⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL8347902 | 0.67 | — | — | |
| SCHEMBL9718493 | 0.65 | — | — | |
| SCHEMBL10767319 | 0.61 | — | — | |
| SCHEMBL435609 | 0.60 | — | — | |
| SCHEMBL10881279 | 0.60 | — | — | |
| SCHEMBL8213246 | 0.57 | — | — | |
| SCHEMBL7106345 | 0.56 | — | — | |
| SCHEMBL16773943 | 0.56 | — | — | |
| Water SCHEMBL2164398 | 0.56 | — | — | |
| Succinchlorimide SCHEMBL72 | 0.54 | — | — |
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 4 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2545032-A1 | PREPARATION OF METHIONINE OR SELENOMETHIONINE FROM HOMOSERINE VIA A LACTONE INTERMEDIATE | Novus International Inc. (US) | 2013-01-16 | — | — | EP | disclosed |
| CN-102869646-A | Method for producing methionine or selenomethionine from homoserine via a lactone intermediate | NOVUS INT INC | 2013-01-09 | — | — | CN | disclosed |
| US-20130006014-A1 | Preparation of Methionine or Selenomethionine from Homoserine via a Lactone Intermediate | NOVUS INTERNATIONAL INC. (US) | 2013-01-03 | — | — | US | disclosed |
| WO-2011112649-A1 | PREPARATION OF METHIONINE OR SELENOMETHIONINE FROM HOMOSERINE VIA A LACTONE INTERMEDIATE | NOVUS INTERNATIONAL INC. (US) | 2011-09-15 | — | — | WO | disclosed |