Sodium Acetate

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Also known as Acetic acid, sodium salt (1:1)E-262(I)E262FEMA NO. 3024INS NO.262(I)INS-262(I)NSC-77459Sodium acetate (3h2o)Sodium acetate anhydrousSodium acetate component of procalamineSodium acetate hydrateSodium acetate trihydrateanhydrousSodium salt acetateSID144209939

Summary

Sodium Acetate (CHEMBL1354) is an approved small molecule (ATC B05XA08); indicated across 5 conditions including ornithine carbamoyltransferase deficiency and brain neoplasm.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: B05XA08
  • Indications: 5 conditions
  • Clinical trials: 1
  • Chemistry: 59.04 Da · C2H3O2-

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1354
NameSodium Acetate
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID175
ChEBICHEBI:32954
ATCB05XA08
Molecular formulaC2H3O2-
Molecular weight59.04
InChIKeyQTBSBXVTEAMEQO-UHFFFAOYSA-M

SMILES: CC(=O)[O-]

IUPAC name: acetate

Also known as: Acetic acid, sodium salt (1:1), E-262(I), E262, FEMA NO. 3024, INS NO.262(I), INS-262(I), NSC-77459, Sodium acetate, Sodium acetate (3h2o), Sodium acetate anhydrous, Sodium acetate component of procalamine, Sodium acetate hydrate

Parent form; salt/anhydrous children: CHEMBL2107054

Patent coverage: 221,447 distinct patent families (594,259 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Carbonic anhydrase 1, Carbonic anhydrase.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

5 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
ornithine carbamoyltransferase deficiency3MONDO:0010703EFO:0007409
brain neoplasm2MONDO:0021211EFO:0003833
stroke disorder2MONDO:0005098EFO:0000712

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 1.

Phase distribution

PhaseTrials
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05345171PHASE3ACTIVE_NOT_RECRUITINGClinical Study of DTX301 AAV-Mediated Gene Transfer for Ornithine Transcarbamylase (OTC) Deficiency

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).