⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| SCHEMBL14657732 | 0.82 | — | — | |
| SCHEMBL665724 | 0.65 | — | — | |
| SCHEMBL9059716 | 0.50 | — | — | |
| SCHEMBL4267875 | 0.50 | ALDH1A1 (0.34) | — | |
| SCHEMBL666803 | 0.49 | — | — | |
| SCHEMBL25430945 | 0.46 | — | — | |
| SCHEMBL10017669 | 0.45 | — | — | |
| SCHEMBL262312 | 0.43 | — | — | |
| SCHEMBL179721 | 0.39 | — | — | |
| SCHEMBL2336751 | 0.39 | — | — |
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 50 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117580799-A | Hydrogen storage based on aqueous formate-bicarbonate (bicarbonate) balance | 乔迈斯计划有限责任公司 | 2024-02-20 | — | — | CN | claimed |
| US-8877977-B2 | Synthesis of polyalkylenepolyamines having a low color index by homogeneously catalyzed alcohol amination in the presence of hydrogen | BASF SE (DE) | 2014-11-04 | — | — | US | claimed |
| EP-2782949-A1 | SYNTHESIS OF POLYALKYLENE POLYAMINES WITH LOW COLOR INDEX BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION IN THE PRESENCE OF HYDROGEN | BASF SE (DE) | 2014-10-01 | — | — | EP | claimed |
| US-20130137901-A1 | SYNTHESIS OF POLYALKYLENEPOLYAMINES HAVING A LOW COLOR INDEX BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION IN THE PRESENCE OF HYDROGEN | BASF SE (DE) | 2013-05-30 | — | — | US | claimed |
| WO-2013076053-A1 | SYNTHESIS OF POLYALKYLENE POLYAMINES WITH LOW COLOR INDEX BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION IN THE PRESENCE OF HYDROGEN | BASF SE (DE) | 2013-05-30 | — | — | WO | claimed |
| US-12012426-B2 | Tetradentate diaminodiphosphine ligand and transition metal complex, and method for manufacturing same and application for same | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2024-06-18 | — | — | US | disclosed |
| CN-112654630-B | Tetradentate diaminodiphosphine ligands, transition metal complexes, methods for their production and use thereof | 高砂香料工业株式会社 | 2024-05-24 | — | — | CN | disclosed |
| EP-4363370-A1 | HYDROGEN STORAGE BASED ON AQUEOUS FORMATE-BICARBONATE (HYDROGEN CARBONATE) EQUILIBRIUM | GeoMax Project Kft. (HU) | 2024-05-08 | — | — | EP | disclosed |
| CN-117580799-A | Hydrogen storage based on aqueous formate-bicarbonate (bicarbonate) balance | 乔迈斯计划有限责任公司 | 2024-02-20 | — | — | CN | disclosed |
| US-20230219983-A1 | TETRADENTATE DIAMINODIPHOSPHINE LIGAND AND TRANSITION METAL COMPLEX, AND METHOD FOR MANUFACTURING SAME AND APPLICATION FOR SAME | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2023-07-13 | — | — | US | disclosed |
| US-11639362-B2 | Tetradentate diaminodiphosphine ligand and transition metal complex, and method for manufacturing same and application for same | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2023-05-02 | — | — | US | disclosed |
| WO-2023275578-A1 | HYDROGEN STORAGE BASED ON AQUEOUS FORMATE-BICARBONATE (HYDROGEN CARBONATE) EQUILIBRIUM | GEOMAX PROJECT KFT. (HU) | 2023-01-05 | — | — | WO | disclosed |
| US-20130137901-A1 | SYNTHESIS OF POLYALKYLENEPOLYAMINES HAVING A LOW COLOR INDEX BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION IN THE PRESENCE OF HYDROGEN | BASF SE (DE) | 2013-05-30 | — | — | US | disclosed |
| WO-2013076024-A1 | ALKOXYLATED POLYALKYLENE POLYAMINES | BASF SE (DE) | 2013-05-30 | — | — | WO | disclosed |
| WO-2013076053-A1 | SYNTHESIS OF POLYALKYLENE POLYAMINES WITH LOW COLOR INDEX BY HOMOGENEOUSLY CATALYZED ALCOHOL AMINATION IN THE PRESENCE OF HYDROGEN | BASF SE (DE) | 2013-05-30 | — | — | WO | disclosed |
| US-7501522-B2 | Method for the production of purified 1,3-substituted imidazolium salts | BASF AKTIENGESELLSCHAFT (DE) | 2009-03-10 | — | — | US | disclosed |
| EP-1651614-B1 | METHOD FOR THE PRODUCTION OF PURIFIED 1,3-SUBSTITUTED IMIDAZOLIUM SALTS | BASF AG (DE) | 2007-07-11 | — | — | EP | disclosed |
| US-20060149074-A1 | Method for the production of purified 1,3-substituted imidazolium salts | BASF AKTIENGESELLSCHAFT (DE) | 2006-07-06 | — | — | US | disclosed |
| EP-1651614-A1 | METHOD FOR THE PRODUCTION OF PURIFIED 1,3-SUBSTITUTED IMIDAZOLIUM SALTS | BASF AKTIENGESELLSCHAFT (DE) | 2006-05-03 | — | — | EP | disclosed |
| WO-2005019183-A1 | METHOD FOR THE PRODUCTION OF PURIFIED 1,3-SUBSTITUTED IMIDAZOLIUM SALTS | BASF AKTIENGESELLSCHAFT (DE) | 2005-03-03 | — | — | WO | disclosed |