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Sugi Predict / Compounds / SCHEMBL3679848

SCHEMBL3679848

SCHEMBL3679848

O=S(=O)(c1ccc(Oc2ccc(S(=O)(=O)c3cccc(OS(=O)(=O)C(F)(F)F)c3)cc2)cc1)c1cccc(OS(=O)(=O)C(F)(F)F)c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 2/20 0.51
▸ SMN1; SMN2 Q16637 1/20 0.51
▸ L3MBTL1 Q9Y468 2/20 0.50
▸ TDP1 Q9NUW8 1/20 0.50
▸ PGR P06401 7/20 0.45
▸ NR3C1 P04150 1/20 0.45
▸ AR P10275 1/20 0.45
▸ ESR2 Q92731 1/20 0.45
▸ SOS1 Q07889 1/20 0.44
▸ POLB P06746 1/20 0.43
▸ APEX1 P27695 1/20 0.43
▸ CTDSP1 Q9GZU7 1/20 0.43
▸ PTPN1 P18031 1/20 0.43
▸ ABCC9 O60706 1/20 0.43
▸ ABCC8 Q09428 1/20 0.43
▸ KCNJ11 Q14654 1/20 0.43
▸ KCNJ8 Q15842 1/20 0.43
▸ PPARG P37231 1/20 0.41
▸ PTGES2 Q9H7Z7 1/20 0.41
▸ LMNA P02545 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
SCHEMBL3677240 0.98 HTT (0.52) HTTSMN1; SMN2L3MBTL1TDP1PGR
SCHEMBL3672508 0.95 HTT (0.52) HTTSMN1; SMN2L3MBTL1TDP1PGR
SCHEMBL3676366 0.91 F2 (0.43) HTTSMN1; SMN2PGRNR3C1AR
SCHEMBL3671604 0.85 HTT (0.53) HTTSMN1; SMN2L3MBTL1TDP1SOS1
SCHEMBL5179650 0.82 CA1 (0.50) HTTSMN1; SMN2L3MBTL1TDP1PGR
SCHEMBL4150360 0.82 HTR6 (0.54) HTTSMN1; SMN2TDP1SOS1POLB
SCHEMBL11418604 0.82 HTT (0.68) HTTSMN1; SMN2L3MBTL1TDP1PGR
SCHEMBL3675287 0.81 HTT (0.56) HTTSMN1; SMN2L3MBTL1TDP1PGR
SCHEMBL5177944 0.80 CA1 (0.50) SMN1; SMN2PGRNR3C1ARESR2
SCHEMBL3675538 0.80 HTT (0.59) HTTSMN1; SMN2L3MBTL1TDP1PGR

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