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 SCHEMBL28385300 | 1.00 | LMNA (0.80) | — | |
| Acetic Acid SCHEMBL27827411 | 1.00 | LMNA (0.80) | — | |
| Acetic Acid SCHEMBL27827814 | 0.95 | — | — | |
| Acetic Acid SCHEMBL7766504 | 0.95 | LMNA (0.73) | — | |
| Acetic Acid SCHEMBL27799892 | 0.95 | — | — | |
| Acetic Acid SCHEMBL16196241 | 0.95 | LMNA (0.73) | — | |
| Acetic Acid SCHEMBL27645349 | 0.95 | — | — | |
| Acetic Acid SCHEMBL18979653 | 0.95 | LMNA (0.73) | — | |
| Acetic Acid SCHEMBL18979632 | 0.95 | LMNA (0.73) | — | |
| Acetic Acid SCHEMBL7867974 | 0.91 | LMNA (0.67) | — |
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 122 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-104447389-A | Method for preparing specified impurity in ethylenediamine diaceturate | LIAONING COTECH BIO GENE PHARMACEUTICAL CO LTD | 2015-03-25 | — | — | CN | claimed |
| CN-103245740-A | Related substance of ethylenediamine diaceturate and detection method thereof | LIAONING COTECH BIO GEN PHARMACEUTICAL CO LTD | 2013-08-14 | — | — | CN | claimed |
| CN-102180879-B | Polycrystalline type alpha acetic acid solvate of hypnotic | INST RADIATION MED AMMS PLA | 2013-05-01 | — | — | CN | claimed |
| CN-102180879-A | Polycrystalline type alpha acetic acid solvate of hypnotic | INST RADIATION MED AMMS PLA | 2011-09-14 | — | — | CN | claimed |
| CN-101124216-A | Heterocyclic MCHr1 antagonists and their use in therapy | ASTRAZENECA AB (SE) | 2008-02-13 | — | — | CN | claimed |
| EP-1747206-A1 | AMINO-TETRAZOLES ANALOGUES AND METHODS OF USE | ABBOTT LABORATORIES (US) | 2007-01-31 | — | — | EP | claimed |
| WO-2005111003-A1 | AMINO-TETRAZOLES ANALOGUES AND METHODS OF USE | ABBOTT LABORATORIES (US) | 2005-11-24 | — | — | WO | claimed |
| EP-4504880-B1 | WATER BASED SEMI-SYNTHETIC METAL WORKING FLUID COMPOSITION CONTAINING A CYCLIC POLYFUNCTIONAL AMINE | DOW GLOBAL TECHNOLOGIES LLC (US) | 2025-11-19 | — | — | EP | disclosed |
| US-12410376-B2 | Water based semi-synthetic metal working fluid composition containing an alkyl alcohol amine | DOW GLOBAL TECHNOLOGIES LLC (US) | 2025-09-09 | — | — | US | disclosed |
| US-12364262-B2 | Water based semi-synthetic metal working fluid composition containing an aminopropenediol | DOW GLOBAL TECHNOLOGIES LLC (US) | 2025-07-22 | — | — | US | disclosed |
| CN-120148841-A | Pulmonary nodule malignant risk prediction system based on exhaled gas VOCs | 江苏瑞质生物科技有限公司 | 2025-06-13 | — | — | CN | disclosed |
| US-20250179059-A1 | ANTICANCER COMPOUNDS | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2025-06-05 | — | — | US | disclosed |
| US-20250059457-A1 | WATER BASED SEMI-SYNTHETIC METAL WORKING FLUID COMPOSITION CONTAINING AN ALKYL ALCOHOL AMINE | DOW GLOBAL TECHNOLOGIES LLC (US) | 2025-02-20 | — | — | US | disclosed |
| US-4564477-A | DOLICHOL INTERMEDIATE | KURARAY CO., LTD. (JP) | 1986-01-14 | — | — | US | disclosed |
| EP-0087136-B1 | NOVEL POLYPRENYL COMPOUNDS, METHOD OF PRODUCING THE SAME AND THEIR USE IN DOLICHOL PRODUCTION | KURARAY CO., LTD. (JP) | 1985-07-31 | — | — | EP | disclosed |
| US-4495322-A | CONDENSED PARTIALLY HYDROLZED SILOXANES AND AN AMIDE, CARBAMIC ACID ESTER, OR UREA | ROHM GMBH (DE) | 1985-01-22 | — | — | US | disclosed |
| US-4473704-A | ANALGESICS, ANTIEMETICS | PFIZER INC. (US) | 1984-09-25 | — | — | US | disclosed |
| EP-0090526-A1 | Substituted dodecahydrotriphenylenes, decahydro-1H-cyclopenta(1)phenanthrenes, decahydro-1H-pyrido(1,2-f)phenanthridines and decahydropyrrolo(1,2-f)phenanthridines as CNS agents | PFIZER INC. (US) | 1983-10-05 | — | — | EP | disclosed |
| EP-0087136-A2 | Novel polyprenyl compounds, method of producing the same and their use in dolichol production | KURARAY CO., LTD. (JP) | 1983-08-31 | — | — | EP | disclosed |
| US-4111923-A | LUTEINIZING HORMONE RELEASING FACTOR ANTAGONISTS | PARKE, DAVIS & COMPANY (US) | 1978-09-05 | — | — | US | disclosed |