Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Allyl Alcohol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| Allyl Alcohol SCHEMBL29032342 | 0.94 | TSHR (0.53) | — | |
| Allyl Alcohol SCHEMBL28443676 | 0.91 | TSHR (0.50) | — | |
| Allyl Alcohol SCHEMBL465193 | 0.86 | — | — | |
| Allyl Alcohol SCHEMBL27117738 | 0.86 | TSHR (0.69) | — | |
| Methacrylic Acid SCHEMBL7167987 | 0.85 | TSHR (0.50) | — | |
| Allyl Alcohol SCHEMBL27500481 | 0.82 | — | — | |
| Propionic Acid SCHEMBL28368538 | 0.81 | — | — | |
| Acetic Acid SCHEMBL9815980 | 0.80 | — | — | |
| Allyl Alcohol SCHEMBL7058473 | 0.80 | — | — | |
| Acetic Acid SCHEMBL11750370 | 0.80 | FFAR3 (0.47) | — |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120058585-A | Dimercapto conjugate of active allyl alcohol acetate, and preparation method and application thereof | 南京工业大学 | 2025-05-30 | — | — | CN | claimed |
| US-5047441-A | Rigid polyurethane foams prepared from polyvinyl acetate/allyl alcohol polyols, and process for making same | BASF CORPORATION (US) | 1991-09-10 | — | — | US | claimed |
| CN-120058585-A | Dimercapto conjugate of active allyl alcohol acetate, and preparation method and application thereof | 南京工业大学 | 2025-05-30 | — | — | CN | disclosed |
| CN-120058585-A | Dimercapto conjugate of active allyl alcohol acetate, and preparation method and application thereof | 南京工业大学 | 2025-05-30 | — | — | CN | disclosed |
| CN-120058585-A | Dimercapto conjugate of active allyl alcohol acetate, and preparation method and application thereof | 南京工业大学 | 2025-05-30 | — | — | CN | disclosed |
| CN-117700299-A | Preparation method of allyl alcohol | 上海优铖工逸技术有限公司 | 2024-03-15 | — | — | CN | disclosed |
| CN-111129583-B | Gel electrolyte and preparation method of lithium ion battery containing gel electrolyte | 河南电池研究院有限公司 | 2022-12-13 | — | — | CN | disclosed |
| CN-114874140-A | Cyclic imine derivative with acrylate structure and preparation method thereof | 吉林大学 | 2022-08-09 | — | — | CN | disclosed |
| CN-110117365-B | Modified polymethylsiloxane, modified high-cis conjugated diene polymer, method for producing same, rubber composition, and tire | 奇美实业股份有限公司 | 2021-12-14 | — | — | CN | disclosed |
| CN-111992248-B | Catalyst for oxidation esterification of isobutene, preparation method and application thereof | 北京水木滨华科技有限公司 | 2021-07-23 | — | — | CN | disclosed |
| CN-111992248-A | Catalyst for oxidation esterification of isobutene, preparation method and application thereof | 北京水木滨华科技有限公司 | 2020-11-27 | — | — | CN | disclosed |
| US-4939221-A | Polyvinyl acetate/allyl alcohol copolymers | BASF CORPORATION (US) | 1990-07-03 | — | — | US | disclosed |
| US-4939221-A | Polyvinyl acetate/allyl alcohol copolymers | BASF CORPORATION (US) | 1990-07-03 | — | — | US | disclosed |
| US-4939221-A | Polyvinyl acetate/allyl alcohol copolymers | BASF CORPORATION (US) | 1990-07-03 | — | — | US | disclosed |
| EP-0140254-B1 | PROCESS FOR THE PREPARATION OF FLUORALKYL-SUBSTITUTED IODOALKANES | HOECHST AKTIENGESELLSCHAFT (DE) | 1988-10-05 | — | — | EP | disclosed |
| EP-0231287-A1 | WATER-BASED FUNCTIONAL FLUID THICKENING COMBINATIONS OF SURFACTANTS AND HYDROCARBYL-SUBSTITUTED SUCCINIC ACID AND/OR ANHYDRIDE/AMINE TERMINATED POLY(OXYALKYLENE) REACTION PRODUCTS. | LUBRIZOL CORP (US) | 1987-08-12 | — | — | EP | disclosed |
| WO-1987000856-A1 | WATER-BASED FUNCTIONAL FLUID THICKENING COMBINATIONS OF SURFACTANTS AND HYDROCARBYL-SUBSTITUTED SUCCINIC ACID AND/OR ANHYDRIDE/AMINE TERMINATED POLY(OXYALKYLENE) REACTION PRODUCTS | THE LUBRIZOL CORPORATION (US) | 1987-02-12 | — | — | WO | disclosed |
| US-4587366-A | HALOALKYLATION, METAL CATALYSTS | HOECHST AKTIENGESELLSCHAFT (DE) | 1986-05-06 | — | — | US | disclosed |
| EP-0142041-A1 | Process for the preparation of fluoralkyl-substituted alkanes or alkenes | HOECHST AKTIENGESELLSCHAFT (DE) | 1985-05-22 | — | — | EP | disclosed |
| EP-0140254-A1 | Process for the preparation of fluoralkyl-substituted iodoalkanes | HOECHST AKTIENGESELLSCHAFT (DE) | 1985-05-08 | — | — | EP | disclosed |