Predicted protein targets (top 17)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HPGD | P15428 | 1/20 | 0.58 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.58 |
| ▸ | HRH1 | P35367 | 10/20 | 0.55 |
| ▸ | DRD1 | P21728 | 5/20 | 0.55 |
| ▸ | DRD2 | P14416 | 4/20 | 0.55 |
| ▸ | DRD4 | P21917 | 4/20 | 0.55 |
| ▸ | DRD5 | P21918 | 4/20 | 0.55 |
| ▸ | TP53 | P04637 | 1/20 | 0.53 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.53 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.53 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.53 |
| ▸ | TSHR | P16473 | 1/20 | 0.53 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.53 |
| ▸ | DRD3 | P35462 | 4/20 | 0.51 |
| ▸ | LMNA | P02545 | 1/20 | 0.51 |
| ▸ | CALM1 | P0DP23 | 1/20 | 0.50 |
| ▸ | HTR2A | P28223 | 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 | |
|---|---|---|---|---|
| Water SCHEMBL28646770 | 0.98 | HPGD (0.56) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL28180000 | 0.89 | HRH1 (0.58) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL15940347 | 0.87 | HPGD (0.47) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| Phosphine SCHEMBL28179254 | 0.87 | HRH1 (0.56) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| Di(Hydroxyethyl)Ether SCHEMBL7755727 | 0.85 | HPGD (0.50) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL7033288 | 0.85 | HPGD (0.49) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL17644776 | 0.85 | SLC5A1 (0.48) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL17644773 | 0.83 | SLC6A4 (0.53) | HPGDSMN1; SMN2HRH1HTR2A | |
| SCHEMBL9234711 | 0.83 | SLC6A4 (0.50) | HPGDSMN1; SMN2HRH1DRD1DRD2 | |
| SCHEMBL11217522 | 0.83 | KEAP1 (0.62) | HPGDSMN1; SMN2HRH1DRD1DRD2 |
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 1043 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-113443970-B | Synthesis method of 4-alkoxy phenol compound | 新乡医学院 | 2023-04-07 | — | — | CN | 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-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 |
| EP-1118609-A2 | Iminooxi-substituted benzyl phenyl ethers, process and intermediates for their preparation, agents containing them as well as their use in combatting harmful fungi | BASF AKTIENGESELLSCHAFT (DE) | 2001-07-25 | — | — | EP | claimed |
| EP-1062208-A1 | HETARYL-SUBSTITUTED BENZYL PHENYL ETHERS, METHOD FOR THE PRODUCTION THEREOF, AND THEIR USE FOR COMBATING HARMFUL FUNGI AND ANIMAL PESTS | BASF AKTIENGESELLSCHAFT (DE) | 2000-12-27 | — | — | EP | claimed |
| WO-1999046246-A1 | HETARYL-SUBSTITUTED BENZYL PHENYL ETHERS, METHOD FOR THE PRODUCTION THEREOF, AND THEIR USE FOR COMBATING HARMFUL FUNGI AND ANIMAL PESTS | BASF AKTIENGESELLSCHAFT (DE) | 1999-09-16 | — | — | WO | claimed |
| EP-0408995-B1 | Liquid crystal medium with limited temperature-dependence of the d/p coefficient | MERCK PATENT GMBH (DE) | 1995-11-08 | — | — | EP | claimed |
| EP-0437480-B1 | METHOD AND APPARATUS FOR CONTINUOUS CHEMICAL REACTIONS | COMMW SCIENT IND RES ORG (AU) | 1994-10-19 | — | — | EP | claimed |
| EP-0152808-B1 | NITROGEN CONTAINING HETEROCYCLES | MERCK PATENT GmbH (DE) | 1990-09-12 | — | — | EP | claimed |
| EP-0209622-B1 | HYDROTERPHENYLS | MERCK PATENT GmbH (DE) | 1989-06-07 | — | — | EP | claimed |
| EP-0133103-B1 | BENZYL-PHENYL OSIDES, PROCESS FOR THEIR PREPARATION AND THEIR USE | FOURNIER INNOVATION ET SYNERGIE (FR) | 1987-11-11 | — | — | EP | claimed |
| EP-0133103-A1 | Benzyl-phenyl osides, process for their preparation and their use | FOURNIER INNOVATION ET SYNERGIE (FR) | 1985-02-13 | — | — | EP | claimed |
| EP-0044536-A1 | Plant growth regulators and their use | J.T. Baker Chemical Co. (US) | 1982-01-27 | — | — | EP | claimed |