Acetic Acid

Acetic Acid

SCHEMBL135063

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Ru+4]

nearest known ligand 0.89

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 18)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.89
CA4 P22748 3/20 0.58
LMNA P02545 2/20 0.50
TSHR P16473 2/20 0.46
THPO P40225 1/20 0.46
FFAR3 O14843 1/20 0.46
LCK P06239 1/20 0.46
FYN P06241 1/20 0.46
ALOX15 P16050 1/20 0.42
BLM P54132 1/20 0.42
PMP22 Q01453 1/20 0.42
FAHD1 Q6P587 1/20 0.42
ALDH1A1 P00352 4/20 0.36
TDP1 Q9NUW8 1/20 0.36
KDM4E B2RXH2 1/20 0.36
CA2 P00918 1/20 0.36
PTGS1 P23219 1/20 0.36
MMP12 P39900 1/20 0.36

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 SCHEMBL175976 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL10578734 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL28222794 0.95
Acetic Acid SCHEMBL4398779 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL1405526 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL28441649 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL29827217 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL1367766 0.95
Acetic Acid SCHEMBL28305774 0.95
Acetic Acid SCHEMBL11699358 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO

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 3455 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122082022-A Trimetallic iridium-based anode catalyst, preparation method and application thereof 2026-05-26 CN claimed
CN-122091617-A Molybdenum ruthenium oxide loaded Pt anti-counter electrode catalyst for fuel cell anode and preparation method thereof 2026-05-26 CN claimed
CN-122077008-A Preparation method and application of graphene-supported iridium-ruthenium-cobalt-copper-nickel high-entropy nanoparticles 2026-05-26 CN claimed
CN-122057550-A Ultralow-load Ru-based monoatomic catalyst, preparation and application thereof in propylene preparation by propane dehydrogenation 中国科学院大连化学物理研究所 2026-05-19 CN claimed
CN-122032639-A Preparation method of bisphenol A hydrogenation catalyst and bisphenol A hydrogenation catalyst 中国石油天然气股份有限公司 2026-05-15 CN claimed
CN-122032648-A Liquid phase catalyst for hydrochlorination of acetylene and application thereof 天津大学 2026-05-15 CN claimed
CN-122039147-A Ternary Ru-based solid solution high-oxidizing-power electrocatalyst for long-term stable electrolysis of water to produce oxygen, and preparation method and application thereof 中国人民大学 2026-05-15 CN claimed
CN-118047698-B Preparation method of N- [ (1R) -2- [1,1' -biphenyl ] -4-yl-1- (hydroxymethyl) ethyl ] carbamic acid tert-butyl ester 山东科巢生物制药有限公司 2026-05-12 CN claimed
CN-122013243-A Doped ruthenium-based catalyst, and preparation method and application thereof 景德镇陶瓷大学 2026-05-12 CN claimed
CN-122006779-A Composite catalyst for preparing furan by using furfural and preparation method thereof 陕西蒲城万德科技有限公司 2026-05-12 CN claimed
US-4332915-A CATALYST SYSTEM COMPRISING RUTHENIUM COMPOUND AND COBALT COMPOUND DISPERSED IN LOW MELTING QUATERNARY PHOSPHONIUM OR AMMONIUM BASE OR SALT TEXACO INC. (US) 1982-06-01 US claimed
US-4332914-A A CATALYST SYSTEM COMPRISING A RUTHENIUM AND RHENIUM OR MANGANESE CONTAINING COMPOUND TEXACO INC. (US) 1982-06-01 US claimed
US-4270015-A CATALYTIC ESTERIFICATION OF AN ACYCLIC ACID USING A COMPLEX OF A RUTHENIUM COMPOUND AND A CESIUM, QUATERNARY AMMONIUM, OR PHOSPHONIUM COMPOUND; PYROLYSIS TEXACO INC. (US) 1981-05-26 US claimed
US-4268689-A ALIPHATIC CARBOXYLIC ACID, RUTHENIUM OR OSMIUM CATALYST, SALT COCATALYST TEXACO DEVELOPMENT CORP. (US) 1981-05-19 US claimed
US-4265828-A RUTHENIUM CATALYST WITH A LOW MELTING QUATERNARY PHOSPHONIUM OR AMMONIUM SALT TEXACO DEVELOPMENT CORP. (US) 1981-05-05 US claimed
US-4260820-A HOMOLOGATION WITH SYNTHESIS GAS USING IODIDE OR BROMIDE PROMOTER WITH RUTHENIUM COMPOUND CATALYST TEXACO DEVELOPMENT CORP. (US) 1981-04-07 US claimed
US-4239924-A COBALT CARBONYL COMPLEX ALKYLATION CATALYST, IODINE COMPOUND PROMOTER, HIGHLY SELECTIVE GULF RESEARCH & DEVELOPMENT COMPANY (US) 1980-12-16 US claimed
EP-0013464-A1 Selective formation of ethanol from methanol, hydrogen and carbon monoxide GULF RESEARCH & DEVELOPMENT COMPANY (US) 1980-07-23 EP claimed
US-4144399-A OSMIUM OR RUTHENIUM-CONTAINING CATALYST ATLANTIC RICHFIELD COMPANY (US) 1979-03-13 US claimed
US-4133966-A SELECTIVE CATALYST SYSTEM OF COBALT ACETYLACETONATE, GROUP VA ORGAN/COMPOUND, IODINE PROMOTER AND RUTHENIUM COMPOUND PROMOTER GULF RESEARCH & DEVELOPMENT COMPANY (US) 1979-01-09 US claimed