⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL16599779 | 0.79 | — | — | |
| Water SCHEMBL28435262 | 0.76 | TSHR (0.41) | — | |
| SCHEMBL3699750 | 0.72 | — | — | |
| SCHEMBL3689675 | 0.72 | TSHR (0.53) | — | |
| SCHEMBL14932100 | 0.71 | CA4 (0.32) | — | |
| SCHEMBL8645636 | 0.71 | — | — | |
| SCHEMBL61227 | 0.71 | — | — | |
| SCHEMBL1965420 | 0.71 | — | — | |
| SCHEMBL108620 | 0.71 | — | — | |
| SCHEMBL4932934 | 0.69 | — | — |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118480154-A | Synthesis method of quaternary amine acrylic ester active composite monomer grafted xylan/resveratrol lactobionic acid ester | 桂林理工大学 | 2024-08-13 | — | — | CN | claimed |
| CN-118184886-A | Synthesis method of stilbene triphenol and bagasse xylan composite esterified grafted high-fluorine derivative | 桂林理工大学 | 2024-06-14 | — | — | CN | claimed |
| CN-118165185-A | Method for synthesizing composite BX/Res biomass nano active material by using rectorite as catalyst | 桂林理工大学 | 2024-06-11 | — | — | CN | claimed |
| CN-118480154-A | Synthesis method of quaternary amine acrylic ester active composite monomer grafted xylan/resveratrol lactobionic acid ester | 桂林理工大学 | 2024-08-13 | — | — | CN | disclosed |
| CN-118184886-A | Synthesis method of stilbene triphenol and bagasse xylan composite esterified grafted high-fluorine derivative | 桂林理工大学 | 2024-06-14 | — | — | CN | disclosed |
| CN-118165185-A | Method for synthesizing composite BX/Res biomass nano active material by using rectorite as catalyst | 桂林理工大学 | 2024-06-11 | — | — | CN | disclosed |
| US-RE32992-E | THERAPY FOR INFECTIOUS DISEASES CAUSED BY PATHOGENIC MICROORGANISMS | Fujisawa Pharaceutical Co., Ltd. (JP) | 1989-07-18 | — | — | US | disclosed |
| US-4801580-A | Peptide, process for preparation thereof and use thereof | FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) | 1989-01-31 | — | — | US | disclosed |
| US-4749691-A | Peptide, process for preparation thereof and use thereof | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 1988-06-07 | — | — | US | disclosed |
| US-4725582-A | IMMUNE RESPONSE ENHANCERS | FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) | 1988-02-16 | — | — | US | disclosed |
| EP-0025842-B1 | PEPTIDES, PROCESS FOR THEIR PREPARATION, THEIR PHARMACEUTICAL COMPOSITIONS AND THEIR INTERMEDIATES | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 1987-06-03 | — | — | EP | disclosed |
| US-4539155-A | New peptide, process for preparation thereof and use thereof | FUISAWA PHARMACEUTICAL COMPANY, LTD. (JP) | 1985-09-03 | — | — | US | disclosed |
| US-4504584-A | PEPTIDE | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 1985-03-12 | — | — | US | disclosed |
| US-4458078-A | SYNTHESIS OF OLIGOPEPTIDES | FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) | 1984-07-03 | — | — | US | disclosed |
| US-4311640-A | ANTIBIOTIC | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 1982-01-19 | — | — | US | disclosed |
| EP-0025842-A2 | Peptides, process for their preparation, their pharmaceutical compositions and their intermediates | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 1981-04-01 | — | — | EP | disclosed |