Iohexol

drug
On this page

Also known as ExypaqueIohexolumNSC-759636OmnipaqueOmnipaque 12Omnipaque 140Omnipaque 180Omnipaque 210Omnipaque 240Omnipaque 300Omnipaque 350Omnipaque 70Omnipaque 9OraltagWIN 39424WIN-39424SID56322616SID29217758SID170464962

Summary

Iohexol (CHEMBL1200455) is an approved small-molecule radioopaque medium (ATC V08AB02); indicated across 9 conditions including myocardial ischemia and acute kidney injury.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: V08AB02
  • Indications: 9 conditions
  • Clinical trials: 62
  • Chemistry: 821.1 Da · C19H26I3N3O9

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1200455
NameIohexol
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID3730
ChEBICHEBI:31709
ATCV08AB02
Molecular formulaC19H26I3N3O9
Molecular weight821.1
InChIKeyNTHXOOBQLCIOLC-UHFFFAOYSA-N

SMILES: CC(=O)N(CC(CO)O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)C(=O)NCC(CO)O)I

IUPAC name: 5-[acetyl(2,3-dihydroxypropyl)amino]-1-N,3-N-bis(2,3-dihydroxypropyl)-2,4,6-triiodobenzene-1,3-dicarboxamide

ChEBI definition: A benzenedicarboxamide compound having N-(2,3-dihydroxypropyl)carbamoyl groups at the 1- and 3-positions, iodo substituents at the 2-, 4- and 6-positions and an N-(2,3-dihydroxypropyl)acetamido group at the 5-position.

Pharmacological roles (ChEBI): radioopaque medium.

Other ChEBI roles (chemical / environmental): environmental contaminant, xenobiotic.

Also known as: Exypaque, Iohexol, Iohexolum, NSC-759636, Omnipaque, Omnipaque 12, Omnipaque 140, Omnipaque 180, Omnipaque 210, Omnipaque 240, Omnipaque 300, Omnipaque 350

Patent coverage: 3,826 distinct patent families (11,605 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

9 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
myocardial ischemia3MONDO:0024644EFO:1001375
acute kidney injury2MONDO:0002492HP:0001919
kidney disorder2MONDO:0005240EFO:0003086
HIV infectious disease1MONDO:0005109EFO:0000764
kidney failure1MONDO:0001106HP:0000083
breast neoplasm1MONDO:0021100MONDO:0007254
neoplasm1MONDO:0005070EFO:0000616
Fabry disease1MONDO:0010526MONDO:0010526

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 62.

Phase distribution

PhaseTrials
Not specified22
PHASE117
PHASE411
PHASE34
PHASE24
EARLY_PHASE14

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05967117PHASE4RECRUITINGChest CT Using Low-concentration Iodine Contrast Media
NCT06709521PHASE4RECRUITINGOptimization of Beta-lactam Dosing in Critically Ill Patients With Cystatin C (OPTIMIZE-GNI)
NCT00478556PHASE4COMPLETEDOmnipaque Versus Gastroview as Oral Contrast for Abdominal and Pelvic CT
NCT02246998PHASE4COMPLETEDRenal Effect of Stribild or Other Tenofovir DF-containing Regimens Compared to Ritonavir-boosted Atazanavir Plus Abacavir/Lamivudine in Antiretroviral Treatment-naive HIV-1 Infected Adults
NCT02522338PHASE4COMPLETEDMeasurement of Glomerular Filtration Rate (GFR) in HIV Patients: Single-center Study Comparing the Accuracy of Estimators of GFR Versus Iohexol Plasma Clearance
NCT03415997PHASE4COMPLETEDDosing Iodinated Contrast Media According to Lean vs. Total Body Weight
NCT03631771PHASE4WITHDRAWNPediatric Risk of Hypothyroidism With Iodinated Contrast Media
NCT04113109PHASE4COMPLETEDMechanisms Underlying Hypotensive Response to ARB/NEP Inhibition - Aim 2
NCT04649229PHASE4COMPLETEDMechanisms Underlying Hypotensive Response to ARB/NEP Inhibition - Aim 3
NCT04742816PHASE4COMPLETEDRenal Effects of Hormones/Biomarkers in Transgender PrEP Recipients
NCT05065073PHASE4UNKNOWNIso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
NCT01984411PHASE3COMPLETEDComparison of Vascular Access for Radial and Femoral Completion of Diagnostic Cardiac Catheterization
NCT02050269PHASE3COMPLETEDMeasuring the Plasma Clearance of Iohexol to Estimate Glomerular Filtration Rate in Intensive Care Unit Patients: Preliminary Feasibility Study
NCT02961478PHASE3UNKNOWNMeasurement of Iohexol Plasma Clearance in Patients Leaving ICU After Acute Renal Failure
NCT03689946PHASE3COMPLETEDEffect of Evolocumab on Coronary Atherosclerosis
NCT02772276PHASE2COMPLETEDPharmacokinetics of MB-102 and Use of the Non-invasive Optical Renal Function Monitor (ORFM) Device in Subjects With Normal and Impaired Renal Function and a Range of Skin Color Types
NCT04627831PHASE2WITHDRAWNComparison of Captisol-Enabled™ Iohexol and Omnipaque™ in Patients With Impaired Renal Function Undergoing Coronary Angiography
NCT05672134PHASE2COMPLETEDEvaluation of GeranylGeranylAcetone in Heart Failure With Preserved Ejection Fraction
NCT06820320PHASE2COMPLETEDOral Iohexol in the Management of Chylous Ascites After After Retroperitoneal or Extended Lymphadenectomy
NCT03997370PHASE1ACTIVE_NOT_RECRUITINGEvaluation of Dosing Procedures of Chemotherapy Treatment (Carboplatin) With the Contrast Agent Iohexol
NCT05065372PHASE1RECRUITINGMANATEE-T1D: Metformin ANd AutomaTEd Insulin Delivery System Effects on Renal Vascular Resistance, Insulin Sensitivity, and Cardiometabolic Function in Youth With Type 1 Diabetes
NCT01214993PHASE1COMPLETEDA Phase 1, Open Label, Placebo-Controlled Study to Evaluate the Effect of GSK1349572 on Iohexol and Para-Aminohippurate Clearance in Healthy Subjects
NCT01839526PHASE1TERMINATEDA Study of Renal Function in Treatment-naïve, Young Male Patients With Fabry Disease
NCT02098174PHASE1COMPLETEDPharmacokinetics of MP-3180 in Healthy Volunteers
NCT02098187PHASE1COMPLETEDPharmacokinetics of MP-3180 and Use of Noninvasive Fluorescence Detection Device in Healthy Volunteers
NCT02342925PHASE1COMPLETEDA Study of the Effect of RG1662 on Metformin in Healthy Volunteers
NCT02884089PHASE1COMPLETEDA Study of the Effect of Abemaciclib on Metformin and Iohexol in Healthy Participants
NCT03545087PHASE1WITHDRAWNA Study of Lanabecestat in Participants With Severe Kidney Impairment Compared to Healthy Participants
NCT03826602PHASE1COMPLETEDA Drug-Drug Interaction Study in Healthy Volunteers of the Effects of Tucatinib on Metformin
NCT04008992PHASE1COMPLETEDAn Ascending Dose Study of BMS-986259 to Study Safety in Healthy Participants
NCT04156750PHASE1COMPLETEDA Study of LY3556050 in Healthy Participants
NCT04504331PHASE1TERMINATEDStudy of Infigratinib in Combination With Tamoxifen in Hormone Receptor Positive, HER2 Negative, FGFR Altered Advanced Breast Cancer
NCT05105009PHASE1COMPLETEDFurosemide and Creatinine Tubular Stress Test in Order to Measure Proximal Tubule Residual Function
NCT05136963PHASE1UNKNOWNDevelopment of a Bayesian Estimator for Calculating Plasma Iohexol Clearance
NCT05580250PHASE1WITHDRAWNA Study of LY3526318 in Healthy Male Japanese Participants
NCT05615467PHASE1COMPLETEDA Study of Effect of LY3556050 on Metformin in Healthy Participants
NCT04126824EARLY_PHASE1ACTIVE_NOT_RECRUITINGEffect of Addition of Steroids on Duration of Analgesia
NCT05754749EARLY_PHASE1RECRUITINGComparison of CE-DBT and MRI in Patients With Known Breast Lesions
NCT06220214EARLY_PHASE1RECRUITINGNeoadjuvant Therapy and Contrast-enhanced Mammography for Early Stage Breast Cancer
NCT04199754EARLY_PHASE1TERMINATEDIV Contrast-Enhanced Cone Beam Computed Tomography (CBCT) in Radiotherapy

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).