Known targets — ChEMBL curated mechanism
MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Ethylene Glycol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Ethylene Glycol SCHEMBL8590134 | 1.00 | TSHR (0.75) | — | |
| Ethylene Glycol SCHEMBL27521333 | 1.00 | TSHR (0.75) | — | |
| Ethylene Glycol SCHEMBL10336621 | 1.00 | TSHR (0.75) | — | |
| Ethylene Glycol SCHEMBL27859764 | 0.94 | — | — | |
| Ethylene Glycol SCHEMBL9299266 | 0.94 | — | — | |
| Ethylene Glycol SCHEMBL28255920 | 0.94 | — | — | |
| Ethylene Glycol SCHEMBL15477224 | 0.94 | TSHR (0.67) | — | |
| Ethylene Glycol SCHEMBL9756659 | 0.94 | TSHR (0.67) | — | |
| Ethylene Glycol SCHEMBL8328945 | 0.89 | ALDH1A1 (0.60) | — | |
| Ethylene Glycol SCHEMBL3261295 | 0.89 | — | — |
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 990 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118287111-A | Bismuth molybdate/zinc selenide heterojunction photocatalyst rich in bismuth/molybdenum/zinc vacancies and preparation method and application thereof | 青岛科技大学 | 2024-07-05 | — | — | CN | claimed |
| WO-2024125740-A1 | A METHOD OF EXTRACTING THERMOSET RESIN FRACTIONS FOR DECOMPOSITION AND REUSE | TEKNOLOGISK INSTITUT (DK) | 2024-06-20 | — | — | WO | claimed |
| US-20240173235-A1 | PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS | MOMENTIVE PERFORMANCE MATERIALS INC. | 2024-05-30 | — | — | US | claimed |
| WO-2024108096-A1 | COLD WEATHER OXYGEN ACTIVATED HEATER | RBCE TECH, LLC (US) | 2024-05-23 | — | — | WO | claimed |
| WO-2024086307-A1 | FORMULATED FOOD PRODUCTS | VITAKEY INC. (US) | 2024-04-25 | — | — | WO | claimed |
| WO-2024086306-A1 | FORMULATED FOOD PRODUCTS | VITAKEY INC. (US) | 2024-04-25 | — | — | WO | claimed |
| WO-2024086311-A1 | FORMULATED TASTANT COMPOSITIONS | VITAKEY INC. (US) | 2024-04-25 | — | — | WO | claimed |
| EP-4322915-A1 | PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS | Momentive Performance Materials Inc. (US) | 2024-02-21 | — | — | EP | claimed |
| CN-117551106-A | Preparation method of 6-methylpyrazolopyrimidinone | 金仓(上海)医药生物科技有限公司 | 2024-02-13 | — | — | CN | claimed |
| CN-117229749-A | Method for preparing cross-linked polyurethane hot melt adhesive by taking waste PET as raw material without solvent | 福建省百川资源再生科技股份有限公司 | 2023-12-15 | — | — | CN | claimed |
| EP-0561060-B1 | Composition containing a polymer of unsaturated hydrocarbons, a starch derivative and an ethylene butylacrylate copolymer | CARGILL BV (NL) | 1998-04-29 | — | — | EP | claimed |
| US-5527797-A | IONTOPHORESIS | MACROCHEM CORPORATION (US) | 1996-06-18 | — | — | US | claimed |
| EP-0526026-B1 | Aqueous compositions for use as a printing ink | TIOXIDE SPECIALTIES LTD (GB) | 1995-12-13 | — | — | EP | claimed |
| US-5290825-A | Metal activators and organic acids with metal halides | LCB INTERNATIONAL, INC. | 1994-03-01 | — | — | US | claimed |
| EP-0561060-A1 | Composition containing a polymer of unsaturated hydrocarbon, a C1-4 alkyl- or hydroxyalkylether of starch, an ethylene-butylacrylate copolymer as a compatibilizing agent and a polyhydric aliphatic alcohol having 2-10 carbonatoms and 2-6 hydroxyl groups as dispersant/plasticizer for the starch ether | CARGILL B.V. (NL) | 1993-09-22 | — | — | EP | claimed |
| EP-0552879-A1 | Improved iontophoretic administration of drugs | MACROCHEM CORPORATION (US) | 1993-07-28 | — | — | EP | claimed |
| EP-0190104-B1 | MANUFACTURE OF HYDROLYSED MALEIC ANHYDRIDE POLYMERS | CIBA-GEIGY AG (CH) | 1990-01-24 | — | — | EP | claimed |
| US-4645619-A | Process for the preparation of colloidal dispersions of chalcogens and chalcogenide alloys | XEROX CORPORATION (US) | 1987-02-24 | — | — | US | claimed |
| EP-0074123-B1 | A PROCESS FOR PRODUCING A SINGLE CELL PROTEIN MATERIAL (SCP), SCP AND BIOLOGICALLY PURE CULTURE OF YEAST | PHILLIPS PETROLEUM COMPANY (US) | 1986-04-30 | — | — | EP | claimed |
| EP-0074123-A2 | A process for producing a single cell protein material (SCP), SCP and biologically pure culture of yeast | PHILLIPS PETROLEUM COMPANY (US) | 1983-03-16 | — | — | EP | claimed |