SCHEMBL3671604

SCHEMBL3671604

O=S(=O)(c1ccc(Oc2ccc(S(=O)(=O)c3ccc(OS(=O)(=O)C(F)(F)F)cc3)cc2)cc1)c1ccc(OS(=O)(=O)C(F)(F)F)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 6/20 0.53
SMN1; SMN2 Q16637 4/20 0.53
PTPN1 P18031 2/20 0.47
ALDH1A1 P00352 4/20 0.45
PKM P14618 2/20 0.45
SOS1 Q07889 2/20 0.44
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
CA9 Q16790 1/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
POLB P06746 2/20 0.44
APEX1 P27695 1/20 0.44
CTDSP1 Q9GZU7 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
HSD11B1 P28845 1/20 0.41
LMNA P02545 4/20 0.41
MAPT P10636 2/20 0.41
NPC1 O15118 1/20 0.41
TP53 P04637 1/20 0.41
TSHR P16473 1/20 0.41

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
SCHEMBL822779 0.94 PKM (0.50) HTTSMN1; SMN2PTPN1ALDH1A1PKM
SCHEMBL5179823 0.90 PTPN1 (0.53) HTTSMN1; SMN2PTPN1ALDH1A1SOS1
SCHEMBL4150360 0.89 HTR6 (0.54) HTTSMN1; SMN2PTPN1ALDH1A1PKM
SCHEMBL3672508 0.87 HTT (0.52) HTTSMN1; SMN2PTPN1SOS1CA1
SCHEMBL3679848 0.85 HTT (0.51) HTTSMN1; SMN2PTPN1SOS1CA1
SCHEMBL28028096 0.85 PKM (0.47) HTTSMN1; SMN2PTPN1ALDH1A1PKM
SCHEMBL19564840 0.85 HTT (0.59) HTTSMN1; SMN2ALDH1A1PKMCA1
SCHEMBL20924560 0.85 PKM (0.68) HTTPKMCA1CA2CA9
SCHEMBL811054 0.85 PKM (0.58) HTTSMN1; SMN2PTPN1ALDH1A1PKM
SCHEMBL3677240 0.84 HTT (0.52) HTTSMN1; SMN2PTPN1SOS1CA1

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