Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | OPRL1 | P41146 | 2/20 | 0.40 |
| ▸ | NUDT1 | P36639 | 1/20 | 0.39 |
| ▸ | BACE1 | P56817 | 1/20 | 0.39 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.39 |
| ▸ | HSP90AB1 | P08238 | 1/20 | 0.39 |
| ▸ | PSMB5 | P28074 | 1/20 | 0.38 |
| ▸ | ESR1 | P03372 | 1/20 | 0.38 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.38 |
| ▸ | CHRNB2 | P17787 | 1/20 | 0.38 |
| ▸ | CHRNA4 | P43681 | 1/20 | 0.38 |
| ▸ | PTGDR2 | Q9Y5Y4 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL14115860 | 0.98 | HSP90AB1 (0.40) | OPRL1HSP90AB1ESR1ESR2CHRNB2 | |
| SCHEMBL16232086 | 0.94 | ESR2 (0.39) | ESR1ESR2CHRNB2CHRNA4 | |
| SCHEMBL16553931 | 0.90 | CHRNB2 (0.41) | OPRL1ESR1ESR2CHRNB2CHRNA4 | |
| SCHEMBL9785240 | 0.85 | PTGDR2 (0.41) | NUDT1BACE1HSP90AA1HSP90AB1PSMB5 | |
| SCHEMBL17699117 | 0.82 | CHRNB2 (0.55) | NUDT1BACE1HSP90AA1HSP90AB1ESR1 | |
| SCHEMBL2719727 | 0.81 | ESR2 (0.56) | ESR1ESR2 | |
| SCHEMBL19347098 | 0.81 | HTR2C (0.58) | CHRNB2CHRNA4 | |
| SCHEMBL31131399 | 0.81 | HTR2C (0.58) | CHRNB2CHRNA4 | |
| SCHEMBL27628654 | 0.81 | CHRNB2 (0.37) | ESR1ESR2CHRNB2CHRNA4 | |
| Hydrochloric Acid SCHEMBL25328473 | 0.80 | HTR2C (0.59) | CHRNB2CHRNA4 |
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 37 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8969272-B2 | Hydroxyaromatic functionalized polyalpha-olefins | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2015-03-03 | — | — | US | claimed |
| WO-2014001056-A1 | ANTIMICROBIAL COMPOSITION | UNILEVER N.V. (NL) | 2014-01-03 | — | — | WO | claimed |
| CN-112601668-B | Thermosensitive recording material and color-developing agent | 索理思科技开曼公司 | 2022-07-29 | — | — | CN | disclosed |
| CN-112601668-A | Thermosensitive recording material and color-developing agent | 索理思科技开曼公司 | 2021-04-02 | — | — | CN | disclosed |
| EP-2137193-B1 | SUBSTITUTED DIHYDRO AND TETRAHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF | SANOFI SA (FR) | 2017-08-09 | — | — | EP | disclosed |
| US-8999631-B2 | Primer and pattern forming method for layer including block copolymer | TOKYO OHKA KOGYO CO., LTD. (JP) | 2015-04-07 | — | — | US | disclosed |
| CN-104447792-A | Substituted dihydro and tetrahydro oxazolopyrimidinones, preparation and use thereof | SANOFI AVENTIS | 2015-03-25 | — | — | CN | disclosed |
| US-8969272-B2 | Hydroxyaromatic functionalized polyalpha-olefins | EXXONMOBIL CHEMICAL PATENTS INC. (US) | 2015-03-03 | — | — | US | disclosed |
| US-8956810-B2 | — | — | 2015-02-17 | — | — | US | disclosed |
| US-8642603-B2 | Substituted dihydro and tetrahydro oxazolopyrimidinones, preparation and use thereof | SANOFI (FR) | 2014-02-04 | — | — | US | disclosed |
| US-20140030652-A1 | PRIMER AND PATTERN FORMING METHOD FOR LAYER INCLUDING BLOCK COPOLYMER | RIKEN (JP) | 2014-01-30 | — | — | US | disclosed |
| CN-1031188-C | Process for producing hydroxy group-containing alkyl aromatic compound | SUMITOMO CHEMICAL CO (JP) | 1996-03-06 | — | — | CN | disclosed |
| EP-0249415-B2 | Production of alkylated hydroxy aromatic compounds | SUMITOMO CHEMICAL CO (JP) | 1995-11-15 | — | — | EP | disclosed |
| WO-1994028035-A1 | POLYMER ALKYLATION OF HYDROXYAROMATIC COMPOUNDS | EXXON CHEMICAL PATENTS INC. (US) | 1994-12-08 | — | — | WO | disclosed |
| US-5334775-A | Reacting with a terminally unsaturated polymer in the presence of a partially or completely dehydrated heteropoly catalyst; precursors for production of fuel and lubricant additives | EXXON CHEMICAL PATENTS INC. (US) | 1994-08-02 | — | — | US | disclosed |
| US-RE34076-E | Alkylation catalysis of aromatic alcohol with alkylating agent in presence of heteropoly acid and water | SUMITOMO CHEMICAL COMPANY LIMITED (JP) | 1992-09-22 | — | — | US | disclosed |
| US-4912264-A | Liquid phase alkylation of a hydroxyl containing aromatic compound | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-03-27 | — | — | US | disclosed |
| CN-87104109-A | Process for producing hydroxy group-containing alkyl aromatic compound | — | 1988-01-20 | — | — | CN | disclosed |
| EP-0249415-A2 | Production of alkylated hydroxy aromatic compounds | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1987-12-16 | — | — | EP | disclosed |
| US-3992455-A | CHEMICAL INTERMEDIATES FOR INSECTICIDES | KOPPERS COMPANY, INC. (US) | 1976-11-16 | — | — | US | disclosed |