Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Acetic Acid. 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 | |
|---|---|---|---|---|
| Acetic Acid SCHEMBL28186565 | 1.00 | FFAR3 (0.78) | — | |
| Acetic Acid SCHEMBL6049138 | 1.00 | FFAR3 (0.78) | — | |
| Acetic Acid SCHEMBL15541200 | 0.95 | — | — | |
| Acetic Acid SCHEMBL7864469 | 0.95 | — | — | |
| Acetic Acid SCHEMBL28241189 | 0.95 | — | — | |
| Acetic Acid SCHEMBL27919102 | 0.95 | — | — | |
| Acetic Acid SCHEMBL29111482 | 0.95 | — | — | |
| Acetic Acid SCHEMBL28263940 | 0.95 | — | — | |
| Acetic Acid SCHEMBL895797 | 0.89 | — | — | |
| Acetic Acid SCHEMBL584739 | 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
Appears in 2148 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 |
|---|---|---|---|---|---|---|---|
| CN-121535204-B | Submicron spherical gold powder and preparation method thereof | CHANGCHUN GOLD RESEARCH INSTITUTE Co.,Ltd. (CN) | 2026-05-26 | — | — | CN | claimed |
| EP-4722204-A1 | INDUSTRIAL PREPARATION OF HETEROCYCLIC MODULATOR FOR LIPID SYNTHESIS | Sagimet Biosciences Inc. (US) | 2026-04-08 | — | — | EP | claimed |
| EP-4682154-A1 | PROTECTED TETRASACCHARIDES, THEIR PROCESS OF PREPARATION AND THEIR USE IN THE SYNTHESIS OF OLIGOSACCHARIDES REPRESENTING SEGMENTS OF O-ANTIGENS FROM DIVERSE SHIGELLA FLEXNERI SEROTYPES | Institut Pasteur (FR) | 2026-01-21 | — | — | EP | claimed |
| CN-114709337-B | Method for preparing lead-free tin-based perovskite film and solar cell thereof by using ionic salt to realize no antisolvent | 西北工业大学 | 2025-05-30 | — | — | CN | claimed |
| CN-120059255-A | High-solubility high-flame-retardance aromatic polyoxadiazole film and preparation method thereof | 烟台泰和新材高分子新材料研究院有限公司 | 2025-05-30 | — | — | CN | claimed |
| CN-120040523-A | Synthesis method of fondaparinux sodium intermediate D5 | 苏州莱克施德药业有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-119751521-A | Synthesis method of antitumor and antiangiogenic medicine PI-88 and precursor thereof | 陕西师范大学 | 2025-04-04 | — | — | CN | claimed |
| WO-2025060999-A1 | HDAC8 INHIBITOR, PREPARATION METHOD THEREFOR AND USE THEREOF | 浙江大学海南研究院 | 2025-03-27 | — | — | WO | claimed |
| CN-115974890-B | Lycorine derivative, preparation method thereof and application thereof in preparation of antitumor drugs | 山东达因海洋生物制药股份有限公司 | 2025-03-04 | — | — | CN | claimed |
| CN-119431470-A | Compound for preparing artificial tumor target and preparation method and application thereof | 中山大学·深圳 | 2025-02-14 | — | — | CN | claimed |
| EP-0918052-A1 | Improved polymeric mdi color | Bayer Corporation (US) | 1999-05-26 | — | — | EP | claimed |
| US-5597941-A | Process for production of 5-amino-3-methylpyrazole | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1997-01-28 | — | — | US | claimed |
| EP-0749448-A1 | ISOCYANATE-CROSSLINKED COATINGS HAVING REDUCED YELLOWING | OLIN CORPORATION (US) | 1996-12-27 | — | — | EP | claimed |
| EP-0749448-A4 | ISOCYANATE-CROSSLINKED COATINGS HAVING REDUCED YELLOWING | OLIN CORP (US) | 1996-06-19 | — | — | EP | claimed |
| WO-1995006674-A1 | ISOCYANATE-CROSSLINKED COATINGS HAVING REDUCED YELLOWING | OLIN CORPORATION (US) | 1995-03-09 | — | — | WO | claimed |
| US-5371203-A | Reacting a triester of L-fucose with trichloroacetonitrile to form corresponding trichloroacetimidate, followed by phosphating,hydrogenolysis, deprotecting, salt formation; a substrate for fucosyltransferases; tumor diagnosis | MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) | 1994-12-06 | — | — | US | claimed |
| US-5101026-A | GANGLIOSIDE RELATED COMPOUNDS AND METHOD OF PRODUCING THE SAME | MECT CORPORATION (JP) | 1992-03-31 | — | — | US | claimed |
| US-4968786-A | INTERMEDIATES FOR GANGLIOSIDES | RIKAGAKU KENKYUSHO (JP) | 1990-11-06 | — | — | US | claimed |
| EP-0255717-A2 | Ganglioside related compounds and method of producing the same | MECT CORPORATION (JP) | 1988-02-10 | — | — | EP | claimed |
| EP-0166442-A2 | Sialic acid derivatives, galactose derivatives and method for producing the same | RIKAGAKU KENKYUSHO (JP) | 1986-01-02 | — | — | EP | claimed |