⚠ 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 | |
|---|---|---|---|---|
| Ammonia Solution, Strong SCHEMBL165122 | 1.00 | — | — | |
| Ammonia Solution, Strong SCHEMBL28334356 | 0.87 | — | — | |
| Phosphine SCHEMBL3166267 | 0.82 | — | — | |
| Ammonia Solution, Strong SCHEMBL3797560 | 0.82 | — | — | |
| Phosphine SCHEMBL188146 | 0.82 | — | — | |
| Ammonia Solution, Strong SCHEMBL6248196 | 0.82 | — | — | |
| Ammonia Solution, Strong SCHEMBL907559 | 0.82 | — | — | |
| Phosphine SCHEMBL15525085 | 0.82 | — | — | |
| Ammonia Solution, Strong SCHEMBL887056 | 0.82 | — | — | |
| Ammonia Solution, Strong SCHEMBL15557146 | 0.82 | — | — |
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 10 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1661903-B1 | NOVEL TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL WITH THE COMPLEX | TAKASAGO PERFUMERY CO LTD (JP) | 2011-05-11 | — | — | EP | claimed |
| US-7473793-B2 | Transition metal (rhodium or ruthenium) complex of a bis(diaryl- or dialicyclylphosphinoaryl) compound and an optionally substituted 1,2-diphenylethylenediamine; hydrogenation catalysts for forming an assymetric alcohol from an assymetric ketone; high optical purity and high yield | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2009-01-06 | — | — | US | claimed |
| US-20060142603-A1 | Transition metal (rhodium or ruthenium) complex of a bis(diaryl- or dialicyclylphosphinoaryl) compound and an optionally substituted 1,2-diphenylethylenediamine; hydrogenation catalysts for forming an assymetric alcohol from an assymetric ketone; high optical purity and high yield | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2006-06-29 | — | — | US | claimed |
| EP-1661903-A1 | NOVEL TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL WITH THE COMPLEX | Takasago International Corporation (JP) | 2006-05-31 | — | — | EP | claimed |
| CN-102060877-B | Transition metal complex containing bidentate nitrogenous ligand, synthetic method and application thereof | SHANGHAI INST ORGANIC CHEM | 2014-07-23 | — | — | CN | disclosed |
| CN-102060877-A | Transition metal complex containing bidentate nitrogenous ligand, synthetic method and application thereof | SHANGHAI INST ORGANIC CHEM | 2011-05-18 | — | — | CN | disclosed |
| EP-1661903-B1 | NOVEL TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL WITH THE COMPLEX | TAKASAGO PERFUMERY CO LTD (JP) | 2011-05-11 | — | — | EP | disclosed |
| US-7473793-B2 | Transition metal (rhodium or ruthenium) complex of a bis(diaryl- or dialicyclylphosphinoaryl) compound and an optionally substituted 1,2-diphenylethylenediamine; hydrogenation catalysts for forming an assymetric alcohol from an assymetric ketone; high optical purity and high yield | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2009-01-06 | — | — | US | disclosed |
| US-20060142603-A1 | Transition metal (rhodium or ruthenium) complex of a bis(diaryl- or dialicyclylphosphinoaryl) compound and an optionally substituted 1,2-diphenylethylenediamine; hydrogenation catalysts for forming an assymetric alcohol from an assymetric ketone; high optical purity and high yield | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2006-06-29 | — | — | US | disclosed |
| EP-1661903-A1 | NOVEL TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING OPTICALLY ACTIVE ALCOHOL WITH THE COMPLEX | Takasago International Corporation (JP) | 2006-05-31 | — | — | EP | disclosed |