⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL5611758 | 1.00 | — | — | |
| SCHEMBL5611533 | 0.97 | — | — | |
| SCHEMBL5858055 | 0.97 | — | — | |
| SCHEMBL6326957 | 0.97 | — | — | |
| SCHEMBL5927827 | 0.93 | — | — | |
| SCHEMBL9447838 | 0.89 | — | — | |
| SCHEMBL9121618 | 0.89 | — | — | |
| SCHEMBL11018259 | 0.89 | — | — | |
| SCHEMBL8945719 | 0.87 | THRB (0.40) | — | |
| SCHEMBL7906182 | 0.87 | THRB (0.40) | — |
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 5 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1240139-B1 | METHOD FOR PRODUCING N-ALKENYL AMIDES | BASF AG (DE) | 2005-11-09 | — | — | EP | disclosed |
| US-6624303-B2 | By reacting the corresponding NH-amides with acetylenes in the liquid phase using a basic alkali metal compound as catalyst and as cocatalyst (di- or tri-)1,4-butanediol mono- and diethers; N-vinyl-2-pyrrolidone from pyrrolidone | BASF AKTIENGESELLSCHAFT (DE) | 2003-09-23 | — | — | US | disclosed |
| EP-1268380-B1 | METHOD FOR PRODUCING ALKENYL ETHERS | BASF AG (DE) | 2003-09-17 | — | — | EP | disclosed |
| US-20030114715-A1 | Method for producing alkenyl ethers | BOETTCHER ARND (DE) | 2003-06-19 | — | — | US | disclosed |
| US-20030028035-A1 | Method for producing n-alkenyl amides | BASF AKTIENGESELLSCHAFT (DE) | 2003-02-06 | — | — | US | disclosed |