⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL5482404 | 0.74 | — | — | |
| SCHEMBL2030787 | 0.74 | — | — | |
| SCHEMBL2025450 | 0.72 | — | — | |
| SCHEMBL8837318 | 0.71 | — | — | |
| SCHEMBL28327789 | 0.69 | — | — | |
| SCHEMBL2022263 | 0.69 | — | — | |
| SCHEMBL332908 | 0.68 | — | — | |
| SCHEMBL16486715 | 0.68 | — | — | |
| SCHEMBL27900280 | 0.66 | — | — | |
| SCHEMBL16115512 | 0.66 | — | — |
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 12 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-111423874-A | Preparation method of organic polymer grafted nano-silica coated quantum dot | 青岛大学 | 2020-07-17 | — | — | CN | claimed |
| CN-111423874-A | Preparation method of organic polymer grafted nano-silica coated quantum dot | 青岛大学 | 2020-07-17 | — | — | CN | disclosed |
| US-8846842-B2 | Production and use of highly functional, highly branched or hyperbranched polylysines | BASF AKTIENGESELLSCHAFT (DE) | 2014-09-30 | — | — | US | disclosed |
| EP-2332969-B1 | Use of highly functional, highly branched or hyperbranched polylysines | BASF SE (DE) | 2013-08-07 | — | — | EP | disclosed |
| US-8378049-B2 | Production and use of highly functional, highly branched or hyperbranched polylysines | BASF AKTIENGESELLSCHAFT (DE) | 2013-02-19 | — | — | US | disclosed |
| EP-2332969-A2 | Production of highly functional, highly branched or hyperbranched polylysines | BASF SE (DE) | 2011-06-15 | — | — | EP | disclosed |
| US-20100249369-A1 | Production and use of highly functional, highly branched or hyperbranched polylysines | BASF SE (DE) | 2010-09-30 | — | — | US | disclosed |
| US-20100222539-A1 | Production and use of highly functional, highly branched or hyperbranched polylysines | BASF SE (DE) | 2010-09-02 | — | — | US | disclosed |
| US-7786240-B2 | Reacting a salt of lysine with at least one acid in the presence of a tertiary amine or amidine, or an organometallic compound; additional reactants may include another amino acid, a di- or polycarboxylic acid, a di- or polyamine or derivative | BASF AKTIENGESELLSCHAFT (DE) | 2010-08-31 | — | — | US | disclosed |
| EP-2194063-A2 | Production and use of modified polylysines | BASF SE (DE) | 2010-06-09 | — | — | EP | disclosed |
| EP-1957519-B1 | PRODUCTION OF HIGHLY FUNCTIONAL, HIGHLY BRANCHED OR HYPERBRANCHED POLYLYSINES | BASF SE (DE) | 2010-05-19 | — | — | EP | disclosed |
| US-20090048416-A1 | Reacting a salt of lysine with at least one acid in the presence of a tertiary amine or amidine, or an organometallic compound; additional reactants may include another amino acid, a di- or polycarboxylic acid, a di- or polyamine or derivative | BASF SE (DE) | 2009-02-19 | — | — | US | disclosed |