SCHEMBL3673494

SCHEMBL3673494

O=S(=O)(c1ccc(Oc2ccc(S(=O)(=O)c3cccc(I)c3)cc2)cc1)c1cccc(I)c1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 7/20 0.53
L3MBTL1 Q9Y468 2/20 0.53
TDP1 Q9NUW8 1/20 0.53
SMN1; SMN2 Q16637 6/20 0.50
POLB P06746 3/20 0.45
APEX1 P27695 1/20 0.45
CTDSP1 Q9GZU7 1/20 0.45
ALDH1A1 P00352 5/20 0.42
PKM P14618 2/20 0.42
SOS1 Q07889 1/20 0.42
LMNA P02545 5/20 0.41
GAA P10253 1/20 0.41
KMT2A Q03164 1/20 0.41
HTR6 P50406 1/20 0.40
MAPT P10636 3/20 0.39
NPC1 O15118 1/20 0.39
TP53 P04637 1/20 0.39
TSHR P16473 1/20 0.39
XBP1 P17861 1/20 0.39
MAPK1 P28482 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
SCHEMBL6058986 0.95 HTT (0.56) HTTL3MBTL1TDP1SMN1; SMN2POLB
SCHEMBL3668530 0.86 HTT (0.58) HTTL3MBTL1TDP1SMN1; SMN2POLB
SCHEMBL30084552 0.84 LMNA (0.54) HTTSMN1; SMN2POLBALDH1A1LMNA
SCHEMBL3677379 0.84 LMNA (0.54) HTTSMN1; SMN2POLBALDH1A1LMNA
SCHEMBL9756893 0.83 HTR6 (0.48) HTTL3MBTL1SMN1; SMN2ALDH1A1LMNA
SCHEMBL3839132 0.83 HTR6 (0.61) HTTSMN1; SMN2POLBALDH1A1LMNA
SCHEMBL11418604 0.81 HTT (0.68) HTTL3MBTL1TDP1SMN1; SMN2POLB
SCHEMBL3669592 0.81 HTT (0.55) HTTL3MBTL1TDP1SMN1; SMN2POLB
SCHEMBL20389273 0.80 HTR6 (0.59) HTTTDP1ALDH1A1PKMLMNA
SCHEMBL3671678 0.79 PGR (0.57) HTTL3MBTL1TDP1SMN1; SMN2POLB

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