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 SCHEMBL4317432 | 0.94 | — | — | |
| Acetic Acid SCHEMBL5855458 | 0.94 | — | — | |
| Acetic Acid SCHEMBL29217338 | 0.94 | — | — | |
| Acetic Acid SCHEMBL1674512 | 0.94 | FFAR3 (1.00) | — | |
| Acetic Acid SCHEMBL1331719 | 0.94 | — | — | |
| Acetic Acid SCHEMBL11142541 | 0.94 | FFAR3 (1.00) | — | |
| Acetic Acid SCHEMBL7472549 | 0.94 | — | — | |
| Acetic Acid SCHEMBL1330415 | 0.94 | — | — | |
| Acetic Acid SCHEMBL41073 | 0.94 | FFAR3 (1.00) | — | |
| Acetic Acid SCHEMBL6788 | 0.94 | FFAR3 (1.00) | — |
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 744 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122039125-A | Wood-derived carbon self-supporting transition metal core-shell hydrogen evolution catalyst and preparation method thereof | 广西大学 | 2026-05-15 | — | — | CN | claimed |
| CN-120015826-A | Medium-entropy manganese-based phosphate sodium-electricity positive electrode material, and preparation method and application thereof | 武汉纺织大学 | 2025-05-16 | — | — | CN | claimed |
| CN-120004697-A | Preparation method of OrgVO material and application of OrgVO material as secondary battery anode material | 同济大学 | 2025-05-16 | — | — | CN | claimed |
| CN-119736089-B | Fluoride scintillation crystal doped with rare earth ions and preparation method thereof | 中国计量大学 | 2025-05-09 | — | — | CN | claimed |
| CN-119736089-A | Fluoride scintillation crystal doped with rare earth ions and preparation method thereof | 中国计量大学 | 2025-04-01 | — | — | CN | claimed |
| CN-119663252-A | Component-adjustable rare earth oxide coating and preparation method thereof | 华中科技大学 | 2025-03-21 | — | — | CN | claimed |
| CN-119433594-A | Lignin derived carbon-alloy-metal oxide heterojunction catalyst and preparation method thereof | 广西大学 | 2025-02-14 | — | — | CN | claimed |
| CN-119259066-A | Ethylbenzene dehydrogenation catalyst and preparation method and application thereof | 中国石油化工股份有限公司 | 2025-01-07 | — | — | CN | claimed |
| CN-119118152-A | Molecular sieves BUCT-10, their synthesis and use | 北京化工大学 | 2024-12-13 | — | — | CN | claimed |
| CN-118956395-A | 365Nm excited blue-violet fluorescent powder with high thermal stability and preparation method thereof | 陕西学前师范学院 | 2024-11-15 | — | — | CN | claimed |
| CN-101260217-B | Composite pyroelectricity material, preparation method thereof, and method for preparing silicon-base thick film | UNIV HUAZHONG SCIENCE TECH | 2010-10-13 | — | — | CN | claimed |
| CN-101824154-A | Preparation method of carboxylated lignin | BEIJING GHEMU TECHNOLOGY CO LTD | 2010-09-08 | — | — | CN | claimed |
| US-7651674-B2 | uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes; forming core-shell structure; useful to form a luminescent layer of an inorganic-organic hybrid electroluminescence device | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2010-01-26 | — | — | US | claimed |
| US-20080297044-A1 | uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes; forming core-shell structure; useful to form a luminescent layer of an inorganic-organic hybrid electroluminescence device | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2008-12-04 | — | — | US | claimed |
| US-7455825-B2 | uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes; forming core-shell structure; useful to form a luminescent layer of an inorganic-organic hybrid electroluminescence device | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2008-11-25 | — | — | US | claimed |
| CN-101260217-A | Composite pyroelectricity material, preparation method thereof, and method for preparing silicon-base thick film | UNIV HUAZHONG SCIENCE TECH (CN) | 2008-09-10 | — | — | CN | claimed |
| US-20060039850-A1 | uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes; forming core-shell structure; useful to form a luminescent layer of an inorganic-organic hybrid electroluminescence device | SAMSUNG ELECTRONICS CO., LTD. (KR) | 2006-02-23 | — | — | US | claimed |
| US-6916963-B2 | Process using water tolerant Lewis acids in catalytic hydration of alkylene oxides to alkylene glycols | SAUDI BASIC INDUSTRIES CORPORATION (SA) | 2005-07-12 | — | — | US | claimed |
| US-20050014980-A1 | Process using water tolerant lewis acids in catalytic hydration of alkylene oxides to alkylene glycols | SAUDI BASIC INDUSTRIES CORPORATION | 2005-01-20 | — | — | US | claimed |
| US-5049630-A | Food and beverage container, polycarbonyls | SHELL OIL COMPANY (US) | 1991-09-17 | — | — | US | claimed |