English
Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C26H26I6N2O10
- Molecular weight
- 1287.9 g/mol
- IUPAC name
- 3-[3-[2-[2-[2-[3-(3-carboxy-2,4,6-triiodoanilino)-3-oxopropoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-2,4,6-triiodobenzoic acid
- SMILES
- C1=C(C(=C(C(=C1I)NC(=O)CCOCCOCCOCCOCCC(=O)NC2=C(C=C(C(=C2I)C(=O)O)I)I)I)C(=O)O)I
- InChIKey
- WWVAPFRKZMUPHZ-UHFFFAOYSA-N
- XLogP
- 4.2
- Polar surface area
- 170 Ų
- H-bond donors
- 4
- H-bond acceptors
- 10
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1982
- Admin. routes
- parenteral
via ChEMBL · EBI
Research
49 papers- Biotransformation of ioglycamic acid, iodoxamic acid and iotroxic acid in man.Investigative radiology · 1976
- Pharmacokinetics of iodoxamic acid in rhesus monkey: biliary excretion, plasma protein binding, and enterophepatic circulation.Journal of pharmaceutical sciences · 1978
- Kinetics of drug-drug interactions: biliary excretion of iodoxamic acid and iopanoic acid in rhesus monkeys.Journal of pharmaceutical sciences · 1979
- Gastrointestinal radiology. Pharmacokinetics of iopanoate and iodoxamate in rhesus monkeys.Investigative radiology · 1980
- [Pharmacology of iotroxic acid, a new intravenous cholangiographic agent. II. Experimental animal study of side effects].Arzneimittel-Forschung · 1978
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 1287.586
Show 3 more facts
- chemical formula
- C₂₆H₂₆I₆N₂O₁₀
- canonical SMILES
- C1=C(C(=C(C(=C1I)NC(=O)CCOCCOCCOCCOCCC(=O)NC2=C(C=C(C(=C2I)C(=O)O)I)I)I)C(=O)O)I
- subject has role
- contrast agent
Sources (2)
via Wikidata · CC0