Acetic Acid

Acetic Acid

SCHEMBL2944150

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].O.[Er+3]

nearest known ligand 0.80

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 0.80
CA4 P22748 3/20 0.54
LMNA P02545 2/20 0.46
ALDH1A1 P00352 3/20 0.43
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
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.

Compoundsimilaritytop predictedshared targets
Acetic Acid SCHEMBL94541 1.00 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL28776496 1.00 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL15618797 1.00 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL1026309 0.95 CA1 (0.89) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL23116337 0.90 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL25215531 0.90 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL21752870 0.90
Acetic Acid SCHEMBL25334487 0.90 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL21752953 0.90 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR
Acetic Acid SCHEMBL21752943 0.90 CA1 (0.80) CA1CA4LMNAALDH1A1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119816161-A Polarization micro LED device capable of adjusting luminous color and preparation method thereof 山东大学 2025-04-11 CN claimed
CN-117926221-A Device for forming corrosion-resistant coating and method for forming corrosion-resistant coating 中微半导体设备(上海)股份有限公司 2024-04-26 CN claimed
US-20240059620-A1 DENTAL CERAMIC COLORING SOLUTION KURARAY NORITAKE DENTAL INC. (JP) 2024-02-22 US claimed
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-111604086-B Preparation method and application of platinum-based normal paraffin aromatization catalyst 山东省科学院能源研究所 2024-01-19 CN claimed
EP-4223271-A1 DENTAL CERAMIC COLORING SOLUTION Kuraray Noritake Dental Inc. (JP) 2023-08-09 EP claimed
CN-116261436-A Ceramic coloring solution for dentistry 可乐丽则武齿科株式会社 2023-06-13 CN claimed
CN-115073815-B Environment-friendly heat stabilizer and preparation method thereof 山东浩纳新材料科技集团有限公司 2022-11-18 CN claimed
CN-115073815-A Environment-friendly heat stabilizer and preparation method thereof 山东浩纳新材料科技集团有限公司 2022-09-20 CN claimed
WO-2022071595-A1 DENTAL CERAMIC COLORING SOLUTION クラレノリタケデンタル株式会社 2022-04-07 WO claimed
CN-111604086-A Preparation method and application of platinum-based normal paraffin aromatization catalyst 山东省科学院能源研究所 2020-09-01 CN claimed
EP-2655482-A1 POLYHETEROSILOXANE COMPOSITION INCLUDING LANTHANIDE METAL Dow Corning Corporation (US) 2013-10-30 EP claimed
WO-2012088439-A1 POLYHETEROSILOXANE COMPOSITION INCLUDING LANTHANIDE METAL DOW CORNING CORPORATION (US) 2012-06-28 WO claimed
EP-1588423-A2 RARE EARTH DOPED GROUP IV NANOCRYSTAL LAYERS Group IV Semiconductor Inc. (CA) 2005-10-26 EP claimed
US-20040149353-A1 Doped semiconductor powder and preparation thereof KIRSTEEN MGMT. GROUP LLC 2004-08-05 US claimed
WO-2004066346-A2 RARE EARTH DOPED GROUP IV NANOCRYSTAL LAYERS GROUP IV SEMICONDUCTOR INC. (CA) 2004-08-05 WO claimed
CN-120899987-A Preparation method and application of piezoelectric material hydrogel for wound healing 哈尔滨工业大学(深圳)(哈尔滨工业大学深圳科技创新研究院) 2025-11-07 CN disclosed
CN-119976942-A Multicomponent rare earth oxide material with perovskite structure and preparation method thereof 天津大学 2025-05-13 CN disclosed
EP-1153005-A1 COMPOSITIONS COMPRISING NICKEL AND THEIR USE AS CATALYST IN OXIDATIVE DEHYDROGENATION OF ALKANES SYMYX TECHNOLOGIES (US) 2001-11-14 EP disclosed
WO-2000048971-A1 COMPOSITIONS COMPRISING NICKEL AND THEIR USE AS CATALYST IN OXIDATIVE DEHYDROGENATION OF ALKANES SYMYX TECHNOLOGIES, INC. (US) 2000-08-24 WO disclosed