Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NAAA | Q02083 | 2/20 | 0.40 |
| ▸ | CTSK | P43235 | 1/20 | 0.40 |
| ▸ | FFAR4 | Q5NUL3 | 1/20 | 0.38 |
| ▸ | CYP17A1 | P05093 | 1/20 | 0.37 |
| ▸ | HCRTR1 | O43613 | 6/20 | 0.37 |
| ▸ | HCRTR2 | O43614 | 6/20 | 0.37 |
| ▸ | S1PR1 | P21453 | 1/20 | 0.36 |
| ▸ | EPHX2 | P34913 | 3/20 | 0.36 |
| ▸ | RARB | P10826 | 2/20 | 0.36 |
| ▸ | RARA | P10276 | 1/20 | 0.36 |
| ▸ | RARG | P13631 | 1/20 | 0.36 |
| ▸ | GPR84 | Q9NQS5 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL8748046 | 0.93 | RARB (0.39) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8747985 | 0.92 | RARB (0.41) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8747918 | 0.91 | RARB (0.43) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8748030 | 0.91 | RARB (0.43) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8018485 | 0.90 | HCRTR1 (0.41) | HCRTR1HCRTR2EPHX2 | |
| SCHEMBL8031029 | 0.89 | HCRTR1 (0.41) | HCRTR1HCRTR2EPHX2 | |
| SCHEMBL7770288 | 0.87 | NAAA (0.36) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8034592 | 0.87 | EPHX2 (0.38) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL7770286 | 0.87 | NAAA (0.36) | NAAACTSKFFAR4CYP17A1HCRTR1 | |
| SCHEMBL8834365 | 0.87 | CYP17A1 (0.33) | NAAACTSKFFAR4CYP17A1S1PR1 |
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 2 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6013198-A | LIQUID CRYSTALLINE COMPOUNDS MODIFIED TO HAVE A TRIFLUOROMETHYLPHENYL GROUP OR TRIFLUOROMETHOXYPHENYL GROUP AS EXAMPLE OF KNOWN TERMINAL SUBSTITUENT; CHEMICAL STABILITY, HIGH VOLTAGE HOLDING RATIO, GOOD UV STABILITY | CHISSO CORPORATION (JP) | 2000-01-11 | — | — | US | disclosed |
| EP-0761799-A1 | Liquid crystalline compound substituted with fluorine containing group, liquid crystal composition, and liquid crystal display device | Chisso Corporation (JP) | 1997-03-12 | — | — | EP | disclosed |