Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LTA4H | P09960 | 7/20 | 0.67 |
| ▸ | SRD5A2 | P31213 | 1/20 | 0.64 |
| ▸ | CALM1 | P0DP23 | 1/20 | 0.63 |
| ▸ | TSHR | P16473 | 1/20 | 0.55 |
| ▸ | IDH1 | O75874 | 1/20 | 0.52 |
| ▸ | FFAR1 | O14842 | 1/20 | 0.50 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.50 |
| ▸ | ACACB | O00763 | 1/20 | 0.49 |
| ▸ | ACACA | Q13085 | 1/20 | 0.49 |
| ▸ | GRIN1 | Q05586 | 1/20 | 0.49 |
| ▸ | GRIN2B | Q13224 | 1/20 | 0.49 |
| ▸ | PPARG | P37231 | 3/20 | 0.48 |
| ▸ | PPARA | Q07869 | 3/20 | 0.48 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.48 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.48 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.48 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.48 |
| ▸ | HTT | P42858 | 1/20 | 0.48 |
| ▸ | HRH1 | P35367 | 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 | |
|---|---|---|---|---|
| SCHEMBL7178244 | 1.00 | LTA4H (0.67) | LTA4HSRD5A2CALM1TSHRIDH1 | |
| SCHEMBL10269397 | 0.97 | SRD5A2 (0.68) | LTA4HSRD5A2CALM1TSHRIDH1 | |
| SCHEMBL23098203 | 0.95 | SRD5A2 (0.70) | LTA4HSRD5A2CALM1TSHRFFAR1 | |
| SCHEMBL9906839 | 0.95 | SRD5A2 (0.70) | LTA4HSRD5A2CALM1TSHRFFAR1 | |
| SCHEMBL5943308 | 0.89 | LTA4H (0.55) | LTA4HSRD5A2CALM1TSHRIDH1 | |
| SCHEMBL8732491 | 0.89 | MAOA (0.68) | LTA4HSRD5A2CALM1TSHRL3MBTL1 | |
| SCHEMBL20240287 | 0.89 | ST14 (0.63) | LTA4HSRD5A2CALM1 | |
| SCHEMBL15940348 | 0.88 | SRD5A2 (0.58) | LTA4HSRD5A2CALM1TSHRFFAR1 | |
| SCHEMBL9816693 | 0.87 | SRD5A2 (0.58) | LTA4HSRD5A2CALM1TSHRIDH1 | |
| SCHEMBL10053900 | 0.86 | SRD5A2 (0.61) | LTA4HSRD5A2CALM1TSHRFFAR1 |
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 389 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3276696-B1 | FUNCTIONAL LAYER FORMING COMPOSITION AND METHOD FOR MANUFACTURING THE SAME | SEIKO EPSON CORP (JP) | 2023-10-11 | — | — | EP | claimed |
| EP-3315567-B1 | DISPERSANT, DISPERSION, INK COMPOSITION, AND METHODS OF PREPARATION THEREOF | Nissin chemical ind co ltd (JP) | 2023-04-19 | — | — | EP | claimed |
| CN-115920962-A | Simple synthesis of novel triple-effect polyion liquid for efficiently producing lignite-derived aromatic hydrocarbons | 曲阜师范大学 | 2023-04-07 | — | — | CN | claimed |
| CN-113443970-B | Synthesis method of 4-alkoxy phenol compound | 新乡医学院 | 2023-04-07 | — | — | CN | claimed |
| CN-111135844-B | Application of organic soluble molybdenum salt in preparation of molybdenum carbide catalyst, preparation method and application of molybdenum carbide catalyst | 浙江师范大学 | 2023-01-31 | — | — | CN | claimed |
| CN-113083351-B | Application of high-activity ruthenium molecular sieve catalyst Ru/Ga-SH5 in aspect of catalytic hydrodeoxygenation | 中国矿业大学 | 2022-01-14 | — | — | CN | claimed |
| CN-113454187-A | Biologically available chiral dopants for liquid crystal applications | 齐默尔根公司 | 2021-09-28 | — | — | CN | claimed |
| CN-113443970-A | Synthesis method of 4-alkoxy phenol compound | 新乡医学院 | 2021-09-28 | — | — | CN | claimed |
| CN-113083351-A | Application of high-activity ruthenium molecular sieve catalyst Ru/Ga-SH5 in aspect of catalytic hydrodeoxygenation | 中国矿业大学 | 2021-07-09 | — | — | CN | claimed |
| CN-111662270-A | Iodine isotope labeled benzyl phenyl ether derivative, preparation method, pharmaceutical composition and application thereof | 中国医学科学院药物研究所 | 2020-09-15 | — | — | CN | claimed |
| CN-111135844-A | Application of organic soluble molybdenum salt in preparation of molybdenum carbide catalyst, preparation method and application of molybdenum carbide catalyst | 浙江师范大学 | 2020-05-12 | — | — | CN | claimed |
| US-10079342-B2 | Functional layer forming composition, method for producing functional layer forming composition, method for producing organic EL element, organic EL device, and electronic apparatus | SEIKO EPSON CORPORATION (JP) | 2018-09-18 | — | — | US | claimed |
| US-20180062078-A1 | FUNCTIONAL LAYER FORMING COMPOSITION, METHOD FOR PRODUCING FUNCTIONAL LAYER FORMING COMPOSITION, METHOD FOR PRODUCING ORGANIC EL ELEMENT, ORGANIC EL DEVICE, AND ELECTRONIC APPARATUS | SEIKO EPSON CORPORATION (JP) | 2018-03-01 | — | — | US | claimed |
| EP-3276696-A1 | FUNCTIONAL LAYER FORMING COMPOSITION, METHOD FOR MANUFACTURING FUNCTIONAL LAYER FORMING COMPOSITION, METHOD FOR MANUFACTURING ORGANIC EL ELEMENT, ORGANIC EL DEVICE, AND ELECTRONIC EQUIPMENT | Seiko Epson Corporation (JP) | 2018-01-31 | — | — | EP | claimed |
| JP-2053748-A | — | — | None | — | — | JP | disclosed |
| JP-57149241-A | — | — | None | — | — | JP | disclosed |
| WO-2026101568-A1 | MODIFIED REPEAT UNIT FOR ENHANCED INTERACTION ENERGY AND THERMAL STABILITY OF HIGH TEMPERATURE LUBRICANTS FOR MAGNETIC MEDIA | WESTERN DIGITAL TECHNOLOGIES, INC. (US) | 2026-05-15 | — | — | WO | disclosed |
| US-4060593-A | Preparation of titanium trichloride | MITSUBISHI CHEMICAL INDUSTRIES (JA) | 1977-11-29 | — | — | US | disclosed |
| US-4042603-A | SUBSTITUTED DIBENZOFURAN OR 9-FLUORENONE FROM A DIPHENYL ETHER OR BENZOPHENONE | UBE INDUSTRIES, LTD. (JA) | 1977-08-16 | — | — | US | disclosed |
| US-4009185-A | Conversion of diphenylethers to dibenzofurans using catalysts containing ceria | MONSANTO COMPANY (US) | 1977-02-22 | — | — | US | disclosed |