Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TAAR1 | Q96RJ0 | 3/20 | 0.62 |
| ▸ | IDO1 | P14902 | 2/20 | 0.62 |
| ▸ | AGXT | P21549 | 2/20 | 0.62 |
| ▸ | CHRM2 | P08172 | 3/20 | 0.58 |
| ▸ | CHRM1 | P11229 | 2/20 | 0.58 |
| ▸ | CHRM3 | P20309 | 2/20 | 0.58 |
| ▸ | CMA1 | P23946 | 1/20 | 0.56 |
| ▸ | MAOB | P27338 | 2/20 | 0.55 |
| ▸ | SIGMAR1 | Q99720 | 2/20 | 0.55 |
| ▸ | AOC3 | Q16853 | 1/20 | 0.55 |
| ▸ | LPO | P22079 | 1/20 | 0.53 |
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 | |
|---|---|---|---|---|
| SCHEMBL29908907 | 1.00 | TAAR1 (0.62) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| Bromide SCHEMBL28187051 | 0.98 | TAAR1 (0.60) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| Ammonia Solution, Strong SCHEMBL265549 | 0.98 | TAAR1 (0.60) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| Fluoride SCHEMBL27638425 | 0.98 | TAAR1 (0.60) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| Methyl Alcohol SCHEMBL11157985 | 0.94 | IDO1 (0.59) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| SCHEMBL10796146 | 0.89 | MAPK1 (0.60) | TAAR1IDO1AGXTMAOB | |
| SCHEMBL13462942 | 0.89 | MAOB (0.69) | IDO1AGXTMAOB | |
| SCHEMBL18015799 | 0.88 | MAOB (0.56) | TAAR1IDO1AGXTMAOBSIGMAR1 | |
| SCHEMBL11221585 | 0.87 | TAAR1 (0.54) | TAAR1IDO1AGXTCHRM2CHRM1 | |
| Phenol SCHEMBL28160826 | 0.87 | MAOB (0.57) | TAAR1IDO1AGXTMAOBSIGMAR1 |
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
Appears in 3089 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20260002924-A1 | METHOD FOR SELECTING ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS FROM MIXTURE OF ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS AND OTHER TYPES OF POLYMERS | KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) | 2026-01-01 | — | — | US | claimed |
| CN-120040272-A | Method for producing m-ethyl anisole and p-ethyl anisole by using xylenol oil | 煤炭科学技术研究院有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-117820088-B | Preparation method of m-ethylanisole | 万华化学集团股份有限公司 | 2025-02-18 | — | — | CN | claimed |
| CN-119384454-A | Depolymerization process of polymers containing ester functionalities using mixed organic solvents | 韩国化学研究院 | 2025-01-28 | — | — | CN | claimed |
| EP-4477693-A1 | METHOD FOR SELECTING ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS FROM MIXTURE OF ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS AND OTHER TYPES OF POLYMERS | Korea Research Institute of Chemical Technology (KR) | 2024-12-18 | — | — | EP | claimed |
| CN-118026860-A | Preparation method of 3- [1- (dimethylamino) ethyl ] phenol | 福建福瑞明德药业有限公司 | 2024-05-14 | — | — | CN | claimed |
| CN-117820088-A | Preparation method of m-ethylanisole | 万华化学集团股份有限公司 | 2024-04-05 | — | — | CN | claimed |
| WO-2024005445-A1 | METHOD FOR DEPOLYMERIZATION OF POLYMER CONTAINING ESTER FUNCTIONAL GROUP BY USING MIXTURE ORGANIC SOLVENT | 한국화학연구원 | 2024-01-04 | — | — | WO | claimed |
| WO-2023195794-A1 | METHOD FOR SELECTING ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS FROM MIXTURE OF ESTER FUNCTIONAL GROUP-CONTAINING POLYMERS AND OTHER TYPES OF POLYMERS | 한국화학연구원 | 2023-10-12 | — | — | WO | claimed |
| CN-106518750-B | Carbazole amino alcohol compound, preparation method thereof and application of carbazole amino alcohol compound in resisting parasitic diseases | 中国疾病预防控制中心寄生虫病预防控制所 | 2021-06-01 | — | — | CN | claimed |
| WO-1998019693-A1 | COMBINATORIAL LIBRARIES OF CYCLIC UREA AND CYCLIC THIOUREA DERIVATIVES AND COMPOUNDS THEREIN | TREGA BIOSCIENCES, INC. (US) | 1998-05-14 | — | — | WO | claimed |
| EP-0822814-A1 | ALPHA 1a ADRENERGIC RECEPTOR ANTAGONISTS | Merck & Co., Inc. (US) | 1998-02-11 | — | — | EP | claimed |
| WO-1996032938-A1 | ALPHA 1a ADRENERGIC RECEPTOR ANTAGONISTS | MERCK & CO., INC. (US) | 1996-10-24 | — | — | WO | claimed |
| EP-0264908-B1 | High sensitivity resists having autodecomposition temperatures greater than about 160 C | IBM (US) | 1996-03-20 | — | — | EP | claimed |
| EP-0370054-B1 | CATALYST COMPOSITION AND METHOD FOR SELECTIVE DEHYDROGENATION | EASTMAN KODAK COMPANY (a New Jersey corporation) (US) | 1992-01-15 | — | — | EP | claimed |
| US-4931379-A | ADDITION POLYMERS HAVING PENDANT ACID-LABILE GROUPS, E.G CARBONATES, AND SIDECHAINS FOR ADDED STABILITY; SEMICONDUCTORS; MICROLITHOGRAPHY | INTERNATIONAL BUSINESS MACHINES CORPORATION (US) | 1990-06-05 | — | — | US | claimed |
| EP-0264908-A2 | High sensitivity resists having autodecomposition temperatures greater than about 160 C | International Business Machines Corporation (US) | 1988-04-27 | — | — | EP | claimed |
| EP-0251194-A1 | Use of carbocyclic and heterocyclic condensed dihydropyridines for the preparation of cardioprotective remedies and heterocyclic and carbocyclic condensed dihydropyridines and methods and intermediates for their preparation | BOEHRINGER INGELHEIM KG (DE) | 1988-01-07 | — | — | EP | claimed |
| US-4473713-A | Hydrolysis of aryl-aliphatic ethers | RHONE-POULENC SPECIALITES CHIMIQUES (FR) | 1984-09-25 | — | — | US | claimed |
| US-4102929-A | Asymmetric synthesis of organic compounds | HOFFMANN-LA ROCHE INC. (US) | 1978-07-25 | — | — | US | claimed |