Acetic Acid

Acetic Acid

SCHEMBL4634983

CC(=O)[O-].C[N+](CCO)(CCO)CCO

nearest known ligand 0.44

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
CHRNB4 known ✓ P30926 1/20 0.32
CHRNA3 known ✓ P32297 1/20 0.32
CA1 P00915 2/20 0.44
MEN1 O00255 1/20 0.41
LMNA P02545 1/20 0.41
KMT2A Q03164 1/20 0.41
CYP3A4 P08684 1/20 0.41
SLC5A7 Q9GZV3 1/20 0.41
BBOX1 O75936 6/20 0.38
GALR3 O60755 1/20 0.37
PSMD14 O00487 1/20 0.35
PLA2G1B P04054 1/20 0.35
MMP2 P08253 1/20 0.35
RAD52 P43351 1/20 0.35
ATG4B Q9Y4P1 1/20 0.35
ACHE P22303 1/20 0.33
CA4 P22748 1/20 0.33
PGR P06401 1/20 0.32
CHRM2 P08172 1/20 0.32
CHRM4 P08173 1/20 0.32

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
Bicarbonate SCHEMBL17888821 0.92 MEN1 (0.43) MEN1LMNAKMT2ACYP3A4SLC5A7
Acetic Acid SCHEMBL15826260 0.91 BBOX1 (0.42) CA1MEN1LMNAKMT2ACYP3A4
Bicarbonate SCHEMBL8995792 0.89 MEN1 (0.41) MEN1LMNAKMT2ACYP3A4SLC5A7
Bicarbonate SCHEMBL7574736 0.89 LMNA (0.41) MEN1LMNAKMT2ACYP3A4SLC5A7
Acetic Acid SCHEMBL15820391 0.89 BBOX1 (0.41) CA1MEN1LMNAKMT2ACYP3A4
Acetic Acid SCHEMBL15820741 0.87 BBOX1 (0.39) CA1MEN1LMNAKMT2ABBOX1
Acetic Acid SCHEMBL2920415 0.83 DNM1 (0.46) CA1MEN1LMNAKMT2ACYP3A4
Choline SCHEMBL316506 0.83 LMNA (0.63) CA1MEN1LMNAKMT2ACYP3A4
Acetic Acid SCHEMBL28437505 0.83 DNM1 (0.53) BBOX1PSMD14PLA2G1BMMP2RAD52
Acetic Acid SCHEMBL28670247 0.83 DNM1 (0.53) BBOX1PSMD14PLA2G1BMMP2RAD52

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 17 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120026412-A Mushroom fiber electrode and preparation method thereof 武汉纺织大学 2025-05-23 CN claimed
CN-119956526-A Mushroom fiber, green preparation method and application thereof 武汉纺织大学 2025-05-09 CN claimed
CN-120026412-A Mushroom fiber electrode and preparation method thereof 武汉纺织大学 2025-05-23 CN disclosed
CN-119956526-A Mushroom fiber, green preparation method and application thereof 武汉纺织大学 2025-05-09 CN disclosed
US-20150335547-A1 ORAL CARE COMPOSITION CONTAINING IONIC LIQUIDS COLGATE-PALMOLIVE COMPANY (US) 2015-11-26 US disclosed
EP-2934469-A2 ORAL CARE COMPOSITION CONTAINING IONIC LIQUIDS Colgate-Palmolive Company (US) 2015-10-28 EP disclosed
WO-2014098871-A2 ORAL CARE COMPOSITION CONTAINING IONIC LIQUIDS COLGATE-PALMOLIVE COMPANY (US) 2014-06-26 WO disclosed
EP-1663486-A4 LOW-ODOR CATALYST FOR ISOCYANATE-DERIVED FOAMS AND ELASTOMERS HUNTSMAN SPEC CHEM CORP (US) 2008-06-11 EP disclosed
US-20070282026-A1 Low-Odor Catalyst for Isocyanate-Derived Foams and Elastomers HUNTSMAN PETROCHEMICAL CORPORATION (US) 2007-12-06 US disclosed
EP-1663486-A2 LOW-ODOR CATALYST FOR ISOCYANATE-DERIVED FOAMS AND ELASTOMERS HUNTSMAN PETROCHEMICAL CORPORATION (US) 2006-06-07 EP disclosed
WO-2005009601-A2 LOW-ODOR CATALYST FOR ISOCYANATE-DERIVED FOAMS AND ELASTOMERS HUNTSMAN PETROCHEMICAL CORPORATION (US) 2005-02-03 WO disclosed
EP-0523483-B1 Process for the preparation of screen fractions of bead-form, expandable styrene polymers prepared by suspension polymerisation BASF AG (DE) 1995-12-06 EP disclosed
EP-0470455-B1 Antistatic expansible polystyrene pearls BASF AG (DE) 1995-09-27 EP disclosed
US-5286756-A With antistatic agent; metal-free coating BASF AKTIENGESELLSCHAFT (DE) 1994-02-15 US disclosed
EP-0523483-A1 Process for the preparation of screen fractions of bead-form, expandable styrene polymers prepared by suspension polymerisation BASF Aktiengesellschaft (DE) 1993-01-20 EP disclosed
US-5110835-A Coated with hydroxyl-containing quaternary ammonium salt BASF AKTIENGESELLSCHAFT (DE) 1992-05-05 US disclosed
EP-0470455-A2 Antistatic expansible polystyrene pearls BASF Aktiengesellschaft (DE) 1992-02-12 EP 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-20150335547-A1 ORAL CARE COMPOSITION CONTAINING IONIC LIQUIDS MCOLN3, TAS2R39, TAS2R40 CHRNB4 3065/4885CHRNA3 2311/4885CA1 1525/4885

“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.