Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.42 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.42 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.40 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.37 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.37 |
| ▸ | MAPT | P10636 | 1/20 | 0.34 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.31 |
| ▸ | PDE4A | P27815 | 1/20 | 0.31 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.31 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL374291 | 0.94 | LMNA (0.46) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL1859978 | 0.90 | L3MBTL1 (0.37) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL7157902 | 0.84 | L3MBTL1 (0.41) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL6436844 | 0.82 | LMNA (0.46) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL4650446 | 0.82 | LMNA (0.46) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL17255899 | 0.82 | LMNA (0.46) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL1870865 | 0.77 | GAA (0.32) | LMNAL3MBTL1 | |
| SCHEMBL13955722 | 0.76 | LMNA (0.50) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL15013156 | 0.76 | LMNA (0.43) | LMNAL3MBTL1TDP1CYP2C19HIF1A | |
| SCHEMBL4444063 | 0.75 | SLC6A3 (0.33) | — |
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-1021457-B1 | METHOD FOR THE SITE SPECIFIC SYNTHESIS OF NOVEL 3-HYDROXYPYRIDIN-4(1H)-ONES DERIVATIVES FROM AMINOITOLS, PRODUCTS OBTAINED BY THIS METHOD AND THEIR APPLICATIONS | ISTITUTO BIOCHIMICO PAVESE PHA (IT) | 2003-04-09 | — | — | EP | disclosed |
| US-6177409-B1 | 2-(ALKYL OR HALOALKYL)-3-HYDROXY PYRAN-4-ONE IS HYDROXYL-PROTECTED, AND REACTED WITH AN AMINO ITOL TO SUBSTITUTED THE INTRACYCLIC OXYGEN OF PYRANONE WITH THE AMINE OF THE AMINO ITOL; IRON(III) CHELATORS FOR BLOOD DISORDERS | INSTITUTO BIOCHIMICO PAVESE PHARMA S.P.A. (IT) | 2001-01-23 | — | — | US | disclosed |
| EP-1021457-A1 | METHOD FOR THE SITE SPECIFIC SYNTHESIS OF NOVEL 3-HYDROXYPYRIDIN-4(1H)-ONS DERIVATIVES FROM AMINOMONOSACCHARIDES OR AMINOITOLS, PRODUCTS OBTAINED BY THIS METHOD AND THEIR APPLICATIONS | Istituto Biochimico Pavese Pharma SPA (IT) | 2000-07-26 | — | — | EP | disclosed |
| WO-1998001458-A1 | METHOD FOR THE SITE SPECIFIC SYNTHESIS OF NOVEL 3-HYDROXYPYRIDIN-4(1H)-ONS DERIVATIVES FROM AMINOMONOSACCHARIDES OR AMINOITOLS, PRODUCTS OBTAINED BY THIS METHOD AND THEIR APPLICATIONS | ISTITUTO BIOCHIMICO PAVESE PHARMA SPA (IT) | 1998-01-15 | — | — | WO | disclosed |