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 SCHEMBL1880063 | 1.00 | CA1 (0.89) | — | |
| Acetic Acid SCHEMBL118599 | 1.00 | CA1 (0.89) | — | |
| Acetic Acid SCHEMBL1080 | 1.00 | — | — | |
| Acetic Acid SCHEMBL20272818 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL4019924 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL1367765 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL8761316 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL10797524 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL10602749 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL359080 | 0.95 | CA1 (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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115403631-B | Antitumor compound and preparation method and application thereof | 中国计量大学 | 2025-04-11 | — | — | CN | claimed |
| EP-3649663-B1 | METHOD FOR PREPARING AN ELECTRODE COMPRISING A SUBSTRATE, ALIGNED CARBON NANOTUBES AND A METAL OXIDE DEPOSITED BY OXIDATIVE DEPOSITION, THE ELECTRODE AND USES THEREOF. | COMMISSARIAT ENERGIE ATOMIQUE (FR) | 2024-08-28 | — | — | EP | claimed |
| EP-1127886-B1 | Synthesis of 3,6-dialkyl-5,6-dihydro-4-hydroxy-2H-pyran-2one | HOFFMANN LA ROCHE (CH) | 2003-05-07 | — | — | EP | claimed |
| EP-0245959-A2 | Ruthenium-phosphine complexes | Takasago Perfumery Co., Ltd. (JP) | 1987-11-19 | — | — | EP | claimed |
| CN-115403631-B | Antitumor compound and preparation method and application thereof | 中国计量大学 | 2025-04-11 | — | — | CN | disclosed |
| CN-119433582-A | Preparation method and application of nitrogen-doped porous carbon supported metal catalyst | 六盘水师范学院 | 2025-02-14 | — | — | CN | disclosed |
| CN-116891838-B | Alkene reductase mutant, composition, biological material and application thereof | 瑞博(苏州)制药有限公司 | 2023-11-28 | — | — | CN | disclosed |
| CN-117105890-A | Amide derivative, preparation method thereof and application thereof in medicine | 成都百裕制药股份有限公司 | 2023-11-24 | — | — | CN | disclosed |
| CN-116891838-A | Alkene reductase mutant, composition, biological material and application thereof | 瑞博(苏州)制药有限公司 | 2023-10-17 | — | — | CN | disclosed |
| CN-116804018-A | Amide derivative, preparation method thereof and application thereof in medicine | 成都百裕制药股份有限公司 | 2023-09-26 | — | — | CN | disclosed |
| CN-112538010-B | Preparation method of artemisinin compound synthesized key intermediate | 凯特立斯（深圳）科技有限公司 | 2023-08-11 | — | — | CN | disclosed |
| WO-2022237781-A1 | AMIDE DERIVATIVE AND APPLICATION THEREOF | 成都百裕制药股份有限公司 | 2022-11-17 | — | — | WO | disclosed |
| CN-102070383-A | Method for preparing 1,2-diketone by performing catalytic oxidation on olefin | UNIV SUZHOU | 2011-05-25 | — | — | CN | disclosed |
| EP-0453205-B1 | Process for producing polyolefin | TOSOH CORP (JP) | 1995-06-28 | — | — | EP | disclosed |
| EP-0453205-A2 | Process for producing polyolefin | Tosoh Corporation (JP) | 1991-10-23 | — | — | EP | disclosed |
| EP-0030214-B1 | PROCESS FOR THE PREPARATION OF 2,3,5,6-TETRACHLOROPYRIDINE AND 3,5,6-TRICHLOROPYRIDIN-2-OL | CIBA-GEIGY AG (CH) | 1985-01-30 | — | — | EP | disclosed |
| EP-0084328-A2 | Halogen alkyl substituted cyclopropanecarboxylic acid esters, process for their preparation and their use as insecticides | BAYER AG (DE) | 1983-07-27 | — | — | EP | disclosed |
| US-4284821-A | Dichlorovinylcyclobutanones, processes for preparing them, and their use as intermediates for producing pesticidal compositions | CIBA-GEIGY CORPORATION (US) | 1981-08-18 | — | — | US | disclosed |
| EP-0030214-A2 | Process for the preparation of 2,3,5,6-tetrachloropyridine and 3,5,6-trichloropyridin-2-ol | CIBA-GEIGY AG (CH) | 1981-06-10 | — | — | EP | disclosed |
| US-4245098-A | BY REACTING TRICHLOROACETALDEHYDE WITH ACRYLONITRILE | CIBA-GEIGY CORPORATION (US) | 1981-01-13 | — | — | US | disclosed |