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 SCHEMBL29939184 | 1.00 | FFAR3 (0.54) | — | |
| Acetic Acid SCHEMBL3278799 | 0.96 | — | — | |
| Acetic Acid SCHEMBL28224614 | 0.96 | — | — | |
| Acetic Acid SCHEMBL28546925 | 0.87 | FFAR3 (0.41) | — | |
| Bicarbonate SCHEMBL4925614 | 0.84 | — | — | |
| Bicarbonate SCHEMBL5172813 | 0.84 | CA1 (0.46) | — | |
| Acetic Acid SCHEMBL27640276 | 0.83 | FFAR3 (0.37) | — | |
| Oxalic Acid SCHEMBL29242678 | 0.80 | — | — | |
| Acetic Acid SCHEMBL29913812 | 0.80 | — | — | |
| Acetic Acid SCHEMBL4942868 | 0.80 | FFAR3 (0.58) | — |
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 6836 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 |
|---|---|---|---|---|---|---|---|
| EP-4741372-A1 | USE OF ADDITIVE, FORMAMIDINIUM IODIDE AND PREPARATION METHOD THEREFOR, PEROVSKITE SOLAR CELL, SOLAR POWER GENERATION DEVICE, AND ELECTRIC DEVICE | Contemporary Amperex Technology Co., Limited (CN) | 2026-05-13 | — | — | EP | claimed |
| CN-122006803-A | Preparation method and application of two-dimensional multilayer D-J halide perovskite | 华东理工大学 | 2026-05-12 | — | — | CN | claimed |
| US-20260116849-A1 | APPLICATION OF ADDITIVE, FORMAMIDINIUM IODIDE AND PREPARATION METHOD THEREFOR, PEROVSKITE SOLAR CELL, SOLAR POWER GENERATION APPARATUS, AND ELECTRICAL APPARATUS | CONTEMPORARY AMPEREX TECHNOLOGY CO LTD (CN) | 2026-04-30 | — | — | US | claimed |
| US-12604651-B2 | Rapid fabrication of semiconductor thin films | MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) | 2026-04-14 | — | — | US | claimed |
| CN-121574070-A | Synthesis method of high-purity super-crystal formamidine bromide (FABr) | 苏州优选新能源科技有限公司 | 2026-02-27 | — | — | CN | claimed |
| EP-4679984-A1 | PHOTOELECTRIC CONVERSION ELEMENT | Enecoat Technologies Co., Ltd. (JP) | 2026-01-14 | — | — | EP | claimed |
| US-12428426-B2 | Process and intermediates for preparing a JAK1 inhibitor | INCYTE CORPORATION (US) | 2025-09-30 | — | — | US | claimed |
| US-12364156-B2 | Method for making a perovskite layer at high speed | ENERGY MATERIALS CORPORATION (US) | 2025-07-15 | — | — | US | claimed |
| US-12349584-B2 | Organic-inorganic perovskite solar cell with directional arrangement of intrinsic perovskite dipoles and preparation method thereof | SHANDONG UNIVERSITY (CN) | 2025-07-01 | — | — | US | claimed |
| CN-113227058-B | Improved process for preparing 4, 6-dihydroxypyrimidine | 赛拓有限责任公司 | 2025-06-24 | — | — | CN | claimed |
| WO-1996027572-A1 | METHODS AND COMPOSITIONS FOR ENHANCING FORMYLTETRAHYDROPTEROYLPOLYGLUTAMATE IN PLANTS | NONOMURA ARTHUR M (US) | 1996-09-12 | — | — | WO | claimed |
| EP-0486385-B1 | Imidazole derivatives, process for their fabrication and pharmaceutical compositions containing them | ADIR (FR) | 1994-12-28 | — | — | EP | claimed |
| EP-0325892-B1 | PROCESS FOR THE PREPARATION OF HALOGENATED PRIMARY AMINES | CIBA-GEIGY AG (CH) | 1993-02-03 | — | — | EP | claimed |
| EP-0293063-B1 | 2-PHENYLPURINONE DERIVATIVES, PROCESSES FOR THEIR PREPARATION, AND THEIR USE AS WELL AS INTERMEDIATES | SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) | 1992-03-18 | — | — | EP | claimed |
| US-4960936-A | Process for the preparation of halogenated aromatic primary amines | CIBA-GEIGY CORPORATION (US) | 1990-10-02 | — | — | US | claimed |
| EP-0293063-A1 | 2-Phenylpurinone derivatives, processes for their preparation, and their use as well as intermediates | SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) | 1988-11-30 | — | — | EP | claimed |
| EP-0124961-B1 | A PROCESS FOR THE PRODUCTION OF 4-CARBAMOYL-1H-IMIDAZOLIUM-5-OLATE | WARNER-LAMBERT COMPANY (US) | 1987-12-09 | — | — | EP | claimed |
| US-4503235-A | Process for producing 4-carbamoyl-1H-imidazolium-5-olate | WARNER-LAMBERT COMPANY (US) | 1985-03-05 | — | — | US | claimed |
| EP-0124961-A2 | A process for the production of 4-carbamoyl-1H-imidazolium-5-olate | WARNER-LAMBERT COMPANY (US) | 1984-11-14 | — | — | EP | claimed |
| US-4267324-A | BY REACTION OF FORMAMIDINE AND 3-AMINO-4-CYANOPYRAZOLE | POLAROID CORPORATION (US) | 1981-05-12 | — | — | US | claimed |