SCHEMBL3679922

SCHEMBL3679922

O=S(=O)(Oc1cccc(-c2ccc(Oc3cccc(-c4cccc(OS(=O)(=O)C(F)(F)F)c4)c3)cc2)c1)C(F)(F)F

nearest known ligand 0.48

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
FFAR4 Q5NUL3 4/20 0.48
FFAR1 O14842 3/20 0.48
SDHB P21912 1/20 0.45
GSTP1 P09211 1/20 0.45
BCL2L1 Q07817 2/20 0.43
MCL1 Q07820 2/20 0.43
PPARG P37231 1/20 0.42
PTPN1 P18031 2/20 0.42
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
CA9 Q16790 2/20 0.41
SCN9A Q15858 1/20 0.40
NR3C1 P04150 1/20 0.40
PGR P06401 1/20 0.40
AR P10275 1/20 0.40
ESR2 Q92731 1/20 0.40
KCNH2 Q12809 1/20 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
SCHEMBL3670256 0.98 GSTP1 (0.46) FFAR4FFAR1SDHBGSTP1BCL2L1
SCHEMBL3669696 0.97 FFAR4 (0.48) FFAR4FFAR1SDHBGSTP1BCL2L1
Biphenyl SCHEMBL7928872 0.89 PPARG (0.49) SDHBBCL2L1MCL1PPARGPTPN1
SCHEMBL4684800 0.89 PTPN1 (0.47) SDHBPTPN1CA1CA2CA9
SCHEMBL13416088 0.88 CA1 (0.45) SDHBPTPN1CA1CA2CA9
SCHEMBL5179650 0.87 CA1 (0.50) PPARGPTPN1CA1CA2CA9
SCHEMBL27542368 0.86 MRGPRX4 (0.46) PTPN1CA1CA2CA9KCNH2
SCHEMBL5177944 0.85 CA1 (0.50) SDHBPPARGPTPN1CA1CA2
SCHEMBL27517450 0.84 ADORA2A (0.46) PTPN1KCNH2
SCHEMBL27520200 0.84 ALDH1A1 (0.42) PTPN1CA1CA2CA9KCNH2

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