SCHEMBL6009067

SCHEMBL6009067

O=S(=O)(c1ccc(Cl)cc1)c1cccc(-c2cc(S(=O)(=O)c3ccc(Cl)cc3)ccc2-c2ccccc2)c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.48
CYP3A4 P08684 1/20 0.48
MAPK1 P28482 1/20 0.48
PTGS2 P35354 5/20 0.47
PTGS1 P23219 2/20 0.47
GAA P10253 3/20 0.45
HTT P42858 2/20 0.45
KDM4E B2RXH2 2/20 0.45
LMNA P02545 2/20 0.44
PKM P14618 1/20 0.43
MAPT P10636 3/20 0.43
KMT2A Q03164 2/20 0.43
NFKB1 P19838 1/20 0.43
NFKB2 Q00653 1/20 0.43
RELA Q04206 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
HTR6 P50406 1/20 0.42
MEN1 O00255 1/20 0.42
CYP2C9 P11712 1/20 0.42
HPGD P15428 1/20 0.42

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
SCHEMBL6009061 0.92 PTGS2 (0.56) ALDH1A1CYP3A4MAPK1PTGS2PTGS1
SCHEMBL13731761 0.92 PTGS2 (0.56) ALDH1A1CYP3A4MAPK1PTGS2PTGS1
SCHEMBL13731763 0.91 ALDH1A1 (0.55) ALDH1A1CYP3A4MAPK1PTGS2PTGS1
SCHEMBL11045136 0.83 PTGS2 (0.53) ALDH1A1MAPK1PTGS2PTGS1HTT
SCHEMBL10459473 0.82 ALDH1A1 (0.46) ALDH1A1CYP3A4MAPK1PTGS2PTGS1
SCHEMBL5890635 0.81 ALDH1A1 (0.50) ALDH1A1PTGS2PTGS1
SCHEMBL3006195 0.78 ALDH1A1 (0.73) ALDH1A1CYP3A4MAPK1GAAHTT
SCHEMBL250144 0.78 ALDH1A1 (0.80) ALDH1A1CYP3A4MAPK1GAAHTT
SCHEMBL9766560 0.78 TSHR (0.50) ALDH1A1PTGS2KMT2AMEN1THRB
SCHEMBL2311184 0.78 LRRK2 (0.56) PTGS2PTGS1

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2791094-B1 A PROCESS FOR MANUFACTURING HALOARYL COMPOUNDS FROM MIXTURES OF ISOMERS OF DIHALODIARYLSULFONES SOLVAY SPECIALTY POLYMERS USA (US) 2021-02-17 EP disclosed
EP-2699541-B1 PROCESS FOR THE MANUFACTURE OF DIHALODIPHENYLSULFONES STARTING FROM ORGANIC ACIDS SOLVAY SPECIALTY POLYMERS USA (US) 2017-06-14 EP disclosed
US-9388128-B2 Process for the manufacture of dihalodiphenylsulfones starting from organic acids SOLVAY SPECIALITY POLYMERS USA, LLC (US) 2016-07-12 US disclosed
US-9212111-B2 Process for manufacturing haloaryl compounds from mixtures of isomers of dihalodiarylsulfone SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2015-12-15 US disclosed
US-20140323765-A1 Process for Manufacturing Haloaryl Compounds From Mixtures of Isomers of Dihalodiarylsulfone SOLVAY SPECIALTY POLYMERS USA, LLC. (US) 2014-10-30 US disclosed
EP-2791094-A1 A PROCESS FOR MANUFACTURING HALOARYL COMPOUNDS FROM MIXTURES OF ISOMERS OF DIHALODIARYLSULFONES Solvay Specialty Polymers USA, LLC. (US) 2014-10-22 EP disclosed
US-20140228597-A1 Process for the manufacture of dihalodiphenylsulfones starting from organic acids SOLVAY SPECIALITY POLYMERS USA, LLC (US) 2014-08-14 US disclosed
EP-2699541-A1 PROCESS FOR THE MANUFACTURE OF DIHALODIPHENYLSULFONES STARTING FROM ORGANIC ACIDS Solvay Specialty Polymers USA, LLC. (US) 2014-02-26 EP disclosed
WO-2013087594-A1 A PROCESS FOR MANUFACTURING HALOARYL COMPOUNDS FROM MIXTURES OF ISOMERS OF DIHALODIARYLSULFONES SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2013-06-20 WO disclosed
WO-2012143279-A1 PROCESS FOR THE MANUFACTURE OF DIHALODIPHENYLSULFONES STARTING FROM ORGANIC ACIDS SOLVAY SPECIALTY POLYMERS USA, LLC (US) 2012-10-26 WO disclosed
EP-1112301-B1 ION-EXCHANGE POLYMERS VICTREX MFG LTD (GB) 2006-09-06 EP disclosed
US-6969755-B2 polyether ketone and/or sulfone copolymers having chemical resistance, used as polyelectrolyte membranes for fuel cells VICTREX MANUFACTURING LIMITED (GB) 2005-11-29 US disclosed
EP-1493770-A2 Ion-exchange polymers VICTREX MANUFACTURING LIMITED (GB) 2005-01-05 EP disclosed
US-6828353-B1 Sulphonated polyaryletherketones, polyarylethersulphones and/or copolymers of VICTREX MANUFACTURING LIMITED (GB) 2004-12-07 US disclosed
US-20040242710-A1 Ion-exchange polymers VICTREX MANUFACTURING LIMITED (GB) 2004-12-02 US disclosed
EP-0278720-B1 Aromatic polymer VICTREX MFG LTD (GB) 1995-01-18 EP disclosed
US-5116933-A Crystalline IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1992-05-26 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 (2 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-20140323765-A1 Process for Manufacturing Haloaryl Compounds From Mixtures of Isomers of Dihalodiarylsulfone HDHD5, DHCR7, DDT ALDH1A1 303/4885CYP3A4 61/4885MAPK1 2512/4885
US-20140228597-A1 Process for the manufacture of dihalodiphenylsulfones starting from organic acids DDT, CYP2B6, HPD ALDH1A1 669/4885CYP3A4 8/4885MAPK1 2513/4885

“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.