ZINC ACETATE


Trade Names	GALZIN
Synonyms	E650 Galzin NPC-02 NSC-75801 Npc-02 Wilzin Zinc acetate Zinc acetate dihydrate Zinc acetate hydrate Zinci acetas
Status
Molecule Category	Salt-form
ATC	A16AX05
UNII	FM5526K07A
EPA CompTox	DTXSID5021461
Parent Compound:


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	BEAZKUGSCHFXIQ-UHFFFAOYSA-L
Smiles	CC(=O)[O-].CC(=O)[O-].O.O.[Zn+2]
InChI	InChI=1S/2C2H4O2.2H2O.Zn/c21-2(3)4;;;/h21H3,(H,3,4);2*1H2;/q;;;;+2/p-2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C4H6O4Zn
Molecular Weight	183.48
AlogP	None
Hydrogen Bond Acceptor	None
Hydrogen Bond Donor	None
Number of Rotational Bond	None
Polar Surface Area	None
Molecular species	None
Aromatic Rings	None
Heavy Atoms	None

Cross References

Resources	Reference
ChEMBL	CHEMBL3184986
FDA SRS	FM5526K07A
PubChem	2724192
SureChEMBL	SCHEMBL94413
ChEBI	62984
ChEMBL	CHEMBL1200928
DrugBank	DB14487
FDA SRS	H2ZEY72PME
PubChem	2724192
SureChEMBL	SCHEMBL51

CONTENTS


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).