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 SCHEMBL16566845 | 0.96 | — | — | |
| Acetic Acid SCHEMBL21817930 | 0.92 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL31365285 | 0.84 | FFAR3 (0.54) | — | |
| Bicarbonate SCHEMBL18244694 | 0.80 | CA1 (0.56) | — | |
| Acetic Acid SCHEMBL31214327 | 0.80 | — | — | |
| Acetic Acid SCHEMBL28221982 | 0.80 | — | — | |
| Bicarbonate SCHEMBL225842 | 0.80 | — | — | |
| Acetic Acid SCHEMBL1330415 | 0.80 | — | — | |
| Acetic Acid SCHEMBL8742314 | 0.80 | FFAR3 (1.00) | — | |
| Acetic Acid SCHEMBL7472549 | 0.80 | — | — |
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 34 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114072389-B | Composition of 5-fluorouracil and refining method thereof | 上海旭东海普药业有限公司 | 2023-09-08 | — | — | CN | claimed |
| CN-109852441-A | A kind of polycyclic high-density biology matter liquid fuel and the preparation method and application thereof | 陕西理工大学 | 2019-06-07 | — | — | CN | claimed |
| CN-108352441-A | Polymer composition comprising ionic dipoles | 沙特基础工业全球技术公司 | 2018-07-31 | — | — | CN | claimed |
| US-6468331-B2 | PERMSELECTIVITY OF ALKENES OVER ALKANES UNDER DRY CONDITIONS; POUROUS SUPPORT; POLYMER ELECTROLYTE LAYER HAS METAL SALT; STABILITY | KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) | 2002-10-22 | — | — | US | claimed |
| US-20010013273-A1 | Solid state facilitated transport separation membranes using polymer electrolytes for alkene separation | KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) | 2001-08-16 | — | — | US | claimed |
| US-20250308806-A1 | ELECTROLYTIC CAPACITOR | PANASONIC INTELLECTUAL PROPERTY MANAGEMENT CO., LTD. (JP) | 2025-10-02 | — | — | US | disclosed |
| US-20250308805-A1 | ELECTROLYTIC CAPACITOR | PANASONIC INTELLECTUAL PROPERTY MANAGEMENT CO., LTD. (JP) | 2025-10-02 | — | — | US | disclosed |
| CN-114072389-B | Composition of 5-fluorouracil and refining method thereof | 上海旭东海普药业有限公司 | 2023-09-08 | — | — | CN | disclosed |
| CN-109852441-A | A kind of polycyclic high-density biology matter liquid fuel and the preparation method and application thereof | 陕西理工大学 | 2019-06-07 | — | — | CN | disclosed |
| CN-106687449-B | A kind of aminosulfonyl base class compound, preparation method and the usage | 苏州旺山旺水生物医药有限公司 | 2019-04-09 | — | — | CN | disclosed |
| CN-108352441-A | Polymer composition comprising ionic dipoles | 沙特基础工业全球技术公司 | 2018-07-31 | — | — | CN | disclosed |
| US-20180153860-A1 | METHODS OF DOSE ADMINISTRATION FOR TREATING OR PREVENTING COGNITIVE IMPAIRMENT USING INDANE ACETIC ACID DERIVATIVES | T3D THERAPEUTICS, INC. (US) | 2018-06-07 | — | — | US | disclosed |
| CN-1860117-A | Benzimidazole, benzthiazole and benzoxazole derivatives and their use as lta4h modulators | JANSSEN PHARMACEUTICA NV (BE) | 2006-11-08 | — | — | CN | disclosed |
| US-20060084680-A1 | Indane acetic acid derivatives and their use as pharmaceutical agents, intermediates, and method of preparation | BAYER PHARMACEUTICALS CORPORATION (US) | 2006-04-20 | — | — | US | disclosed |
| US-6468331-B2 | PERMSELECTIVITY OF ALKENES OVER ALKANES UNDER DRY CONDITIONS; POUROUS SUPPORT; POLYMER ELECTROLYTE LAYER HAS METAL SALT; STABILITY | KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) | 2002-10-22 | — | — | US | disclosed |
| US-20010013273-A1 | Solid state facilitated transport separation membranes using polymer electrolytes for alkene separation | KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) | 2001-08-16 | — | — | US | disclosed |
| US-5283357-A | Precipitating acid addition salt | MITSUI TOATSU CHEMICALS, INCORPORATED (JP) | 1994-02-01 | — | — | US | disclosed |
| US-4958029-A | Process for the production of isoindoline derivatives, novel intermediates and process for their production | BANYU PHARMACEUTICAL CO., LTD. (JP) | 1990-09-18 | — | — | US | disclosed |
| EP-0275064-A2 | Process for the production of isoindoline derivatives, novel intermediates and process for their production | Banyu Pharmaceutical Co., Ltd. (JP) | 1988-07-20 | — | — | EP | disclosed |
| US-4490449-A | CELL HAVING A METHYL SUBSTITUTED DIOXOLANE ELCETROLYTE SOLVENT | DURACELL INC. (US) | 1984-12-25 | — | — | US | disclosed |