⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL460908 | 0.87 | — | — | |
| Fluoride SCHEMBL22583589 | 0.84 | GLRA1 (0.41) | — | |
| SCHEMBL2373214 | 0.84 | — | — | |
| SCHEMBL7173080 | 0.74 | TERT (0.33) | — | |
| SCHEMBL28827579 | 0.74 | — | — | |
| SCHEMBL28471850 | 0.74 | — | — | |
| SCHEMBL1685402 | 0.73 | — | — | |
| SCHEMBL163295 | 0.73 | — | — | |
| SCHEMBL8779189 | 0.73 | — | — | |
| SCHEMBL27489171 | 0.73 | CRBN (0.43) | — |
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 15 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0413675-B1 | Method for producing synthetic N-linked glycoconjugates | MONSANTO CO (US) | 1995-05-03 | — | — | EP | claimed |
| US-5212298-A | Method for producing synthetic N-linked glycoconjugates | MONSANTO COMPANY (US) | 1993-05-18 | — | — | US | claimed |
| EP-0413675-A2 | Method for producing synthetic N-linked glycoconjugates | OXFORD GLYCOSYSTEMS LTD. (GB) | 1991-02-20 | — | — | EP | claimed |
| JP-3083993-A | — | — | None | — | — | JP | disclosed |
| US-6251858-B1 | DERIVATIVES OF GLYCOSYLAMINE IN WHICH THE OLIGOSIDES ARE FIXED ON AT LEAST ONE MOLECULE, MATRIX OR PARTICLE | I.D.M. IMMUNO-DESIGNED MOLECULES (FR) | 2001-06-26 | — | — | US | disclosed |
| EP-0766689-B1 | NOVEL OLIGOSACCHARIDE DERIVATIVES, PREPARATION METHOD THEREFOR AND USES THEREOF | IDM IMMUNO DESIGNED MOLECULES (FR) | 1999-10-20 | — | — | EP | disclosed |
| EP-0832898-A2 | Substituted amino acid derivatives | BAYER AG (DE) | 1998-04-01 | — | — | EP | disclosed |
| EP-0766689-A1 | NOVEL OLIGOSACCHARIDE DERIVATIVES, PREPARATION METHOD THEREFOR AND USES THEREOF | I.D.M. IMMUNO-DESIGNED MOLECULES (FR) | 1997-04-09 | — | — | EP | disclosed |
| WO-1996000229-A1 | NOVEL OLIGOSACCHARIDE DERIVATIVES, PREPARATION METHOD THEREFOR AND USES THEREOF | I.D.M. IMMUNO-DESIGNED MOLECULES (FR) | 1996-01-04 | — | — | WO | disclosed |
| EP-0413675-B1 | Method for producing synthetic N-linked glycoconjugates | MONSANTO CO (US) | 1995-05-03 | — | — | EP | disclosed |
| US-5280113-A | Reacting oligosaccharide with ammonium bicarbonate; then a peptide | MONSANTO COMPANY (US) | 1994-01-18 | — | — | US | disclosed |
| US-5212298-A | Method for producing synthetic N-linked glycoconjugates | MONSANTO COMPANY (US) | 1993-05-18 | — | — | US | disclosed |
| EP-0538230-A1 | Method for producing synthetic N-linked glycoconjugates | OXFORD GLYCOSYSTEMS LTD. (GB) | 1993-04-21 | — | — | EP | disclosed |
| JP-H0383993-A | PREPARATION OF SYNTHETIC N-COMBINATION HETEROSACCHARIDE | MONSANTO CO | 1991-04-09 | — | — | JP | disclosed |
| EP-0413675-A2 | Method for producing synthetic N-linked glycoconjugates | OXFORD GLYCOSYSTEMS LTD. (GB) | 1991-02-20 | — | — | EP | disclosed |