DIATRIZOATE MEGLUMINE


Trade Names	ANGIOVIST 282 CARDIOGRAFIN CYSTOGRAFIN CYSTOGRAFIN DILUTE DIATRIZOATE MEGLUMINE HYPAQUE HYPAQUE-CYSTO RENO-30 RENO-60 RENO-DIP UROVIST CYSTO UROVIST CYSTO PEDIATRIC UROVIST MEGLUMINE DIU/CT
Synonyms	Angiovist 282 Cardiografin Cystografin Cystografin dilute Diatrizoate meglumine Diatrizoate methylglucamine Diatrizoic acid meglumine salt Hypaque Hypaque-cysto Meglumine amidotrizoate Meglumine amidotrizoate injection Meglumine diatrizoate Reno Reno-30 Reno-60 Reno-dip Urovist cysto Urovist cysto pediatric Urovist meglumine diu/ct
Status
Molecule Category	Mixture
UNII	3X9MR4N98U
EPA CompTox	DTXSID20897171


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

Structure


InChI Key	MIKKOBKEXMRYFQ-WZTVWXICSA-N
Smiles	CC(=O)Nc1c(I)c(NC(C)=O)c(I)c(C(=O)O)c1I.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
InChI	InChI=1S/C11H9I3N2O4.C7H17NO5/c1-3(17)15-9-6(12)5(11(19)20)7(13)10(8(9)14)16-4(2)18;1-8-2-4(10)6(12)7(13)5(11)3-9/h1-2H3,(H,15,17)(H,16,18)(H,19,20);4-13H,2-3H2,1H3/t;4-,5+,6+,7+/m.0/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C18H26I3N3O9
Molecular Weight	809.13
AlogP	3.12
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	3.0
Polar Surface Area	95.5
Molecular species	ACID
Aromatic Rings	1.0
Heavy Atoms	20.0

Bioactivity

Mechanism of Action	Action	Reference
Diagnostic agent	None	DailyMed

Cross References

Resources	Reference
ChEBI	31812
ChEMBL	CHEMBL1200839
FDA SRS	3X9MR4N98U
PubChem	8566
SureChEMBL	SCHEMBL107036

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).