Zinc Acetate Anhydrous

drug
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Also known as Acetic acid, zinc(ii) saltAnhydrous zinc acetateE650NSC-75801Zincum aceticumZinc acetateSID144212333

Summary

Zinc Acetate Anhydrous (CHEMBL1200928) is an approved small-molecule astringent; indicated across 5 conditions including pneumonia and wilson disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 5 conditions
  • Clinical trials: 12
  • Chemistry: 183.5 Da · C4H6O4Zn

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1200928
NameZinc Acetate Anhydrous
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID11192
ChEBICHEBI:62984
Molecular formulaC4H6O4Zn
Molecular weight183.5
InChIKeyDJWUNCQRNNEAKC-UHFFFAOYSA-L

SMILES: CC(=O)[O-].CC(=O)[O-].[Zn+2]

IUPAC name: zinc diacetate

ChEBI definition: An acetate salt in which the cationic component is zinc(2+).

Pharmacological roles (ChEBI): astringent.

Also known as: Acetic acid, zinc(ii) salt, Anhydrous zinc acetate, E650, NSC-75801, Zinc acetate anhydrous, Zincum aceticum, Zinc acetate, SID144212333, ZINC ACETATE ANHYDROUS

Parent form; salt/anhydrous children: CHEMBL3184986

Patent coverage: 44,972 distinct patent families (101,441 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 100,605 (99%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

No target linkage available.

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 (0 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
pneumonia3MONDO:0005249EFO:0003106
Wilson disease3MONDO:0010200MONDO:0010200
stomatitis2MONDO:0004842EFO:1001904
severe acute respiratory syndrome2MONDO:0005091MONDO:0100096

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

Clinical trials

Total trials: 12.

Phase distribution

PhaseTrials
Not specified5
PHASE42
PHASE32
PHASE2/PHASE31
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00004338PHASE4COMPLETEDStudy of Zinc for Wilson Disease
NCT05778383PHASE4COMPLETEDZinc Supplementation Impact in Acute COVID-19 Clinical Outcomes
NCT00212368PHASE3COMPLETEDEfficacy and Safety Study of Zinc Acetate to Treat Wilson’s Disease in Japan.
NCT00373100PHASE3COMPLETEDThe Efficacy of Zinc as Adjunct Therapy in the Treatment of Severe Pneumonia in Children
NCT02868151PHASE2/PHASE3COMPLETEDEffect of Oral Vitamin C in Assessing the Severity of Oral Mucositis in Chemoradiation of Head and Neck Cancers
NCT04621149PHASE2TERMINATEDAn Outpatient Study Investigating Non-prescription Treatments for COVID-19
NCT00696410PHASE1COMPLETEDThe Impact of Zinc Supplementation on Left Ventricular Function in Nonischemic Cardiomyopathy
NCT06612554Not specifiedRECRUITINGZn Supplementation in HIV Immunological Non Responders
NCT00981448Not specifiedCOMPLETEDNutrigenomics of Zinc Supplementation in Insulin Secretion and Diabetes
NCT03532555Not specifiedTERMINATEDEnteral Zinc to Improve Growth in Infants at Risk for Bronchopulmonary Dysplasia
NCT04828538Not specifiedWITHDRAWNVitamin D, Omega-3, and Combination Vitamins B, C and Zinc Supplementation for the Treatment and Prevention of COVID-19
NCT05095493Not specifiedCOMPLETEDOral Zinc Supplementation to Enhance Botulinum Neurotoxin Response

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 1 clinical and 1 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

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