SCHEMBL3672093

SCHEMBL3672093

CS(=O)(=O)Oc1ccc(-c2ccc(Oc3ccc(-c4ccc(OS(C)(=O)=O)cc4)cc3)cc2)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 7/20 0.53
CA12 O43570 2/20 0.53
MMP2 P08253 2/20 0.50
MMP7 P09237 2/20 0.50
MMP9 P14780 2/20 0.50
MMP14 P50281 2/20 0.50
MMP3 P08254 1/20 0.50
MMP8 P22894 1/20 0.50
CA9 Q16790 5/20 0.45
CA1 P00915 4/20 0.45
MMP1 P03956 1/20 0.42
ALDH1A1 P00352 4/20 0.42
HTT P42858 3/20 0.42
LMNA P02545 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
PGR P06401 1/20 0.41
KDM4E B2RXH2 1/20 0.41
GAA P10253 1/20 0.41
KIF11 P52732 1/20 0.40
ENPP3 O14638 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
SCHEMBL3838977 0.93 CA2 (0.58) CA2CA12MMP2MMP7MMP9
Biphenyl SCHEMBL7191507 0.90 CA2 (0.55) CA2CA12MMP2MMP7MMP9
SCHEMBL9541123 0.86 CA2 (0.57) CA2CA12MMP2MMP7MMP9
SCHEMBL3669919 0.86 CA2 (0.54) CA2CA12MMP2MMP7MMP9
SCHEMBL575589 0.85 CA2 (0.52) CA2CA12MMP2MMP7MMP9
SCHEMBL5700077 0.84 CA2 (0.57) CA2CA12MMP2MMP7MMP9
SCHEMBL2058243 0.84 CA2 (0.64) CA2CA12MMP2MMP7MMP9
SCHEMBL4665445 0.84 CA2 (0.57) CA2CA12CA9CA1ALDH1A1
SCHEMBL3671006 0.83 CA2 (0.51) CA2CA12CA9CA1ALDH1A1
SCHEMBL3675391 0.83 HTT (0.56) CA2MMP2MMP7MMP9MMP14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1329444-B1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR CORP (JP) 2010-05-05 EP disclosed
EP-1138712-B1 Polyarylene copolymers and proton-conductive membrane JSR CORP (JP) 2006-01-18 EP disclosed
US-6933068-B2 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) 2005-08-23 US disclosed
US-6833426-B2 A proton-conductive membrane containing the sulfonic acid group-containing polyarylene (co)polymer JSR CORPORATION (JP) 2004-12-21 US disclosed
US-6812290-B2 FOR USE AS ELECTROLYTES JSR CORPORATION (JP) 2004-11-02 US disclosed
US-20030195301-A1 Polyarylene copolymers and proton-conductive membrane JSR CORPORATION (JP) 2003-10-16 US disclosed
US-20030173547-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR CORPORATION (JP) 2003-09-18 US disclosed
EP-1329444-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR Corporation (JP) 2003-07-23 EP disclosed
US-6555626-B2 Controlled amount of sulfonic acid groups; copolymer of an aromatic compound having a main chain containing electron withdrawing groups and aromatic compounds with no electron withdrawing groups; durability, strength, conductivity JSR CORPORATION (JP) 2003-04-29 US disclosed
US-20020172850-A1 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA, JSR CORPORATION 2002-11-21 US disclosed
US-20010037000-A1 Polyarylene copolymers and proton-conductive membrane JSR CORPORATION (JP) 2001-11-01 US disclosed
EP-1138712-A2 Polyarylene copolymers and proton-conductive membrane JSR Corporation (JP) 2001-10-04 EP disclosed