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 SCHEMBL27584009 | 1.00 | CA1 (0.89) | — | |
| Acetic Acid SCHEMBL38660000 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL1406132 | 0.95 | — | — | |
| Acetic Acid SCHEMBL28940968 | 0.95 | — | — | |
| Acetic Acid SCHEMBL21059110 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL8535873 | 0.95 | — | — | |
| Acetic Acid SCHEMBL3985386 | 0.95 | — | — | |
| Acetic Acid SCHEMBL3980080 | 0.95 | — | — | |
| Acetic Acid SCHEMBL2031116 | 0.95 | CA1 (0.80) | — | |
| Acetic Acid SCHEMBL21752845 | 0.95 | — | — |
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 9843 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-117683044-B | Preparation method and application of asymmetric diaryl trithiophene/selenophene small molecular material | UNIVERSITY OF CHINESE ACADEMY OF SCIENCES (CN) | 2026-05-26 | — | — | CN | claimed |
| CN-122080917-A | High stable CsMnBr3/ZrO2Method for preparing fluorescent film | — | 2026-05-26 | — | — | CN | claimed |
| CN-122076452-A | Fluidized bed catalyst and preparation method and application thereof | — | 2026-05-26 | — | — | CN | claimed |
| US-20260138881-A1 | METHOD FOR PRODUCING PHOTORESPONSIVE NANOPARTICLE WITH PEROVSKITE-TYPE CRYSTALLINE STRUCTURE | CANON KK (JP) | 2026-05-21 | — | — | US | claimed |
| CN-122059785-A | Method for preparing 1, 1-disubstituted alkene by rhodium-catalyzed decarboxylation cracking | 华南理工大学 | 2026-05-19 | — | — | CN | claimed |
| CN-122060491-A | Precursor system for perovskite nanocrystalline preparation, perovskite nanocrystalline and preparation method thereof | 西安交通大学 | 2026-05-19 | — | — | CN | claimed |
| CN-122059813-A | Synthesis method of 1, 1-diaryl ethylene | 南通大学 | 2026-05-19 | — | — | CN | claimed |
| CN-119592135-B | Perovskite ink composition, perovskite ink and preparation method thereof, perovskite film and preparation method and application thereof | 中国石油天然气集团有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-122035858-A | Preparation method of cesium acetate cooperated with nitrogen-doped lignin porous carbon material | 延边大学 | 2026-05-15 | — | — | CN | claimed |
| CN-122036583-A | Method for synthesizing gamma-lactam derivative by cobalt catalytic cyclization | 华南理工大学 | 2026-05-15 | — | — | CN | claimed |
| US-4203865-A | LEAD COMPOUND, ALKALI METAL COMPOUND, AND A HALOGENATED OLEFIN | PHILLIPS PETROLEUM COMPANY (US) | 1980-05-20 | — | — | US | claimed |
| US-4197253-A | FROM SYNTHESIS GAS USING A RHODIUM CARBONYL CATALY>T WITH A PHOSPHINE OXIDE PROMOTER | UNION CARBIDE CORPORATION (US) | 1980-04-08 | — | — | US | claimed |
| EP-0006634-A1 | Catalytic process for producing polyhydric alcohols | UNION CARBIDE CORPORATION (US) | 1980-01-09 | — | — | EP | claimed |
| US-4180676-A | Conversion of conjugated diolefins to diacyloxy olefins | PHILLIPS PETROLEUM COMPANY (US) | 1979-12-25 | — | — | US | claimed |
| US-4164615-A | USING AS CATALYST A TITANIUM COMPOUND, AN ALKALI METAL COMPOUND, AND A HALIDE | PHILLIPS PETROLEUM COMPANY (US) | 1979-08-14 | — | — | US | claimed |
| US-4159967-A | Catalyst for the oxidation of a conjugated diolefin | PHILLIPS PETROLEUM COMPANY (US) | 1979-07-03 | — | — | US | claimed |
| US-4152295-A | CATALYST FOR THE OXIDATION OF A CONJUGATED DIOLEFIN | PHILLIPS PETROLEUM COMPANY (US) | 1979-05-01 | — | — | US | claimed |
| US-4099018-A | REACTION WITH CARBOXY COMPOUND, CATALYTIC LEAD COMPOUND | PHILLIPS PETROLEUM COMPANY (US) | 1978-07-04 | — | — | US | claimed |
| US-4095037-A | BISMUTH COMPOUNDS, ALKALI METAL COMPOUNDS, NITRATES | PHILLIPS PETROLEUM COMPANY (US) | 1978-06-13 | — | — | US | claimed |
| US-4093815-A | REACTION WITH CARBOXYLIC ACID AND A CARBOXYLIC ACID ANHYDRIDE IN THE PRESENCE OF OXYGEN | PHILLIPS PETROLEUM COMPANY (US) | 1978-06-06 | — | — | US | claimed |