Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LPAR3 | Q9UBY5 | 7/20 | 0.41 |
| ▸ | LPAR2 | Q9HBW0 | 5/20 | 0.41 |
| ▸ | LPAR1 | Q92633 | 4/20 | 0.41 |
| ▸ | FDPS | P14324 | 2/20 | 0.41 |
| ▸ | TPI1 | P60174 | 1/20 | 0.38 |
| ▸ | SMPD1 | P17405 | 1/20 | 0.36 |
| ▸ | S1PR1 | P21453 | 4/20 | 0.36 |
| ▸ | S1PR3 | Q99500 | 4/20 | 0.36 |
| ▸ | FBP1 | P09467 | 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 | |
|---|---|---|---|---|
| SCHEMBL6413988 | 0.77 | LPAR3 (0.43) | LPAR3LPAR2LPAR1TPI1S1PR1 | |
| SCHEMBL29011380 | 0.76 | LPAR3 (0.43) | LPAR3LPAR2LPAR1FDPSSMPD1 | |
| Ethylamine SCHEMBL28263292 | 0.76 | LPAR3 (0.39) | LPAR3LPAR2LPAR1FDPSTPI1 | |
| SCHEMBL8060222 | 0.76 | FBP1 (0.39) | LPAR3LPAR2LPAR1FDPSTPI1 | |
| Ammonia Solution, Strong SCHEMBL26660491 | 0.75 | LMNA (0.38) | LPAR3LPAR2LPAR1TPI1SMPD1 | |
| SCHEMBL14582611 | 0.75 | LPAR3 (0.41) | LPAR3LPAR2LPAR1TPI1S1PR1 | |
| SCHEMBL7158770 | 0.75 | LPAR3 (0.41) | LPAR3LPAR2LPAR1SMPD1S1PR1 | |
| SCHEMBL7157667 | 0.75 | LPAR3 (0.42) | LPAR3LPAR2LPAR1FDPSSMPD1 | |
| SCHEMBL993812 | 0.74 | FDPS (0.44) | LPAR3LPAR2FDPS | |
| SCHEMBL5974079 | 0.74 | LPAR3 (0.39) | LPAR3LPAR2LPAR1FDPSTPI1 |
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 8 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-5563266-A | Method of use of disubstituted monochlorotriazines | GENERAL ELECTRIC COMPANY (US) | 1996-10-08 | — | — | US | claimed |
| US-5446155-A | Reacting monoorganoxy dichloro-triazine with monohydroxy aliphatic compound in non-polar solvent and aqueous alkali metal hydroxide solution with the presence of phase transfer catalysts | GENERAL ELECTRIC COMPANY (US) | 1995-08-29 | — | — | US | claimed |
| EP-0592143-A1 | Method for preparing disubstituted monochlorotriazines | GENERAL ELECTRIC COMPANY (US) | 1994-04-13 | — | — | EP | claimed |
| CN-115995606-B | Non-aqueous electrolyte of lithium ion battery and lithium ion battery | 诺莱特电池材料(苏州)有限公司 | 2024-10-15 | — | — | CN | disclosed |
| CN-115995606-A | Non-aqueous electrolyte of lithium ion battery and lithium ion battery | 诺莱特电池材料(苏州)有限公司 | 2023-04-21 | — | — | CN | disclosed |
| US-5563266-A | Method of use of disubstituted monochlorotriazines | GENERAL ELECTRIC COMPANY (US) | 1996-10-08 | — | — | US | disclosed |
| US-5446155-A | Reacting monoorganoxy dichloro-triazine with monohydroxy aliphatic compound in non-polar solvent and aqueous alkali metal hydroxide solution with the presence of phase transfer catalysts | GENERAL ELECTRIC COMPANY (US) | 1995-08-29 | — | — | US | disclosed |
| EP-0592143-A1 | Method for preparing disubstituted monochlorotriazines | GENERAL ELECTRIC COMPANY (US) | 1994-04-13 | — | — | EP | disclosed |