Iomeprol
This nonionic iodinated contrast agent is injected into blood vessels or body cavities to enhance visibility on CT scans and other X-ray procedures. It is considered safer than older ionic contrast agents because it causes fewer adverse reactions.
Molecular Weight
777.1000 g/mol
LogP
-2.30
TPSA
180.00 Ų
Lipinski RO5
Fail
Therapeutic Areas
Mechanism of Action
Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.
2D Structure
Cite this structure
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SMILES
CN(C(=O)CO)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
InChI
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)
Molecular Formula
C17H22I3N3O8
HBD / HBA
7 / 8
Rotatable Bonds
10
Heavy Atoms
31
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Frequently Asked Questions
This nonionic iodinated contrast agent is injected into blood vessels or body cavities to enhance visibility on CT scans and other X-ray procedures. It is considered safer than older ionic contrast agents because it causes fewer adverse reactions.
Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.
Yes, Iomeprol is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2107214. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3731. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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