Predicted protein targets (top 7)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ESR2 | Q92731 | 18/20 | 0.60 |
| ▸ | DEGS1 | O15121 | 1/20 | 0.56 |
| ▸ | ESR1 | P03372 | 6/20 | 0.55 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.55 |
| ▸ | CYP2C9 | P11712 | 2/20 | 0.55 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.55 |
| ▸ | KDM1A | O60341 | 1/20 | 0.48 |
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 | |
|---|---|---|---|---|
| SCHEMBL19665791 | 0.98 | ESR2 (0.62) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL698289 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL28569320 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL5581754 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL698472 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL28542248 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL2095018 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL699003 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL28538819 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 | |
| SCHEMBL218897 | 0.93 | ESR2 (0.67) | ESR2DEGS1ESR1CYP3A4CYP2C9 |
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 7 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-104379545-B | The manufacture method of 4,4 \"-dihydroxy-meta-terphenyl class | 本州化学工业株式会社 | 2016-08-24 | — | — | CN | disclosed |
| US-20070104894-A1 | POLYMERIZABLE LIQUID CRYSTAL COMPOUND, LIQUID CRYSTAL COMPOSITION, OPTICAL ANISOTROPIC MATERIAL AND OPTICAL ELEMENT | ASAHI GLASS CO., LTD. (JP) | 2007-05-10 | — | — | US | disclosed |
| US-6388146-B1 | AROMATIC UNSATURATED NOMONER | SHARP KABUSHIKI KAISHA (JP) | 2002-05-14 | — | — | US | disclosed |
| US-5175135-A | Using acid mordenite zeolite as alkylation catalysts to produce dialkylbiphenyl | THE DOW CHEMICAL COMPANY (US) | 1992-12-29 | — | — | US | disclosed |
| US-5004841-A | Para-substitutions with crystalline acidic mordenite zeolite alkylation catalysts | THE DOW CHEMICAL COMPANY (US) | 1991-04-02 | — | — | US | disclosed |
| US-4891448-A | ACIDIC MORDENITE CATALYST | THE DOW CHEMICAL COMPANY (US) | 1990-01-02 | — | — | US | disclosed |
| EP-0317907-A2 | Alkylation of polycyclic aromatic compounds to alkylates enriched in the para-substituted isomers | THE DOW CHEMICAL COMPANY (US) | 1989-05-31 | — | — | EP | disclosed |