Iotrolan
This nonionic water-soluble iodinated contrast agent was developed specifically for imaging the fluid spaces around the brain and spinal cord (myelography and cisternography). Its water solubility allows it to mix with cerebrospinal fluid and be safely absorbed, unlike older oily contrast agents.
分子量
1626.2000 g/mol
LogP
-4.20
TPSA
400.00 Ų
リピンスキーの五則
不適合
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)
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
Cite this structure
Embed this structure
SMILES
CN(C(=O)CC(=O)N(C)c1c(I)c(C(=O)NC(CO)C(O)CO)c(I)c(C(=O)NC(CO)C(O)CO)c1I)c1c(I)c(C(=O)NC(CO)C(O)CO)c(I)c(C(=O)NC(CO)C(O)CO)c1I
InChI
InChI=1S/C37H48I6N6O18/c1-48(32-28(40)22(34(64)44-12(4-50)16(58)8-54)26(38)23(29(32)41)35(65)45-13(5-51)17(59)9-55)20(62)3-21(63)49(2)33-30(42)24(36(66)46-14(6-52)18(60)10-56)27(39)25(31(33)43)37(67)47-15(7-53)19(61)11-57/h12-19,50-61H,3-11H2,1-2H3,(H,44,64)(H,45,65)(H,46,66)(H,47,67)
Molecular Formula
C37H48I6N6O18
HBD / HBA
16 / 18
回転可能結合数
24
重原子数
67
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 water-soluble iodinated contrast agent was developed specifically for imaging the fluid spaces around the brain and spinal cord (myelography and cisternography). Its water solubility allows it to mix with cerebrospinal fluid and be safely absorbed, unlike older oily contrast agents.
Enhances the contrast of specific tissues or structures during medical imaging procedures by altering the local signal intensity or X-ray absorption characteristics.
Yes, Iotrolan is an approved drug. It has reached clinical phase 4. It is classified as a Unknown.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200555. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 3738. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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