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Details

Stereochemistry MIXED
Molecular Formula C17H22I3N3O8
Molecular Weight 777.0853
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IOMEPROL

SMILES

CN(C(=O)CO)C1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)NCC(O)CO)=C1I

InChI

InChIKey=NJKDOADNQSYQEV-UHFFFAOYSA-N
InChI=1S/C17H22I3N3O8/c1-23(9(29)6-26)15-13(19)10(16(30)21-2-7(27)4-24)12(18)11(14(15)20)17(31)22-3-8(28)5-25/h7-8,24-28H,2-6H2,1H3,(H,21,30)(H,22,31)

HIDE SMILES / InChI

Molecular Formula C17H22I3N3O8
Molecular Weight 777.0853
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description is created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/10852647

Iomeprol is a nonionic, monomeric iodinated contrast medium. Iomeprol helps optimize images obtained with sophisticated multidetector computed tomography (MDCT) technology, especially for neurological, brain, liver, cardiac and vascular scanning. The mechanism of action of Iomeprol is as a X-Ray Contrast Activity. Launched by the Bracco Group in 1995, Iomeprol (Iomeron) currently is registered in more than 40 countries worldwide, including all major European markets, Japan, and major Middle East and Asian Pacific countries.

CNS Activity

Curator's Comment: Iomeprol penetrates into the brain of dogs

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
Iomeprol

Approved Use

For cerebral angiography

Launch Date

1992
Diagnostic
Iomeprol

Approved Use

For intravenous urography

Launch Date

1992
Diagnostic
Iomeprol

Approved Use

For Angiocardiography

Launch Date

1992
PubMed

PubMed

TitleDatePubMed
[Multidetector CT Angiography - is it a valuable screening tool to detect significant renal artery stenosis?].
2001 Dec
Ionic and non-ionic contrast agent-mediated endothelial injury. Quantitative analysis of cell proliferation during endothelial repair.
2001 Jul
Four-dimensional cardiac imaging with multislice computed tomography.
2001 Mar 27
[Doppler evaluation of thyroid hemodynamics after intravenous administration of contrast media].
2001 Nov-Dec
Coronary angiography using 4 or 6 French diagnostic catheters: a prospective, randomized study.
2001 Oct
Ozonation: a tool for removal of pharmaceuticals, contrast media and musk fragrances from wastewater?
2003 Apr
Three-dimensional CT angiography of the hepatic artery: use of multi-detector row helical CT and a contrast agent.
2003 Jun
Advances in vascular and cardiac MDCT imaging: peripheral arteries.
2003 Nov
Advances in cardiac imaging.
2003 Nov
Fate of pharmaceuticals--photodegradation by simulated solar UV-light.
2003 Sep
Multislice computed tomography angiography of the abdominal arteries: comparison between computed tomography angiography and digital subtraction angiography findings in 52 cases.
2004 Jun
Solitary pulmonary nodules: dynamic enhanced multi-detector row CT study and comparison with vascular endothelial growth factor and microvessel density.
2004 Oct
Analysis of iodinated X-ray contrast agents in water samples by ion chromatography and inductively-coupled plasma mass spectrometry.
2005 Aug 26
Multiphase contrast-enhanced CT of the liver with a multislice CT scanner: effects of iodine concentration and delivery rate.
2005 Feb
MDCT angiography of the pulmonary arteries: influence of iodine flow concentration on vessel attenuation and visualization.
2005 Jun
Cross-flow microfiltration with periodical back-washing for photocatalytic degradation of pharmaceutical and diagnostic residues-evaluation of the long-term stability of the photocatalytic activity of TiO2.
2005 Mar
Does iodine concentration affect the diagnostic efficacy of biphasic spiral CT in patients with hepatocellular carcinoma?
2005 May-Jun
Demonstration of cardiac involvement of sarcoidosis by contrast-enhanced multislice computed tomography and delayed-enhanced magnetic resonance imaging.
2005 Nov-Dec
Multidetector CT in abdominal aortic aneurysm treated with endovascular repair: are unenhanced and delayed phase enhanced images effective for endoleak detection?
2006 Dec
16-MDCT aortography with a low-dose contrast material protocol.
2006 Feb
Characterization of acute and chronic myocardial infarcts by multidetector computed tomography: comparison with contrast-enhanced magnetic resonance.
2006 Feb 14
Acute pulmonary embolism to the subsegmental level: diagnostic accuracy of three MRI techniques compared with 16-MDCT.
2006 Jul
Multislice computed tomography and magnetic resonance imaging for the assessment of reperfused acute myocardial infarction.
2006 Jul 4
Imaging of aortopulmonary collateral arteries with high-resolution multidetector CT.
2006 Jun
Improving diagnostic accuracy of MDCT coronary angiography in patients with mild heart rhythm irregularities using ECG editing.
2006 Mar
High iodine concentration contrast material for noninvasive multislice computed tomography coronary angiography: iopromide 370 versus iomeprol 400.
2006 Mar
Drug eruptions to contrast media in Japan.
2006 May
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Can also be used intravascularly https://www.medicines.org.uk/emc/medicine/15853
IOMERON 300 Injection: each mL of IOMERON contains 612.4 mg (equivalent to 300 mg of iodine) of iomeprol. Radiological examination IOMERON 300 - 5 - 15 mL Thoracic angiography IOMERON 300 5 - 50 mL Abdominal angiography IOMERON 300 - 5 - 60 mL Peripheral anogiography IOMERON 300 - 10 - 80 mL Intravenous digital subtraction angiography IOMERON 300 - 10 - 50 mL Intraarterial digital subtraction angiography IOMERON 300 - 3 - 40 mL The dosage may be adjusted depending on the patient’s age, body weight, symptoms and purpose of use. In the case of multiple-dose administration, a total dosage of 250 mL should not be exceeded.
Route of Administration: Intravenous
In Vitro Use Guide
Iomeprol induced a time- and dose-dependent inhibition of MTT conversion in LLC-PK1-cells (75%-19% of control) at concentrations ranging from 4.7 to 75 mg I/mL after an incubation time of 2 hours and 64%-14% of control after 24 hours.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:10 GMT 2023
Edited
by admin
on Fri Dec 15 17:50:10 GMT 2023
Record UNII
17E17JBP8L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IOMEPROL
INN   JAN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
E-7337
Code English
N,N'-BIS(2,3-DIHYDROXYPROPYL)-2,4,6-TRIIODO-5-(N-METHYLGLYCOLAMIDO)ISOPHTHALAMIDE
Systematic Name English
IOMEPROL [MI]
Common Name English
IOMEPROL [JAN]
Common Name English
IOMERON 300
Brand Name English
iomeprol [INN]
Common Name English
E7337
Code English
Iomeprol [WHO-DD]
Common Name English
1,3-BENZENEDICARBOXAMIDE, N,N'-BIS(2,3-DIHYDROXYPROPYL)-5-((HYDROXYACETYL)METHYLAMINO)-2,4,6-TRIIODO-
Systematic Name English
IOMEPROL [USAN]
Common Name English
IOMEPROL [MART.]
Common Name English
Classification Tree Code System Code
WHO-ATC V08AB10
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
WHO-VATC QV08AB10
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
Code System Code Type Description
LACTMED
Iomeprol
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
NCI_THESAURUS
C166471
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
FDA UNII
17E17JBP8L
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
WIKIPEDIA
Iomeprol
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
PUBCHEM
3731
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
MESH
C057937
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
DAILYMED
17E17JBP8L
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
DRUG CENTRAL
1463
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
EVMPD
SUB08234MIG
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID1049061
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
CAS
78649-41-9
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
USAN
BB-15
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
MERCK INDEX
m6367
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY Merck Index
RXCUI
2606484
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PRIMARY
DRUG BANK
DB11705
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107214
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
CHEBI
31710
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
SMS_ID
100000083083
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
INN
5859
Created by admin on Fri Dec 15 17:50:10 GMT 2023 , Edited by admin on Fri Dec 15 17:50:10 GMT 2023
PRIMARY
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