Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GABBR2 | O75899 | 2/20 | 0.56 |
| ▸ | GABBR1 | Q9UBS5 | 2/20 | 0.56 |
| ▸ | GABRR1 | P24046 | 1/20 | 0.56 |
| ▸ | TRPM8 | Q7Z2W7 | 8/20 | 0.46 |
| ▸ | LPAR3 | Q9UBY5 | 3/20 | 0.43 |
| ▸ | LPAR2 | Q9HBW0 | 1/20 | 0.43 |
| ▸ | HPGD | P15428 | 1/20 | 0.42 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.42 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL575350 | 0.94 | GABBR2 (0.52) | GABBR2GABBR1GABRR1TRPM8LPAR3 | |
| SCHEMBL14966563 | 0.90 | LPAR3 (0.55) | GABBR2GABBR1GABRR1TRPM8LPAR3 | |
| SCHEMBL1726446 | 0.88 | LPAR3 (0.59) | TRPM8LPAR3LPAR2 | |
| SCHEMBL575436 | 0.88 | — | — | |
| SCHEMBL8327729 | 0.88 | LPAR3 (0.59) | TRPM8LPAR3LPAR2 | |
| SCHEMBL8330758 | 0.88 | LPAR3 (0.59) | TRPM8LPAR3LPAR2 | |
| SCHEMBL497185 | 0.84 | GABBR2 (0.76) | GABBR2GABBR1GABRR1TRPM8LPAR3 | |
| SCHEMBL10776581 | 0.83 | LPAR3 (0.54) | TRPM8LPAR3LPAR2 | |
| SCHEMBL10786885 | 0.83 | — | — | |
| SCHEMBL152127 | 0.83 | HPGD (0.56) | GABBR2GABBR1GABRR1TRPM8LPAR3 |
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 96 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119303636-A | Catalyst system for ethylene carbonylation reaction | 西南化工研究设计院有限公司 | 2025-01-14 | — | — | CN | claimed |
| EP-2403642-B1 | METHODS OF USING A SELECTIVE HYDROGENATION CATALYST | CHEVRON PHILLIPS CHEMICAL CO LP (US) | 2017-08-02 | — | — | EP | claimed |
| CN-119303636-A | Catalyst system for ethylene carbonylation reaction | 西南化工研究设计院有限公司 | 2025-01-14 | — | — | CN | disclosed |
| US-12100809-B2 | Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery | MITSUBISHI CHEMICAL CORPORATION (JP) | 2024-09-24 | — | — | US | disclosed |
| US-20240297344-A1 | NONAQUEOUS ELECTROLYTE FOR SECONDARY BATTERY AND NONAQUEOUS-ELECTROLYTE SECONDARY BATTERY EMPLOYING THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2024-09-05 | — | — | US | disclosed |
| US-11616253-B2 | Nonaqueous electrolyte for secondary battery and nonaqueous-electrolyte secondary battery employing the same | MITSUBISHI CHEMICAL CORPORATION (JP) | 2023-03-28 | — | — | US | disclosed |
| US-20220278370-A1 | NONAQUEOUS ELECTROLYTE FOR SECONDARY BATTERY AND NONAQUEOUS-ELECTROLYTE SECONDARY BATTERY EMPLOYING THE SAME | MITSUBISHI CHEMICAL CORPORATION (JP) | 2022-09-01 | — | — | US | disclosed |
| US-11367899-B2 | Nonaqueous electrolyte for secondary battery and nonaqueous-electrolyte secondary battery employing the same | MITSUBISHI CHEMICAL CORPORATION (JP) | 2022-06-21 | — | — | US | disclosed |
| US-20220149436-A1 | NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY | MITSUBISHI CHEMICAL CORPORATION (JP) | 2022-05-12 | — | — | US | disclosed |
| US-11283107-B2 | Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery | MITSUBISHI CHEMICAL CORPORATION (JP) | 2022-03-22 | — | — | US | disclosed |
| EP-3144064-B1 | SELECTIVE HYDROGENATION CATALYST AND METHODS OF MAKING AND USING SAME | CHEVRON PHILLIPS CHEMICAL CO LP (US) | 2021-07-28 | — | — | EP | disclosed |
| US-20090325065-A1 | NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY | MITSUBISHI CHEMICAL CORPORATION (JP) | 2009-12-31 | — | — | US | disclosed |
| US-6897343-B2 | Process for the preparation of propanediol | SHELL OIL COMPANY (US) | 2005-05-24 | — | — | US | disclosed |
| US-20040152927-A1 | Process for the preparation of propanediol | SHELL OIL COMPANY | 2004-08-05 | — | — | US | disclosed |
| US-5892121-A | Purification of tertiary phosphine oxides | BASF AKTIENGESELLSCHAFT (DE) | 1999-04-06 | — | — | US | disclosed |
| US-5689005-A | Reductive deoxygenation using a redox catalyst | BASF AKTIENGESELLSCHAFT (DE) | 1997-11-18 | — | — | US | disclosed |
| US-5134236-A | Analgesics, antidepressants, anticonvulsants | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1992-07-28 | — | — | US | disclosed |
| US-4999356-A | Analgesics, antidepressants, anticonvulsants | HOECHST-ROUSSEL PHARMACEUTICALS, INC. (US) | 1991-03-12 | — | — | US | disclosed |
| EP-0302423-A2 | 1-Phenyl-3-(1-piperazinyl)-1h-indazoles, a process and intermediates for their preparation, and the use thereof as medicaments | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1989-02-08 | — | — | EP | disclosed |
| US-4190729-A | Carbonylation process with stabilized catalyst | MONSANTO COMPANY (US) | 1980-02-26 | — | — | US | disclosed |