Acetic Acid

Acetic Acid

SCHEMBL170537

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Sn+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 SCHEMBL29157117 1.00 CA1 (0.89) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL8087817 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL30984409 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL15058608 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL9154222 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL9807643 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL9418227 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL9418238 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL4238250 0.95 CA1 (0.80) CA1CA4LMNATSHRTHPO
Acetic Acid SCHEMBL30984411 0.91 CA1 (0.73) 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 2604 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122035808-A Layered tin pyrophosphate composite anode material and preparation method thereof 辽宁石油化工大学 2026-05-15 CN claimed
CN-119241743-B Efficient and stable heterogeneous catalyst containing Lewis acid and preparation method and application thereof 沈阳化工大学 2026-05-15 CN claimed
CN-122039125-A Wood-derived carbon self-supporting transition metal core-shell hydrogen evolution catalyst and preparation method thereof 广西大学 2026-05-15 CN claimed
US-20260090178-A1 METHOD FOR PREPARING MID-INFRARED FOCAL PLANE DETECTOR BASED ON Sn-DOPED PbSe QUANTUM DOTS SUN YAT-SEN UNIVERSITY (CN) 2026-03-26 US claimed
US-20260082764-A1 OPTOELECTRONIC DEVICE AND PREPARATION METHOD THEREOF, AND DISPLAY DEVICE GUANGDONG JUHUA RESEARCH INSTITUTE OF ADVANCED DISPLAY (CN) 2026-03-19 US claimed
EP-4015592-B1 CURABLE CONDENSATION COMPOUNDS ON THE BASIS OF ALKOXY-FUNCTIONAL POLYSILOXANES EVONIK OPERATIONS GMBH (DE) 2026-03-18 EP claimed
EP-4688678-A1 COATED CONTAINER AND PROCESS OF PREPARATION Pilkington Group Limited (GB) 2026-02-11 EP claimed
US-12515964-B2 Tin oxide forming composition LG CHEM, LTD. (KR) 2026-01-06 US claimed
US-20260001858-A1 DEVICE SYSTEM AND METHOD FOR PREPARING CYCLIC CARBONATE BY DIOL ESTERIFYING CYCLIZATION HUIZHOU INSTITUTE OF GREEN ENERGY AND ADVANCED MAT (CN) 2026-01-01 US claimed
US-12460081-B2 Curable condensation compounds based on alkoxy-functional polysiloxanes EVONIK OPERATIONS GMBH (DE) 2025-11-04 US claimed
EP-0458877-A1 CALCIFICATION MITIGATION OF BIOPROSTHETIC IMPLANTS. BAXTER INT (US) 1991-12-04 EP claimed
EP-0444476-A2 Process for the preparation of tetraalkyltin Th. Goldschmidt AG (DE) 1991-09-04 EP claimed
US-5002566-A Impregnation of biological material with a calcification resistant material, adding ferric or stannic ion to biological material BAXTER INTERNATIONAL INC. (US) 1991-03-26 US claimed
US-4960466-A FORMING CADMIUM STANNATE IN PRESENCE OF BETA-DIKETONE AND NITROGEN COMPOUND, SUCH AS AMINE OR AMMONIA; HIGH ELECTRO-CONDUCTIVITY VICTORIAN SOLAR ENERGY COUNCIL (AU) 1990-10-02 US claimed
WO-1990009102-A1 CALCIFICATION MITIGATION OF BIOPROSTHETIC IMPLANTS BAXTER INTERNATIONAL INC. (US) 1990-08-23 WO claimed
EP-0286654-A4 COATING SOLUTIONS. VICTORIAN SOLAR ENERGY COUNCIL (AU) 1989-01-26 EP claimed
EP-0286654-A1 COATING SOLUTIONS Renewable Energy Authority Victoria (AU) 1988-10-19 EP claimed
WO-1988001988-A1 COATING SOLUTIONS VICTORIAN SOLAR ENERGY COUNCIL (AU) 1988-03-24 WO claimed
EP-0115176-B1 STANNIC N-PHOSPHONOMETHYLGLYCINE COMPOUNDS AND THEIR USE AS HERBICIDES STAUFFER CHEMICAL COMPANY (US) 1986-08-06 EP claimed
EP-0115176-A1 Stannic N-phosphonomethylglycine compounds and their use as herbicides STAUFFER CHEMICAL COMPANY (US) 1984-08-08 EP claimed