Sugi Predict

Sugi Predict / Compounds / SCHEMBL809347

SCHEMBL809347

SCHEMBL809347

O=C(c1ccc(Cl)cc1)c1ccc(Oc2ccc(S(=O)(=O)c3ccc(Oc4ccc(C(=O)c5ccc(Cl)cc5)cc4)cc3)cc2)cc1

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HPGD P15428 1/20 0.56
▸ MAPK1 P28482 2/20 0.55
▸ ALDH1A1 P00352 1/20 0.55
▸ CYP3A4 P08684 1/20 0.55
▸ POLB P06746 2/20 0.51
▸ APEX1 P27695 1/20 0.51
▸ CTDSP1 Q9GZU7 1/20 0.51
▸ L3MBTL1 Q9Y468 1/20 0.51
▸ MMP1 P03956 2/20 0.49
▸ ELANE P08246 1/20 0.49
▸ MAPT P10636 1/20 0.49
▸ PKM P14618 1/20 0.49
▸ SRD5A2 P31213 2/20 0.48
▸ FABP2 P12104 1/20 0.47
▸ PPARG P37231 1/20 0.47
▸ PPARA Q07869 1/20 0.47
▸ SLC22A12 Q96S37 1/20 0.47
▸ MEN1 O00255 1/20 0.47
▸ KMT2A Q03164 1/20 0.47
▸ PRMT1 Q99873 1/20 0.47

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
SCHEMBL822929 1.00 HPGD (0.56) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL12960262 1.00 HPGD (0.56) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL12960261 1.00 HPGD (0.56) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL17207952 1.00 HPGD (0.56) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL17207958 0.95 HPGD (0.51) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL17209197 0.94 MAPK1 (0.61) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL17209192 0.90 HPGD (0.50) HPGDMAPK1ALDH1A1CYP3A4POLB
SCHEMBL5527337 0.89 MAPK1 (0.70) HPGDMAPK1ALDH1A1CYP3A4MAPT
SCHEMBL9475034 0.89 MAPK1 (0.70) HPGDMAPK1ALDH1A1CYP3A4MAPT
SCHEMBL7822703 0.88 POLB (0.66) MAPK1ALDH1A1CYP3A4POLBAPEX1

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 90 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8293905-B2 Bipyridine compound, transition metal complex, and method for production of conjugated aromatic compound using the transition metal complex SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-10-23 — — US disclosed
US-20120251919-A1 POLYARYLENE-BASED COPOLYMER AND USES THEREOF SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-10-04 — — US disclosed
US-8236920-B2 Polyarylene and process for producing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-08-07 — — US disclosed
EP-1693405-B1 PROTON CONDUCTING MEMBRANE AND PROCESS FOR PRODUCING THE SAME JSR CORP (JP) 2012-05-02 — — EP disclosed
US-8088883-B2 Transition metal complex and process for producing conjugated aromatic compound using the transition metal complex SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-01-03 — — US disclosed
EP-1845122-B1 POLYARYLENE, PROCESS FOR PRODUCING THE SAME, SOLID POLYELECTROLYTE, AND PROTON-CONDUCTIVE FILM JSR CORP (JP) 2011-11-16 — — EP disclosed
US-8058365-B2 Proton conducting membrane and process for producing the same JSR CORPORATION (JP) 2011-11-15 — — US disclosed
US-20110275859-A1 METHOD FOR MANUFACTURING CONJUGATED AROMATIC COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED 2011-11-10 — — US disclosed
US-20110275780-A1 METHOD FOR PRODUCING CONJUGATED AROMATIC COMPOUND SUMITOMO CHEMCIAL COMPANY LIMITED 2011-11-10 — — US disclosed
US-8039165-B2 Proton conductive membrane comprising a copolymer JSR CORPORATION (JP) 2011-10-18 — — US disclosed
US-20040043297-A1 Proton conductive resin composition, method for preparing the same, and proton conductive membrane comprising the composition JSR CORPORATION 2004-03-04 — — US disclosed
EP-1391480-A1 Proton conductive resin composition, method for preparing the same, and proton conductive membrane comprising the composition JSR Corporation (JP) 2004-02-25 — — EP disclosed
US-20040028806-A1 Process for producing electrolyte membrane-bonded electrode and varnish composition used therein THE RELIABLE AUTOMATIC SPRINKLER CO. INC. 2004-02-12 — — US disclosed
US-6685984-B2 FORMING FUEL CELL COMPRISED OF NONPENETRATING ELECTROLYTE MEMBRANE ON ELECTRODE JSR CORPORATION (JP) 2004-02-03 — — US disclosed
US-20030228421-A1 Method for the production of multilayers JSR CORPORATION 2003-12-11 — — 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-20020188097-A1 Polyether ketone polymers provide stable mechanical and thermal properties (durability) when sulfonated; for use in batteries/fuel cells JSR CORPORATION (JP) 2002-12-12 — — US disclosed
EP-1245555-A1 Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same JSR Corporation (JP) 2002-10-02 — — EP disclosed
EP-0317226-A2 Aromatic compounds IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-05-24 — — EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110275859-A1 METHOD FOR MANUFACTURING CONJUGATED AROMATIC COMPOUND C9, H1-10, CYP1A1 HPGD 3914/4885MAPK1 1740/4885ALDH1A1 46/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.