Iomeprol

CHEMBL2107214 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
777.1 g/mol
LogP
-2.3
Phase
4

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.

分子量

777.1000 g/mol

LogP

-2.30

TPSA

180.00 Ų

リピンスキーの五則

不適合

治療領域

作用機序

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)

機序

Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.

2D構造

SVG PNG

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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

回転可能結合数

10

重原子数

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.

よくある質問

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 section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

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.

医学的免責事項

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.