Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | AHR | P35869 | 1/20 | 0.61 |
| ▸ | NFE2L2 | Q16236 | 2/20 | 0.59 |
| ▸ | MAOB | P27338 | 3/20 | 0.56 |
| ▸ | CYP19A1 | P11511 | 1/20 | 0.56 |
| ▸ | MAOA | P21397 | 1/20 | 0.56 |
| ▸ | CYP1B1 | Q16678 | 1/20 | 0.55 |
| ▸ | TSHR | P16473 | 1/20 | 0.53 |
| ▸ | RELA | Q04206 | 2/20 | 0.50 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.50 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.50 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.50 |
| ▸ | PPARG | P37231 | 1/20 | 0.50 |
| ▸ | EGFR | P00533 | 1/20 | 0.50 |
| ▸ | MMP1 | P03956 | 1/20 | 0.50 |
| ▸ | MMP2 | P08253 | 1/20 | 0.50 |
| ▸ | MMP9 | P14780 | 1/20 | 0.50 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.48 |
| ▸ | MEN1 | O00255 | 1/20 | 0.48 |
| ▸ | NPC1 | O15118 | 1/20 | 0.48 |
| ▸ | ALDH1A1 | P00352 | 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 | |
|---|---|---|---|---|
| SCHEMBL699518 | 1.00 | AHR (0.61) | AHRNFE2L2MAOBCYP19A1MAOA | |
| SCHEMBL18416526 | 1.00 | AHR (0.61) | AHRNFE2L2MAOBCYP19A1MAOA | |
| SCHEMBL14947044 | 1.00 | AHR (0.61) | AHRNFE2L2MAOBCYP19A1MAOA | |
| SCHEMBL9971887 | 0.93 | CYP1A2 (0.64) | AHRNFE2L2MAOBCYP19A1MAOA | |
| SCHEMBL18416524 | 0.93 | MAOB (0.67) | AHRNFE2L2MAOBCYP19A1MAOA | |
| (Z)-1,2-Diphenylethene SCHEMBL28535457 | 0.92 | TSHR (0.65) | AHRNFE2L2MAOBCYP19A1MAOA | |
| Dimethylamine SCHEMBL5517540 | 0.91 | AHR (0.52) | AHRNFE2L2MAOBCYP19A1MAOA | |
| SCHEMBL2622613 | 0.90 | MAOB (0.70) | AHRNFE2L2MAOBMAOACYP1B1 | |
| SCHEMBL137664 | 0.90 | MAOB (0.70) | AHRNFE2L2MAOBMAOACYP1B1 | |
| SCHEMBL2622601 | 0.90 | MAOB (0.70) | AHRNFE2L2MAOBMAOACYP1B1 |
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 127 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6258504-B1 | Toner containing resin prepared by a combination of emulsion followed by suspension polymerization | NASHUA CORPORATION | 2001-07-10 | — | — | US | claimed |
| EP-1093027-A1 | Toner containing resin prepared by a combination of emulsion followed by suspension polymerization | Nashua Corporation (US) | 2001-04-18 | — | — | EP | claimed |
| CN-118843614-A | High-purity 4- (2-bromoethyl) benzenesulfonic acid, high-purity styrenesulfonic acid derived therefrom, polymer thereof, and process for producing these | 东曹精细化工株式会社 | 2024-10-25 | — | — | CN | disclosed |
| WO-2021074275-A1 | EFFECTIVE PHOTOMODULATION OF LANTHANIDE (III) ION LUMINESCENCE IN THE VISIBLE OR NEAR-INFRARED RANGE | UNIVERSITE DE RENNES 1 (FR) | 2021-04-22 | — | — | WO | disclosed |
| CN-108473415-B | Triphenylamine derivative, charge transport material using the same, and electrophotographic photoreceptor | 高砂香料工业株式会社 | 2021-02-02 | — | — | CN | disclosed |
| CN-108658718-B | Preparation method of trans-stilbene compound | 温州大学 | 2020-12-18 | — | — | CN | disclosed |
| CN-111233610-A | Synthesis method of trans-olefin compound | 五邑大学 | 2020-06-05 | — | — | CN | disclosed |
| CN-110256192-A | It is a kind of using alcohol be hydrogen source Photocatalysis selectivity synthesis cis and trans olefins process | 南通大学 | 2019-09-20 | — | — | CN | disclosed |
| CN-110218141-A | A kind of Photocatalysis selectivity synthesis Z- and E- olefins process | 南通大学 | 2019-09-10 | — | — | CN | disclosed |
| CN-109134172-A | The alcohol hydrogen supply iridium catalytic selectivity of ligand regulation synthesizes Z- and E- olefins process | 南通大学 | 2019-01-04 | — | — | CN | disclosed |
| CN-105837410-B | A kind of preparation method replacing cis-form olefin | 大连理工大学 | 2018-12-21 | — | — | CN | disclosed |
| US-5633109-A | Ink compositions with liposomes containing photochromic compounds | XEROX CORPORATION (US) | 1997-05-27 | — | — | US | disclosed |
| US-5593486-A | Photochromic hot melt ink compositions | XEROX CORPORATION (US) | 1997-01-14 | — | — | US | disclosed |
| US-5551973-A | LIQUID CRYSTAL GEL PHASE, MICROEMULSION PHASE | XEROX CORPORATION (US) | 1996-09-03 | — | — | US | disclosed |
| EP-0157420-A2 | Amide derivatives and 5-lipoxygenase inhibitors containing the same as an active ingredient | TERUMO KABUSHIKI KAISHA trading as TERUMO CORPORATION (JP) | 1985-10-09 | — | — | EP | disclosed |
| US-4420435-A | Alpha-hydroxy-phosphonic acid esters | BAYER AKTIENGESELLSCHAFT (DE) | 1983-12-13 | — | — | US | disclosed |
| EP-0041043-B1 | PROCESS FOR THE PREPARATION OF DERIVATIVES OF ALKENYL BENZENE OR ALKENYL NAPHTHALENE | CIBA-GEIGY AG (CH) | 1983-11-09 | — | — | EP | disclosed |
| US-4358409-A | Preparation of styryl cyclopropane insecticide intermediates | BAYER AKTIENGESELLSCHAFT (DE) | 1982-11-09 | — | — | US | disclosed |
| US-4335055-A | Process for the preparation of alkenylbenzene derivatives or alkenylnaphthalene derivatives | CIBA-GEIGY CORPORATION (US) | 1982-06-15 | — | — | US | disclosed |
| EP-0041043-A1 | Process for the preparation of derivatives of alkenyl benzene or alkenyl naphthalene | CIBA-GEIGY AG (CH) | 1981-12-02 | — | — | EP | disclosed |