Sugi Predict

Sugi Predict / Compounds / SCHEMBL610759

SCHEMBL610759

SCHEMBL610759

O=C(c1ccc(F)cc1)c1cc(Cl)ccc1Cl

nearest known ligand 0.53

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.53
▸ TP53 P04637 2/20 0.53
▸ MAPT P10636 4/20 0.52
▸ LMNA P02545 2/20 0.52
▸ HTT P42858 1/20 0.52
▸ KMT2A Q03164 1/20 0.52
▸ SRD5A2 P31213 2/20 0.51
▸ RAB9A P51151 1/20 0.47
▸ KCNMA1 Q12791 1/20 0.46
▸ P2RX1 P51575 1/20 0.46
▸ ERCC5 P28715 1/20 0.44
▸ FEN1 P39748 1/20 0.44
▸ RECQL P46063 1/20 0.44
▸ NR4A1 P22736 1/20 0.43
▸ FLT1 P17948 1/20 0.43
▸ FLT4 P35916 1/20 0.43
▸ KDR P35968 1/20 0.43
▸ LTA4H P09960 1/20 0.43

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
SCHEMBL3677004 0.89 MAPT (0.50) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL7466437 0.89 ALDH1A1 (0.61) ALDH1A1TP53MAPTLMNAKMT2A
SCHEMBL611648 0.86 SRD5A2 (0.70) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL14419294 0.84 P2RX1 (0.60) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL612249 0.84 MAPK1 (0.62) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL2638961 0.83 LTA4H (0.41) TP53MAPTLMNAHTTKMT2A
SCHEMBL2472942 0.83 RECQL (0.57) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL2637828 0.83 ALDH1A1 (0.50) ALDH1A1TP53MAPTLMNARECQL
SCHEMBL18196076 0.83 LMNA (0.50) ALDH1A1TP53MAPTLMNAHTT
SCHEMBL29740498 0.83 ALDH1A1 (0.50) ALDH1A1TP53MAPTLMNARECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9975995-B2 Ion conducting polymer comprising partially branched block copolymer and use thereof KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2018-05-22 — — US disclosed
EP-2206547-B1 NITROGEN-CONTAINING AROMATIC COMPOUNDS AND PROCESSES FOR THE PRODUCTION OF THE SAME, POLYMERS AND PROTON CONDUCTIVE MEMBRANES OF THESE COMPOUNDS JSR CORP (JP) 2016-03-16 — — EP disclosed
US-20150322578-A1 METHOD FOR MANUFACTURING MEMBRANE-ELECTRODE ASSEMBLY, MEMBRANE-ELECTRODE ASSEMBLY, LAMINATE FOR FORMING MEMBRANE-ELECTRODE ASSEMBLY, POLYMER ELECTROLYTE FUEL CELL AND WATER-ELECTROLYSIS DEVICE JSR CORPORATION (JP) 2015-11-12 — — US disclosed
US-20150307659-A1 ION CONDUCTING POLYMER COMPRISING PARTIALLY BRANCHED BLOCK COPOLYMER AND USE THEREOF KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2015-10-29 — — US disclosed
EP-2927998-A1 MEMBRANE-ELECTRODE-ASSEMBLY MANUFACTURING METHOD, MEMBRANE ELECTRODE ASSEMBLY, MEMBRANE-ELECTRODE-ASSEMBLY-FORMING LAMINATES, PROTON EXCHANGE MEMBRANE FUEL CELL, AND WATER-ELECTROLYSIS DEVICE JSR Corporation (JP) 2015-10-07 — — EP disclosed
US-20140154610-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND USES THEREOF JSR CORPORATION (JP) 2014-06-05 — — US disclosed
US-20140154610-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND USES THEREOF JSR CORPORATION (JP) 2014-06-05 — — US disclosed
US-20140154610-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND USES THEREOF JSR CORPORATION (JP) 2014-06-05 — — US disclosed
EP-2738194-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND APPLICATION THEREOF JSR Corporation (JP) 2014-06-04 — — EP disclosed
EP-2738194-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND APPLICATION THEREOF JSR Corporation (JP) 2014-06-04 — — EP disclosed
US-7163988-B2 Aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR CORPORATION (JP) 2007-01-16 — — US disclosed
EP-1245554-B1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR CORP (JP) 2005-01-26 — — EP disclosed
US-6825310-B2 POLYETHER KETONE POLYMERS PROVIDE STABLE MECHANICAL AND THERMAL PROPERTIES (DURABILITY) WHEN SULFONATED; FOR USE IN BATTERIES/FUEL CELLS JSR CORPORATION (JP) 2004-11-30 — — US disclosed
US-6794480-B2 POLYARYLENE-BASED COPOLYMER USEFUL AS PROTON-CONDUCTIVE MEMBRANE WHICH CAN BE USED AS ELECTRON FOR PRIMARY BATTERY, ELECTROLYTE FOR SECONDARY BATTERY, HIGH MOLECULAR SOLID ELECTROLYTE FOR FUEL CELL JSR CORPORATION (JP) 2004-09-21 — — US disclosed
EP-1400548-A1 Novel aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR Corporation (JP) 2004-03-24 — — EP disclosed
US-20040044166-A1 Novel aromatic sulfonic acid ester derivative, polyarylene, polyarylene having sulfonic acid group and process for producing the same, and polymer solid electrolyte and proton-conductive membrane JSR CORPORATION (JP) 2004-03-04 — — US 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
US-20020177656-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR CORPORATION (JP) 2002-11-28 — — US disclosed
EP-1245554-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR Corporation (JP) 2002-10-02 — — EP disclosed
EP-1245555-A1 Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same JSR Corporation (JP) 2002-10-02 — — EP disclosed