Acetic Acid

Acetic Acid

SCHEMBL989871

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[BH4-].[Na+].[Na+].[Na+].[Na+]

nearest known ligand 0.90

Full drug profile on Sugi Atlas →

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)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.90
CA4 P22748 4/20 0.61
FAHD1 Q6P587 1/20 0.50
LMNA P02545 3/20 0.46
FFAR3 O14843 2/20 0.42
TSHR P16473 1/20 0.42
THPO P40225 1/20 0.42
LCK P06239 1/20 0.42
FYN P06241 1/20 0.42
BLM P54132 2/20 0.40
MEN1 O00255 1/20 0.40
LDHA P00338 1/20 0.40
KMT2A Q03164 1/20 0.40
HDAC3 O15379 1/20 0.39
HDAC1 Q13547 1/20 0.39
HDAC2 Q92769 1/20 0.39
HDAC8 Q9BY41 1/20 0.39
ALOX15 P16050 1/20 0.39
PMP22 Q01453 1/20 0.39
CASP1 P29466 1/20 0.38

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.

Compoundsimilaritytop predictedshared targets
Acetic Acid SCHEMBL1035225 1.00
Acetic Acid SCHEMBL8693841 0.95 CA1 (0.82) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL8012154 0.95 CA1 (1.00) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL153505 0.95 CA1 (1.00) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL1331799 0.95
Acetic Acid SCHEMBL10529780 0.95 CA1 (1.00) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL2343612 0.95 CA1 (1.00) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL1964006 0.95 CA1 (1.00) CA1CA4FAHD1LMNAFFAR3
Acetic Acid SCHEMBL2289 0.95
Acetic Acid SCHEMBL1332333 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

Claimed or disclosed in 314 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122079848-A Synthesis method of illite-kali plug 2026-05-26 CN claimed
CN-117362170-A Preparation method of cable Ma Lutai intermediate 四川美大康华康药业有限公司 2024-01-09 CN claimed
CN-114605366-B Synthesis method and synthesis system for preparing hydroxypropyl pyrantriol by continuous flow 拓信达(启东)医药生物科技有限公司 2023-10-10 CN claimed
CN-116444590-A Preparation method of aminoglycoside compound 无锡富泽药业有限公司 2023-07-18 CN claimed
CN-110596067-A Formaldehyde detection method 杭州柘大飞秒检测技术有限公司 2019-12-20 CN claimed
EP-2431368-B1 CNS active fused bicycloheterocycle substituted azabicyclic alkane derivatives ABBVIE BAHAMAS LTD (BS) 2014-08-27 EP claimed
CN-102741227-B Aryl benzylamine compounds NOVARTIS AG 2014-07-30 CN claimed
EP-2531487-B1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2014-06-18 EP claimed
EP-2531487-A1 ARYL BENZYLAMINE COMPOUNDS Novartis AG (CH) 2012-12-12 EP claimed
WO-2011095452-A1 ARYL BENZYLAMINE COMPOUNDS NOVARTIS AG (CH) 2011-08-11 WO claimed
CN-122079848-A Synthesis method of illite-kali plug 2026-05-26 CN disclosed
US-20260137803-A1 LIPID NANOPARTICLES AND METHODS OF MANUFACTURE AND USE THEREOF GENZYME CORP (US) 2026-05-21 US disclosed
EP-4741383-A1 COMPOUND AND USE THEREOF AS ANTI-CANCER DRUG Tyligand Bioscience (Shanghai) Limited (CN) 2026-05-13 EP disclosed
US-12583839-B2 PD-L1 antagonist compound ADLAI NORTYE BIOPHARMA CO., LTD. (CN) 2026-03-24 US disclosed
EP-4658313-A1 HSC-SPECIFIC ANTIBODY CONJUGATED LIPID NANOPARTICLES AND USES THEREOF GENZYME CORPORATION (US) 2025-12-10 EP disclosed
WO-2000047212-A1 QUINAZOLINE DERIVATIVES AS ANGIOGENESIS INHIBITORS ASTRAZENECA AB (SE) 2000-08-17 WO disclosed
EP-0999205-A1 AMINOCYCLOALKANE COMPOUNDS Mitsubishi-Tokyo Pharmaceuticals, Inc. (JP) 2000-05-10 EP disclosed
EP-0976753-A1 [1,2,4]TRIAZOLO[1,5-c]PYRIMIDINE DERIVATIVES KYOWA HAKKO KOGYO CO., LTD. (JP) 2000-02-02 EP disclosed
US-5972947-A ANTICOAGULANT, CARDIOVASCULAR DISORDERS, ANTIINFLAMMATORY AGENTS, OSTEOPOROSIS, ANTITUMOR AGENT ROCHE DIAGNOSTICS GMBH (DE) 1999-10-26 US disclosed
WO-1999045925-A1 NOVEL OPIATE COMPOUNDS, METHODS OF MAKING AND METHODS OF USE RESEARCH TRIANGLE INSTITUTE (US) 1999-09-16 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 (2 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-12583839-B2 PD-L1 antagonist compound CD274, PDCD1LG2, PDCD1 CA1 1594/4885CA4 2128/4885FAHD1 4389/4885
US-20260137803-A1 LIPID NANOPARTICLES AND METHODS OF MANUFACTURE AND USE THEREOF CD2BP2, CD2, CD4 CA1 1954/4885CA4 3117/4885FAHD1 3526/4885

“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.