Iodipamide Meglumine
This meglumine salt of iodipamide is an intravenous cholangiographic contrast medium used to visualize the biliary system on X-ray. After injection, it is excreted in bile, opacifying the bile ducts. Like other iodinated contrast agents, it carries a risk of allergic reactions and renal injury.
الوزن الجزيئي
1530,2000 g/mol
TPSA
359,00 Ų
آلية العمل
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.
البنية ثنائية الأبعاد
Cite this structure
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SMILES
CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.O=C(CCCCC(=O)Nc1c(I)cc(I)c(C(=O)O)c1I)Nc1c(I)cc(I)c(C(=O)O)c1I
InChI
InChI=1S/C20H14I6N2O6.2C7H17NO5/c21-7-5-9(23)17(15(25)13(7)19(31)32)27-11(29)3-1-2-4-12(30)28-18-10(24)6-8(22)14(16(18)26)20(33)34;2*1-8-2-4(10)6(12)7(13)5(11)3-9/h5-6H,1-4H2,(H,27,29)(H,28,30)(H,31,32)(H,33,34);2*4-13H,2-3H2,1H3/t;2*4-,5+,6+,7+/m.00/s1
Molecular Formula
C34H48I6N4O16
HBD / HBA
16 / 18
الروابط القابلة للدوران
21
الذرات الثقيلة
60
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.
الأسئلة الشائعة
This meglumine salt of iodipamide is an intravenous cholangiographic contrast medium used to visualize the biliary system on X-ray. After injection, it is excreted in bile, opacifying the bile ducts. Like other iodinated contrast agents, it carries a risk of allergic reactions and renal injury.
Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.
Yes, Iodipamide Meglumine 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). CHEMBL3989806. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 636408. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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