Iohexol
drugOn 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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1200455 |
| Name | Iohexol |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 3730 |
| ChEBI | CHEBI:31709 |
| ATC | V08AB02 |
| Molecular formula | C19H26I3N3O9 |
| Molecular weight | 821.1 |
| InChIKey | NTHXOOBQLCIOLC-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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| myocardial ischemia | 3 | MONDO:0024644 | EFO:1001375 |
| acute kidney injury | 2 | MONDO:0002492 | HP:0001919 |
| kidney disorder | 2 | MONDO:0005240 | EFO:0003086 |
| HIV infectious disease | 1 | MONDO:0005109 | EFO:0000764 |
| kidney failure | 1 | MONDO:0001106 | HP:0000083 |
| breast neoplasm | 1 | MONDO:0021100 | MONDO:0007254 |
| neoplasm | 1 | MONDO:0005070 | EFO:0000616 |
| Fabry disease | 1 | MONDO:0010526 | MONDO: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
| Phase | Trials |
|---|---|
| Not specified | 22 |
| PHASE1 | 17 |
| PHASE4 | 11 |
| PHASE3 | 4 |
| PHASE2 | 4 |
| EARLY_PHASE1 | 4 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05967117 | PHASE4 | RECRUITING | Chest CT Using Low-concentration Iodine Contrast Media |
| NCT06709521 | PHASE4 | RECRUITING | Optimization of Beta-lactam Dosing in Critically Ill Patients With Cystatin C (OPTIMIZE-GNI) |
| NCT00478556 | PHASE4 | COMPLETED | Omnipaque Versus Gastroview as Oral Contrast for Abdominal and Pelvic CT |
| NCT02246998 | PHASE4 | COMPLETED | Renal 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 |
| NCT02522338 | PHASE4 | COMPLETED | Measurement of Glomerular Filtration Rate (GFR) in HIV Patients: Single-center Study Comparing the Accuracy of Estimators of GFR Versus Iohexol Plasma Clearance |
| NCT03415997 | PHASE4 | COMPLETED | Dosing Iodinated Contrast Media According to Lean vs. Total Body Weight |
| NCT03631771 | PHASE4 | WITHDRAWN | Pediatric Risk of Hypothyroidism With Iodinated Contrast Media |
| NCT04113109 | PHASE4 | COMPLETED | Mechanisms Underlying Hypotensive Response to ARB/NEP Inhibition - Aim 2 |
| NCT04649229 | PHASE4 | COMPLETED | Mechanisms Underlying Hypotensive Response to ARB/NEP Inhibition - Aim 3 |
| NCT04742816 | PHASE4 | COMPLETED | Renal Effects of Hormones/Biomarkers in Transgender PrEP Recipients |
| NCT05065073 | PHASE4 | UNKNOWN | Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography |
| NCT01984411 | PHASE3 | COMPLETED | Comparison of Vascular Access for Radial and Femoral Completion of Diagnostic Cardiac Catheterization |
| NCT02050269 | PHASE3 | COMPLETED | Measuring the Plasma Clearance of Iohexol to Estimate Glomerular Filtration Rate in Intensive Care Unit Patients: Preliminary Feasibility Study |
| NCT02961478 | PHASE3 | UNKNOWN | Measurement of Iohexol Plasma Clearance in Patients Leaving ICU After Acute Renal Failure |
| NCT03689946 | PHASE3 | COMPLETED | Effect of Evolocumab on Coronary Atherosclerosis |
| NCT02772276 | PHASE2 | COMPLETED | Pharmacokinetics 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 |
| NCT04627831 | PHASE2 | WITHDRAWN | Comparison of Captisol-Enabled™ Iohexol and Omnipaque™ in Patients With Impaired Renal Function Undergoing Coronary Angiography |
| NCT05672134 | PHASE2 | COMPLETED | Evaluation of GeranylGeranylAcetone in Heart Failure With Preserved Ejection Fraction |
| NCT06820320 | PHASE2 | COMPLETED | Oral Iohexol in the Management of Chylous Ascites After After Retroperitoneal or Extended Lymphadenectomy |
| NCT03997370 | PHASE1 | ACTIVE_NOT_RECRUITING | Evaluation of Dosing Procedures of Chemotherapy Treatment (Carboplatin) With the Contrast Agent Iohexol |
| NCT05065372 | PHASE1 | RECRUITING | MANATEE-T1D: Metformin ANd AutomaTEd Insulin Delivery System Effects on Renal Vascular Resistance, Insulin Sensitivity, and Cardiometabolic Function in Youth With Type 1 Diabetes |
| NCT01214993 | PHASE1 | COMPLETED | A Phase 1, Open Label, Placebo-Controlled Study to Evaluate the Effect of GSK1349572 on Iohexol and Para-Aminohippurate Clearance in Healthy Subjects |
| NCT01839526 | PHASE1 | TERMINATED | A Study of Renal Function in Treatment-naïve, Young Male Patients With Fabry Disease |
| NCT02098174 | PHASE1 | COMPLETED | Pharmacokinetics of MP-3180 in Healthy Volunteers |
| NCT02098187 | PHASE1 | COMPLETED | Pharmacokinetics of MP-3180 and Use of Noninvasive Fluorescence Detection Device in Healthy Volunteers |
| NCT02342925 | PHASE1 | COMPLETED | A Study of the Effect of RG1662 on Metformin in Healthy Volunteers |
| NCT02884089 | PHASE1 | COMPLETED | A Study of the Effect of Abemaciclib on Metformin and Iohexol in Healthy Participants |
| NCT03545087 | PHASE1 | WITHDRAWN | A Study of Lanabecestat in Participants With Severe Kidney Impairment Compared to Healthy Participants |
| NCT03826602 | PHASE1 | COMPLETED | A Drug-Drug Interaction Study in Healthy Volunteers of the Effects of Tucatinib on Metformin |
| NCT04008992 | PHASE1 | COMPLETED | An Ascending Dose Study of BMS-986259 to Study Safety in Healthy Participants |
| NCT04156750 | PHASE1 | COMPLETED | A Study of LY3556050 in Healthy Participants |
| NCT04504331 | PHASE1 | TERMINATED | Study of Infigratinib in Combination With Tamoxifen in Hormone Receptor Positive, HER2 Negative, FGFR Altered Advanced Breast Cancer |
| NCT05105009 | PHASE1 | COMPLETED | Furosemide and Creatinine Tubular Stress Test in Order to Measure Proximal Tubule Residual Function |
| NCT05136963 | PHASE1 | UNKNOWN | Development of a Bayesian Estimator for Calculating Plasma Iohexol Clearance |
| NCT05580250 | PHASE1 | WITHDRAWN | A Study of LY3526318 in Healthy Male Japanese Participants |
| NCT05615467 | PHASE1 | COMPLETED | A Study of Effect of LY3556050 on Metformin in Healthy Participants |
| NCT04126824 | EARLY_PHASE1 | ACTIVE_NOT_RECRUITING | Effect of Addition of Steroids on Duration of Analgesia |
| NCT05754749 | EARLY_PHASE1 | RECRUITING | Comparison of CE-DBT and MRI in Patients With Known Breast Lesions |
| NCT06220214 | EARLY_PHASE1 | RECRUITING | Neoadjuvant Therapy and Contrast-enhanced Mammography for Early Stage Breast Cancer |
| NCT04199754 | EARLY_PHASE1 | TERMINATED | IV 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.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: myocardial ischemia