Ioversol

Ioversol
Clinical data
Trade names	Optiray
AHFS/Drugs.com	Micromedex Detailed Consumer Information
Pregnancy; category	AU: B1;
ATC code	V08AB07 (WHO) ;
Legal status
Legal status	AU: Unscheduled ;
Identifiers
	IUPAC name 1-N,3-N-bis(2,3-dihydroxypropyl)-5-[2-hydroxy-N-(2-hydroxyethyl)acetamido]-2,4,6-triiodobenzene-1,3-dicarboxamide;
CAS Number	87771-40-2 ;
PubChem CID	3741;
ChemSpider	3610 ;
UNII	N3RIB7X24K;
KEGG	D01555 ;
ChEMBL	ChEMBL1200614 ;
CompTox Dashboard (EPA)	DTXSID2045521 ;
ECHA InfoCard	100.118.911
Chemical and physical data
Formula	C18H24I3N3O9
Molar mass	807.115 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C(CO)N(C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)C(=O)NCC(CO)O)I)C(=O)CO;
	InChI InChI=1S/C18H24I3N3O9/c19-13-11(17(32)22-3-8(29)5-26)14(20)16(24(1-2-25)10(31)7-28)15(21)12(13)18(33)23-4-9(30)6-27/h8-9,25-30H,1-7H2,(H,22,32)(H,23,33) ; Key:AMDBBAQNWSUWGN-UHFFFAOYSA-N ;
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Ioversol (INN) is an organoiodine compound that is used as a contrast medium. It features both a high iodine content, as well as several hydrophilic groups. It is used in clinical diagnostics including arthrography, angiocardiography and urography.[1][2][3]

References

"Drug Information Portal - U.S. National Library of Medicine - Quick Access to Quality Drug Information". druginfo.nlm.nih.gov. Retrieved 9 January 2021.
"Optiray (ioversol) dosing, indications, interactions, adverse effects, and more". reference.medscape.com. Retrieved 9 January 2021.
Chen Y, Huang X, Huang S, Matchett M. "13. Fast-in-process method for the determination ioversol and related polar compounds by hydrophilic interactive chromatography". In Wang PG, He W (eds.). Hydrophilic Interaction Liquid Chromatography (HILIC) and Advanced Applications. CRC Press. p. 295-30. ISBN 978-1-4398-0753-8.

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