Zinc Acetate Anhydrous
Zinc acetate anhydrous is the non-hydrated form of zinc acetate, used for the same therapeutic indications including Wilson's disease management (blocking intestinal copper absorption through metallothionein induction) and zinc deficiency supplementation. The anhydrous form may have different solubility and bioavailability characteristics compared to the hydrated form but provides equivalent zinc supplementation and copper-blocking activity. It is also studied for cardiometabolic effects of zinc in conditions such as heart failure.
Moleküler Ağırlık
183,5000 g/mol
TPSA
80,30 Ų
Terapötik Alanlar
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D Yapı
Cite this structure
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SMILES
CC(=O)[O-].CC(=O)[O-].[Zn+2]
InChI
InChI=1S/2C2H4O2.Zn/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2
Molecular Formula
C4H6O4Zn
HBD / HBA
- / 4
Döndürülebilir Bağlar
0
Ağır Atomlar
9
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Sıkça Sorulan Sorular
Zinc acetate anhydrous is the non-hydrated form of zinc acetate, used for the same therapeutic indications including Wilson's disease management (blocking intestinal copper absorption through metallothionein induction) and zinc deficiency supplementation. The anhydrous form may have different solubility and bioavailability characteristics compared to the hydrated form but provides equivalent zinc supplementation and copper-blocking activity. It is also studied for cardiometabolic effects of zinc in conditions such as heart failure.
Yes, Zinc Acetate Anhydrous is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200928. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11192. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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