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.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA1 | P00915 | 2/20 | 0.80 |
| ▸ | CA4 | P22748 | 3/20 | 0.54 |
| ▸ | LMNA | P02545 | 2/20 | 0.46 |
| ▸ | TSHR | P16473 | 2/20 | 0.42 |
| ▸ | FFAR3 | O14843 | 2/20 | 0.42 |
| ▸ | THPO | P40225 | 1/20 | 0.42 |
| ▸ | LCK | P06239 | 1/20 | 0.42 |
| ▸ | FYN | P06241 | 1/20 | 0.42 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.39 |
| ▸ | BLM | P54132 | 1/20 | 0.39 |
| ▸ | PMP22 | Q01453 | 1/20 | 0.39 |
| ▸ | FAHD1 | Q6P587 | 1/20 | 0.39 |
| ▸ | CES1 | P23141 | 1/20 | 0.35 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.33 |
| ▸ | HDAC3 | O15379 | 1/20 | 0.33 |
| ▸ | HDAC1 | Q13547 | 1/20 | 0.33 |
| ▸ | HDAC2 | Q92769 | 1/20 | 0.33 |
| ▸ | HDAC8 | Q9BY41 | 1/20 | 0.33 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.33 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.33 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 SCHEMBL5186280 | 1.00 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL28716621 | 1.00 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL95353 | 1.00 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL1024877 | 0.95 | CA1 (0.89) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL25170206 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL25312642 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL21752953 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL25215531 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL20720790 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 | |
| Acetic Acid SCHEMBL21848043 | 0.90 | CA1 (0.80) | CA1CA4LMNATSHRFFAR3 |
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 60 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117434258-A | Two-dimensional adjustable pore plate sample support and application thereof in detection of prostate antigen | 浙江工业大学 | 2024-01-23 | — | — | CN | claimed |
| CN-108148596-A | A kind of method for differentiating red wine using upconverting fluorescent material fluorescence quenching | 天津科技大学 | 2018-06-12 | — | — | CN | claimed |
| CN-105713613-B | A kind of conversion of solar cell light rear-earth-doped quanta point material and its preparation | 华南理工大学 | 2018-02-27 | — | — | CN | claimed |
| CN-105713613-A | Rare earth doped quantum dot material for light conversion of solar cells and preparation of rare earth doped quantum dot material | 华南理工大学 | 2016-06-29 | — | — | CN | claimed |
| EP-2655482-A1 | POLYHETEROSILOXANE COMPOSITION INCLUDING LANTHANIDE METAL | Dow Corning Corporation (US) | 2013-10-30 | — | — | EP | claimed |
| CN-103354823-A | Polyheterosiloxane composition including lanthanide metal | DOW CORNING | 2013-10-16 | — | — | CN | claimed |
| WO-2012088439-A1 | POLYHETEROSILOXANE COMPOSITION INCLUDING LANTHANIDE METAL | DOW CORNING CORPORATION (US) | 2012-06-28 | — | — | WO | claimed |
| US-12529154-B2 | Electrode for electrolysis | LG CHEM, LTD. (KR) | 2026-01-20 | — | — | US | disclosed |
| WO-2025121735-A1 | PHARMACEUTICAL COMPOSITION COMPRISING UPCONVERSION NANOPARTICLES FOR PREVENTING OR TREATING CANCER | 부산대학교 산학협력단 | 2025-06-12 | — | — | WO | disclosed |
| US-20250122424-A1 | LOW PHONON ENERGY NANOPARTICLES BASED ON ALKALI LEAD HALIDES AND METHODS OF SYNTHESIS AND USE | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2025-04-17 | — | — | US | disclosed |
| WO-2024237543-A1 | MULTI-FUNCTIONAL PARTICLES FOR NEAR-INFRARED IMAGING GUIDANCE AND PHOTOTHERMAL THERAPY AND COMPOSITE COMPRISING SAME | 한양대학교 산학협력단 | 2024-11-21 | — | — | WO | disclosed |
| CN-114008248-B | Electrode for electrolysis | 株式会社LG化学 | 2024-09-27 | — | — | CN | disclosed |
| EP-3971327-B1 | ELECTRODE FOR ELECTROLYSIS | LG CHEMICAL LTD (KR) | 2024-06-19 | — | — | EP | disclosed |
| WO-2009005670-A2 | MIXED METAL OXIDE CATALYSTS FOR THE AMMOXIDATION OF PROPANE AND ISOBUTANE | INEOS USA LLC (US) | 2009-01-08 | — | — | WO | disclosed |
| US-20090005586-A1 | MIXED METAL OXIDE CATALYSTS FOR THE AMMOXIDATION OF PROPANE AND ISOBUTANE | INEOS USA LLC | 2009-01-01 | — | — | US | disclosed |
| US-20080200716-A1 | Mixed metal oxide catalysts for the ammoxidation of propane and isobutane | INEOS USA LLC | 2008-08-21 | — | — | US | disclosed |
| US-20080200715-A1 | PROCESS FOR THE AMMOXIDATION OF PROPANE AND ISOBUTANE | INEOS USA LLC | 2008-08-21 | — | — | US | disclosed |
| US-20080103325-A1 | Mixed metal oxide catalysts for the ammoxidation of propane and isobutane | INEOS USA LLC | 2008-05-01 | — | — | US | disclosed |
| US-20080103326-A1 | Consistent performance; high yield gas phase conversion to acrylonitrile and methacrylonitrile; includes molybdenum, vanadium, antimony, niobium, lanthanides with titanium, tin, germanium, zirconium and/or hafnium | INEOS USA LLC | 2008-05-01 | — | — | US | disclosed |
| WO-2007104359-A1 | SYNTHESIS OF AMINES WITH YTTERBIUM LEWIS ACIDS | JACOBS UNIVERSITY BREMEN GGMBH (DE) | 2007-09-20 | — | — | WO | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-12529154-B2 | Electrode for electrolysis | EZH2, TPO, PRDM7 | CA1 6/4885CA4 118/4885LMNA 3138/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.