Acetic Acid

Acetic Acid

SCHEMBL983612

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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 SCHEMBL196205 1.00
Acetic Acid SCHEMBL1168762 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL28703302 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL27279038 0.91 CA1 (0.73) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL3711688 0.91
Acetic Acid SCHEMBL1168096 0.91 CA1 (0.73) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL9117998 0.89 CA1 (0.89) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL140294 0.89
Acetic Acid SCHEMBL119187 0.89 CA1 (0.89) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL135062 0.89 CA1 (0.89) 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

Claimed or disclosed in 366 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260036897-A1 REPAIR PROCESS FOR CLEAR DEFECTS ON EUV PSM MASKS ZEISS CARL SMT GMBH (DE) 2026-02-05 US claimed
WO-2025061949-A2 METHOD AND DEVICE FOR MASK REPAIR CARL ZEISS SMT GMBH (DE) 2025-03-27 WO claimed
CN-119215982-A Catalyst for co-production of dimethyl carbonate and monomethyl malonate, and preparation method and application thereof 中国石油化工股份有限公司 2024-12-31 CN claimed
WO-2024223530-A1 REPAIR PROCESS FOR CLEAR DEFECTS ON EUV PSM MASKS CARL ZEISS SMT GMBH (DE) 2024-10-31 WO claimed
EP-3195932-B1 HYDROSILYLATION REACTION CATALYST UNIV KYUSHU NAT UNIV CORP (JP) 2024-08-21 EP claimed
CN-116514621-B Method for constructing C-C bond at ortho-position of aryl by metal-catalyzed sulfur ylide and aryl sulfur/selenoacetic acid ester rearrangement reaction 四川大学 2024-04-09 CN claimed
CN-117679340-A Anti-aging composition containing epidermal growth factor and preparation method and application thereof 湖南湘妃医疗器械有限公司 2024-03-12 CN claimed
CN-117164497-A Synthesis method of pyrrole-2-ketone compound 华南理工大学 2023-12-05 CN claimed
CN-113443970-B Synthesis method of 4-alkoxy phenol compound 新乡医学院 2023-04-07 CN claimed
CN-110483272-B Novel method for asymmetric synthesis of (1S,2S) -2-fluorocyclopropanecarboxylic acid by catalysis of chiral rhodium catalyst 广州康瑞泰药业有限公司 2022-09-27 CN claimed
CN-109400629-B Indole spirooxazine heterocyclic compound and preparation method thereof 江西师范大学 2022-07-12 CN claimed
CN-114433239-A Rhodium nanoparticle dispersion and preparation method and application thereof 中国石油化工股份有限公司 2022-05-06 CN claimed
CN-113582993-B Condensed polycyclic compound containing triazahydronaphthalene structure and preparation method and application thereof 广州大学 2022-04-19 CN claimed
EP-4748840-A1 IMIDAZO[1,2-A]PYRIDINE TYPE IRAK DEGRADATION AGENT AND USE THEREOF TAINUORUI (TIANJIN) BIOTECHNOLOGY CO., LTD (CN) 2026-05-27 EP disclosed
EP-4747253-A1 SPIROCYCLIC WRN HELICASE INHIBITORS Merck Sharp & Dohme LLC (US) 2026-05-27 EP disclosed
CN-116768861-B SOS1 protein degradation targeting chimeric and composition, preparation and application thereof 北京福元医药股份有限公司 2026-05-12 CN disclosed
WO-2000059854-A1 METHOD FOR PRODUCING ALKAPOLYENYL COMPOUNDS USING CERTAIN COCATALYSTS BASF AKTIENGESELLSCHAFT (DE) 2000-10-12 WO disclosed
WO-2000018759-A1 PHENYLALANINE DERIVATIVES AS ALPHA 4 INTEGRIN INHIBITORS CELLTECH THERAPEUTICS LIMITED (GB) 2000-04-06 WO disclosed
WO-1995016686-A1 HETEROARYL MUPIROCIN DERIVATIVES USEFUL AS ANTIBACTERIAL, ANTIFUNGAL OR HERBICIDAL AGENTS SMITHKLINE BEECHAM PLC (GB) 1995-06-22 WO disclosed
US-4535169-A 5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano[2,3-b]pyrrole and the preparation thereof THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 1985-08-13 US 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20260036897-A1 REPAIR PROCESS FOR CLEAR DEFECTS ON EUV PSM MASKS PML, MUS81, PSMD14 CA1 3642/4885CA4 2440/4885LMNA 584/4885

“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.