Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CES2 | O00748 | 1/20 | 0.43 |
| ▸ | CES1 | P23141 | 1/20 | 0.43 |
| ▸ | GSK3B | P49841 | 1/20 | 0.41 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.36 |
| ▸ | LMNA | P02545 | 1/20 | 0.36 |
| ▸ | TMIGD3 | P0DMS9 | 2/20 | 0.35 |
| ▸ | ADORA2A | P29274 | 1/20 | 0.35 |
| ▸ | ADORA1 | P30542 | 1/20 | 0.35 |
| ▸ | MAOB | P27338 | 1/20 | 0.35 |
| ▸ | PGR | P06401 | 1/20 | 0.34 |
| ▸ | TDP2 | O95551 | 1/20 | 0.33 |
| ▸ | MAPK13 | O15264 | 1/20 | 0.32 |
| ▸ | GCGR | P47871 | 1/20 | 0.32 |
| ▸ | MAPK12 | P53778 | 1/20 | 0.32 |
| ▸ | MAPK11 | Q15759 | 1/20 | 0.32 |
| ▸ | MAPK14 | Q16539 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| SCHEMBL3907230 | 0.76 | AR (0.44) | ALDH1A1TMIGD3PGR | |
| SCHEMBL4474410 | 0.74 | MAPK13 (0.48) | GSK3BALDH1A1LMNAPGRMAPK13 | |
| SCHEMBL4590721 | 0.72 | MAPK14 (0.50) | ALDH1A1TMIGD3PGRMAPK13GCGR | |
| SCHEMBL422305 | 0.71 | — | — | |
| SCHEMBL2016588 | 0.71 | CES2 (0.43) | CES2CES1GSK3BALDH1A1LMNA | |
| SCHEMBL18724191 | 0.71 | MAPT (0.53) | ALDH1A1LMNA | |
| SCHEMBL8502740 | 0.67 | — | — | |
| SCHEMBL8303739 | 0.67 | — | — | |
| SCHEMBL612301 | 0.67 | — | — | |
| SCHEMBL11495793 | 0.67 | — | — |
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 45 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0918766-B1 | SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIV MONTREAL (CA) | 2002-02-06 | — | — | EP | claimed |
| US-6051679-A | A META-ALKYLSULFONATE OR META-ALKYLSULFONIC ACID MONOMER CONTAINING POLYTHIOPHENE; POLYMERIZED BY OXIDATIVE DOPING OF THE MONOMER | UNIVERSITEDE MONTREAL (CA) | 2000-04-18 | — | — | US | claimed |
| EP-0918766-A1 | NOVEL SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIVERSITE DE MONTREAL (CA) | 1999-06-02 | — | — | EP | claimed |
| WO-1998003499-A1 | NOVEL SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIVERSITE DE MONTREAL (CA) | 1998-01-29 | — | — | WO | claimed |
| US-12202954-B2 | Rubber composition and crosslinked rubber molded product | SUMITOMO RUBBER INDUSTRIES, LTD. (JP) | 2025-01-21 | — | — | US | disclosed |
| EP-2435497-B1 | POLYCYCLIC DITHIOPHENES | CLAP CO LTD (KR) | 2023-07-05 | — | — | EP | disclosed |
| US-20230114853-A1 | RUBBER COMPOSITION AND CROSSLINKED RUBBER MOLDED PRODUCT | SUMITOMO RUBBER INDUSTRIES, LTD. (JP) | 2023-04-13 | — | — | US | disclosed |
| CN-109790079-B | C (sp) of organozinc reagents and heterocyclic (pseudo) halides3)-C(sp2) Cross-coupling reaction | 香港科技大学 | 2022-06-03 | — | — | CN | disclosed |
| EP-2435500-B1 | DIKETOPYRROLOPYRROLE POLYMERS FOR USE IN ORGANIC SEMICONDUCTOR DEVICES | BASF SE (DE) | 2019-10-30 | — | — | EP | disclosed |
| US-10411292-B2 | All solid state secondary battery, solid electrolyte composition used therefor, electrode sheet for battery, and method for manufacturing electrode sheet for battery and all solid state secondary battery | FUJIFILM CORPORATION (JP) | 2019-09-10 | — | — | US | disclosed |
| EP-3258530-B1 | ALL-SOLID STATE SECONDARY BATTERY, SOLID ELECTROLYTE COMPOSITION USED THEREFOR, ELECTRODE SHEET FOR BATTERY, AND METHODS FOR MANUFACTURING ELECTRODE SHEET FOR BATTERY AND ALL-SOLID STATE SECONDARY BATTERY | FUJIFILM CORP (JP) | 2019-06-19 | — | — | EP | disclosed |
| CN-106432726-B | A kind of lithium-sulphur cell positive electrode high sulfur content polymer and preparation method | 天津大学 | 2019-01-15 | — | — | CN | disclosed |
| US-20100292433-A1 | SOLUBLE POLYTHIOPHENE DERIVATIVE | INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) | 2010-11-18 | — | — | US | disclosed |
| US-20100292433-A1 | SOLUBLE POLYTHIOPHENE DERIVATIVE | INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) | 2010-11-18 | — | — | US | disclosed |
| WO-2009115413-A2 | SUBSTITUTED OLIGO- OR POLYTHIOPHENES | BASF SE (DE) | 2009-09-24 | — | — | WO | disclosed |
| WO-2009115413-A2 | SUBSTITUTED OLIGO- OR POLYTHIOPHENES | BASF SE (DE) | 2009-09-24 | — | — | WO | disclosed |
| EP-0918766-B1 | SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIV MONTREAL (CA) | 2002-02-06 | — | — | EP | disclosed |
| US-6051679-A | A META-ALKYLSULFONATE OR META-ALKYLSULFONIC ACID MONOMER CONTAINING POLYTHIOPHENE; POLYMERIZED BY OXIDATIVE DOPING OF THE MONOMER | UNIVERSITEDE MONTREAL (CA) | 2000-04-18 | — | — | US | disclosed |
| EP-0918766-A1 | NOVEL SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIVERSITE DE MONTREAL (CA) | 1999-06-02 | — | — | EP | disclosed |
| WO-1998003499-A1 | NOVEL SELF-ACID-DOPED HIGHLY CONDUCTING POLYTHIOPHENES | UNIVERSITE DE MONTREAL (CA) | 1998-01-29 | — | — | WO | disclosed |