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Iomeprol
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Iomeprol
Clinical data
Trade namesIomervu, others
License data
Routes of
administration
Intravenous, intra-arterial
ATC code
Legal status
Legal status
Pharmacokinetic data
Metabolismnone
Elimination half-life109±20 min
ExcretionKidney
Identifiers
  • 1-N,3-N-bis(2,3-dihydroxypropyl)-5-(2-hydroxy-N-methylacetamido)-2,4,6-triiodobenzene-1,3-dicarboxamide
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H22I3N3O8
Molar mass777.089 g·mol−1
3D model (JSmol)
  • Ic1c(c(I)c(c(I)c1N(C(=O)CO)C)C(=O)NCC(O)CO)C(=O)NCC(O)CO
  • InChI=1S/C17H22I3N3O8/c1-23(9(29)6-26)15-13(19)10(16(30)21-2-7(27)4-24)12(18)11(14(15)20)17(31)22-3-8(28)5-25/h7-8,24-28H,2-6H2,1H3,(H,21,30)(H,22,31)
  • Key:NJKDOADNQSYQEV-UHFFFAOYSA-N

Iomeprol, sold under the brand name Imeron among others, is a medication used as a radiocontrast agent in X-ray imaging.[1][2][3]

Iomeprol was approved for medical use in the United States in November 2024.[1][4][5]

Side effects

[edit]

It is classified as a water-soluble, nephrotrophic, low osmolar X-ray contrast medium.[2] Low osmolar non-ionic agents are better tolerated and less likely to cause side effects than the high osmolar ionic agents.[2]

Society and culture

[edit]

Iomeprol is not metabolized in the human body but excreted in unchanged form.[medical citation needed] It is decomposed slowly and can therefore accumulate in the environment.[6]

[edit]

Iomeprol was approved for medical use in the United States in November 2024.[1][4]

Brand names

[edit]

Iomeprol is sold under the brand name Iomervu.[1]

References

[edit]
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