Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KDM4E | B2RXH2 | 8/20 | 0.82 |
| ▸ | LMNA | P02545 | 3/20 | 0.82 |
| ▸ | CCR1 | P32246 | 3/20 | 0.82 |
| ▸ | CCR5 | P51681 | 3/20 | 0.82 |
| ▸ | CCR8 | P51685 | 3/20 | 0.82 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.82 |
| ▸ | POLB | P06746 | 1/20 | 0.82 |
| ▸ | METAP1 | P53582 | 1/20 | 0.82 |
| ▸ | BLM | P54132 | 1/20 | 0.82 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.82 |
| ▸ | DOHH | Q9BU89 | 1/20 | 0.82 |
| ▸ | P4HTM | Q9NXG6 | 1/20 | 0.82 |
| ▸ | NPC1 | O15118 | 6/20 | 0.67 |
| ▸ | RAB9A | P51151 | 5/20 | 0.67 |
| ▸ | TP53 | P04637 | 4/20 | 0.67 |
| ▸ | ALOX15 | P16050 | 3/20 | 0.67 |
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.67 |
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 0.67 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.67 |
| ▸ | HTT | P42858 | 2/20 | 0.67 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Dipyridyl SCHEMBL1982177 | 0.91 | KDM4E (0.88) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL29907716 | 0.91 | KDM4E (1.00) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL29351528 | 0.91 | KDM4E (1.00) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL5922 | 0.91 | KDM4E (1.00) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL3711450 | 0.91 | KDM4E (1.00) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL702299 | 0.88 | KDM4E (0.82) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL708023 | 0.88 | KDM4E (0.82) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL27940432 | 0.88 | KDM4E (0.82) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL6394856 | 0.88 | KDM4E (0.82) | KDM4ELMNACCR1CCR5CCR8 | |
| Dipyridyl SCHEMBL5147238 | 0.88 | KDM4E (0.93) | KDM4ELMNACCR1CCR5CCR8 |
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 106 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8729219-B2 | Polyarylene block copolymer having sulfonic acid group and use thereof | JSR CORPORATION (JP) | 2014-05-20 | — | — | US | disclosed |
| US-20130085236-A1 | POLYARYLENE BLOCK COPOLYMER HAVING SULFONIC ACID GROUP AND USE THEREOF | JSR CORPORATION (JP) | 2013-04-04 | — | — | US | disclosed |
| US-8273499-B2 | Membrane-electrode assembly for solid polymer electrolyte fuel cell | HONDA MOTOR CO., LTD. (JP) | 2012-09-25 | — | — | US | disclosed |
| EP-2112133-B1 | Halogenated aromatic compound, polymer thereof, and proton-conductive membrane comprising same | JSR CORP (JP) | 2012-07-04 | — | — | EP | disclosed |
| EP-1693405-B1 | PROTON CONDUCTING MEMBRANE AND PROCESS FOR PRODUCING THE SAME | JSR CORP (JP) | 2012-05-02 | — | — | EP | disclosed |
| US-20120052412-A1 | POLYARYLENE BLOCK COPOLYMER HAVING SULFONIC ACID GROUP AND USE THEREOF | HONDA MOTOR CO., LTD. (JP) | 2012-03-01 | — | — | US | disclosed |
| EP-2424018-A1 | Polyarylene block copolymer having sulfonic acid group and use thereof | JSR Corporation (JP) | 2012-02-29 | — | — | EP | disclosed |
| US-8058365-B2 | Proton conducting membrane and process for producing the same | JSR CORPORATION (JP) | 2011-11-15 | — | — | US | disclosed |
| US-8039165-B2 | Proton conductive membrane comprising a copolymer | JSR CORPORATION (JP) | 2011-10-18 | — | — | US | disclosed |
| EP-1329444-B1 | Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same | JSR CORP (JP) | 2010-05-05 | — | — | EP | disclosed |
| EP-0601832-B1 | Alkaline ion-absorbing/desorbing carbon material, electrode material for secondary battery using the carbon material and lithium battery using the electrode material | HONDA MOTOR CO LTD (JP) | 1999-05-19 | — | — | EP | disclosed |
| EP-0842208-A1 | 2,7-ARYL-9-SUBSTITUTED FLUORENES AND 9-SUBSTITUTED FLUORENE OLIGOMERS AND POLYMERS | THE DOW CHEMICAL COMPANY (US) | 1998-05-20 | — | — | EP | disclosed |
| US-5728801-A | FILMS USEFUL AS CHARGE TRANSPORT LAYERS IN LIGHT-EMITTING DIODES | THE DOW CHEMICAL COMPANY (US) | 1998-03-17 | — | — | US | disclosed |
| US-5725968-A | Alkaline ion-absorbing/desorbing carbon material electrode material for secondary battery using the carbon material and lithium secondary battery using the electron material | HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) | 1998-03-10 | — | — | US | disclosed |
| EP-0827366-A2 | Heat-resistant organic electroluminescent device | Hewlett-Packard Company (US) | 1998-03-04 | — | — | EP | disclosed |
| WO-1998006773-A1 | POLY(ARYLAMINES) AND FILMS THEREOF | THE DOW CHEMICAL COMPANY (US) | 1998-02-19 | — | — | WO | disclosed |
| US-5708130-A | 2,7-aryl-9-substituted fluorenes and 9-substituted fluorene oligomers and polymers | THE DOW CHEMICAL COMPANY (US) | 1998-01-13 | — | — | US | disclosed |
| WO-1997033193-A2 | CROSS-LINKABLE OR CHAIN EXTENDABLE POLYARYLPOLYAMINES AND FILMS THEREOF | THE DOW CHEMICAL COMPANY (US) | 1997-09-12 | — | — | WO | disclosed |
| WO-1997005184-A1 | 2,7-ARYL-9-SUBSTITUTED FLUORENES AND 9-SUBSTITUTED FLUORENE OLIGOMERS AND POLYMERS | THE DOW CHEMICAL COMPANY (US) | 1997-02-13 | — | — | WO | disclosed |
| EP-0601832-A1 | Alkaline ion-absorbing/desorbing carbon material, electrode material for secondary battery using the carbon material and lithium battery using the electrode material | HONDA GIKEN KOGYO KABUSHIKI KAISHA (JP) | 1994-06-15 | — | — | EP | disclosed |