 0.92 ALDH1A1 (0.61) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL29470867 0.92 ALDH1A1 (0.61) STAT3ALDH1A1MAOASMN1; SMN2PGAM1
SCHEMBL2851640 0.92 STAT3 (0.53) STAT3ALDH1A1MAOASMN1; SMN2PGAM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6191318-B1 CONTACTING AROMATIC COMPOUND WITH AT LEAST ONE TWO-COMPONENT HETEROGENEOUS CATALYST COMPRISING AT LEAST ONE ZEOLITE CATALYST WHICH CONTAINS AT LEAST ONE GROUP VIII B TRANSITION METAL AND AT LEAST ONE ALKYL ANTHRAQUINONE OR ITS DERIVATIVE KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2001-02-20 US claimed
US-6165341-A Catalytic film, methods of making the catalytic films, and electrosynthesis of compounds using the catalytic film SACHEM, INC. (US) 2000-12-26 US claimed
EP-1021595-A2 ELECTROSYNTHESIS OF HYDROXYLAMMONIUM SALTS AND HYDROXYLAMINE USING A MEDIATOR, A CATALYTIC FILM, METHODS OF MAKING THE CATALYTIC FILM, AND ELECTROSYNTHESIS OF COMPOUNDS USING THE CATALYTIC FILM SACHEM, INC. (US) 2000-07-26 EP claimed
US-6024855-A Electrosynthesis of hydroxylammonium salts and hydroxylamine using a mediator SACHEM, INC. (US) 2000-02-15 US claimed
WO-1999064129-A2 PROCESS FOR PREPARING HYDROXYLATED AROMATICS BY HYDROGEN AND OXYGEN KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 1999-12-16 WO claimed
US-5972305-A ENCAPSULATING ONE OR MORE TRANSITION METALS OF GROUP VIII OF THE PERIODIC TABLE AND HYDROGEN CARRIER COMPOUNDS ON THE ZEOLITE CHANNELS; SUPPLYING HYDROGEN AND OXYGEN SIMULTANEOUSLY AT A REACTION TEMPERATURE OF 10-90 DEGREES C KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 1999-10-26 US claimed
WO-1999009234-A2 ELECTROSYNTHESIS OF HYDROXYLAMMONIUM SALTS AND HYDROXYLAMINE USING A MEDIATOR, A CATALYTIC FILM, METHODS OF MAKING THE CATALYTIC FILM, AND ELECTROSYNTHESIS OF COMPOUNDS USING THE CATALYTIC FILM SACHEM, INC. (US) 1999-02-25 WO claimed
CN-110649227-A Three-dimensional composite potassium metal cathode and preparation method and application thereof 天津大学 2020-01-03 CN disclosed
EP-2700712-B1 METHOD FOR ELECTROPHORESING NUCLEIC ACIDS, METHOD FOR CONCENTRATING AND PURIFYING NUCLEIC ACIDS, CARTRIDGE FOR NUCLEIC ACID ELECTROPHORESIS, AND METHOD FOR PRODUCING CARTRIDGE FOR NUCLEIC ACID ELECTROPHORESIS SONY CORP (JP) 2016-12-28 EP disclosed
US-20160001237-A1 ASYMMETRICALLY POROUS MEMBRANES MADE OF CROSS-LINKED THERMOPLASTIC SILICONE ELASTOMER WACKER CHEMIE AG (DE) 2016-01-07 US disclosed
EP-1928965-B1 COMPOSITIONS AND METHODS FOR TANTALUM CMP CABOT MICROELECTRONICS CORP (US) 2015-12-30 EP disclosed
CN-105026023-A Asymmetric porous membranes made from crosslinked thermoplastic silicone elastomers WACKER CHEMIE AG 2015-11-04 CN disclosed
EP-2700712-A1 METHOD FOR ELECTROPHORESING NUCLEIC ACIDS, METHOD FOR CONCENTRATING AND PURIFYING NUCLEIC ACIDS, CARTRIDGE FOR NUCLEIC ACID ELECTROPHORESIS, AND METHOD FOR PRODUCING CARTRIDGE FOR NUCLEIC ACID ELECTROPHORESIS Sony Corporation (JP) 2014-02-26 EP disclosed
US-5641850-A HYDROSILATION OF A HYDRIDOPOLYSILOXANE BY AN ALKENE CONTAINING MESOGENIC GROUPS FOLLOWED BY REACTION WITH AN ALKENE CONTAINING A (METH)ACRYLOXY GROUP; CROSSLINKING; HAZE-FREE FILMS CONSORTIUM FUR ELECTROCHEMISCHE INDUSTRIE GMBH (DE) 1997-06-24 US disclosed
US-5593787-A Organosilicon compounds containing (meth) acryloxy groups, their preparation and their use WACKER-CHEMIE GMBH (DE) 1997-01-14 US disclosed
CN-1132753-A Organosilicon compounds containing (meth) acryloxy groups, their preparation and their use WACKER CHEMIE GMBH (DE) 1996-10-09 CN disclosed
US-5214077-A ORGANOSILICON COMPOUNDS CONTAINING (METH)ACRYLOXY GROUPS, THEIR PREPARATION AND USE WACKER-CHEMIE GMBH (DE) 1993-05-25 US disclosed
EP-0341991-A2 Method for recovery of antibiotics from mother liquors and novel pharmaceutically-acceptable salts thereof ELI LILLY AND COMPANY (US) 1989-11-15 EP disclosed
US-4605567-A PHOTOPOLYMERIZATION OF ALLYL ANHYDRIDE-MODIFIED POLYSILOXANES REACTED WITH HYDROXYETHYL ACRYLATE WACKER-CHEMIE GMBH (DE) 1986-08-12 US disclosed
US-3985741-A Production of p-hydroxycephalexin BRISTOL-MYERS COMPANY (US) 1976-10-12 US disclosed