MAGNESIUM OXIDE


Synonyms	E-530 E530 Heavy magnesium oxide INS NO.530 INS-530 Light magnesium oxide Mag ox Mag-ox 400 Magdose Magnesia Magnesia oxydata Magnesii oxidum Magnesium (as oxide) Magnesium oxide Magnesium oxide heavy Magnesium oxide, heavy Magnesium oxide, light Magstar Oromag 160 Oximag Uro-mag
Status
Molecule Category	Free-form
ATC	A02AA02 A06AD02 A12CC10
UNII	3A3U0GI71G


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

Structure


InChI Key	CPLXHLVBOLITMK-UHFFFAOYSA-N
Smiles	O=[Mg]
InChI	InChI=1S/Mg.O

Physicochemical Descriptors

Property Name	Value
Molecular Formula	MgO
Molecular Weight	40.3
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	CHEMBL1200572
DrugCentral	4293
FDA SRS	3A3U0GI71G
Human Metabolome Database	HMDB0015458
PharmGKB	PA450298
PubChem	6850729
SureChEMBL	SCHEMBL728988

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).