Page last updated: 2024-12-06

iopentol

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID56016
CHEMBL ID2104783
CHEBI ID135893
SCHEMBL ID24471
MeSH IDM0151714

Synonyms (34)

Synonym
iopentolum [latin]
IOPENTOL ,
imagopaque
n,n'-bis(2,3-dihydroxypropyl)-5-(n-(2-hydroxy-3-methoxypropyl)acetamido)-2,4,6-triiodoisophthalamide
1,3-benzenedicarboxamide, 5-(acetyl(2-hydroxy-3-methoxypropyl)amino)-n,n'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-
iopentol (usan/inn)
D04582
89797-00-2
CHEBI:135893
5-[acetyl-(2-hydroxy-3-methoxypropyl)amino]-1-n,3-n-bis(2,3-dihydroxypropyl)-2,4,6-triiodobenzene-1,3-dicarboxamide
7d6xwx076t ,
cpd. 5411
iopentolum
unii-7d6xwx076t
iopentol [usan:inn:ban]
FT-0627282
cpd-5411
CHEMBL2104783
SCHEMBL24471
iopentol [mart.]
iopentol [inn]
iopentol [usan]
iopentol [who-dd]
iopentol [mi]
n,n'-bis(2,3-dihydroxypropyl)-5-[n-(2-hydroxy-3-methoxypropyl)acetamido]-2,4,6-triiodoisophthalamide
IUNJANQVIJDFTQ-UHFFFAOYSA-N
1-n,3-n-bis(2,3-dihydroxypropyl)-5-[n-(2-hydroxy-3-methoxypropyl)acetamido]-2,4,6-triiodobenzene-1,3-dicarboximidic acid
Q6063892
DB13861
MS-31552
DTXSID40869032
CS-0377801
HY-142121
iodixanol related compound d(50 mg)(5-[acetyl(2-hydroxy-3-methylpropyl)amino]-n,n'-bis(2,3-dihydroxypropyl)2,4,6-triiodo-1,3-benze-nedicarboxamide)

Research Excerpts

Overview

Iopentol is a new non-ionic, water-soluble ratio 3.0 roentgen contrast medium (CM) for vascular use. It induced a short-lasting imbalance of the microcirculation already in vascular regions not affected by atherosclerosis.

ExcerptReferenceRelevance
"Iopentol-350 is a high-viscous Xray contrast medium and induced a short-lasting imbalance of the microcirculation already in vascular regions not affected by atherosclerosis."( Influence of a radiographic contrast media (Iopentol) with different viscosities on capillary perfusion in patients with coronary artery disease.
Franke, RP; Gerk, U; Jung, F; Mrowietz, C, 2013
)
1.37
"Iopentol was shown to be a safe and effective contrast medium in examinations of children."( A double-blind CT study comparing the safety and efficacy of iopentol and ioxaglate in paediatric patients.
Baraton, J; Lallemand, D; Nantois, C; Porée, C; Sayegh, N; Skinningsrud, K, 1996
)
1.26
"Iopentol is a new non-ionic contrast medium. "( Pharmacokinetics of iopentol in healthy volunteers.
Andrew, E; Jørgensen, NP; Koksvik, B; Skinnemoen, K; Waaler, A, 1987
)
2.04
"Iopentol is a new non-ionic monomeric intravascular radiologic contrast medium which is undergoing clinical trials. "( Effect of iopentol on acetylcholinesterase activity and thrombin time. Comparative studies.
Dawson, P, 1987
)
2.12
"Iopentol is a new nonionic, water-soluble ratio 3.0 roentgen contrast medium (CM) for vascular use. "( Clinical trial program for iopentol. A new nonionic ratio 3.0 contrast medium with emphasis on clinical phases I and II.
Andrew, E; Bach-Gansmo, T; Holager, T; Jakobsen, J; Kruger Hagen, E; Lambrechts, M; Moxnes, A; Waaler, A, 1988
)
2.01

Toxicity

Both iopentol and ioxaglate are effective and safe contrast media for use in knee arthrography, but iopENTol induces less postprocedural pain.

ExcerptReferenceRelevance
"The low osmolar, non-ionic X-ray contrast media have shown a lower frequency of adverse events than the older ionic ones."( Safety and tolerability of iodixanol in healthy volunteers with reference to two monomeric X-ray contrast media.
Borch, KW; Jørgensen, NP; Kristiansen, AB; Kristoffersen, DT; Lundby, B; Nossen, JO; Theodorsen, L, 1992
)
0.28
" Adverse events, hemodynamic parameters, and clinical chemical parameters in the blood and urine were recorded."( Safety and toleration of the non-ionic contrast medium iopentol. An intravenous phase I trial.
Aakhus, T; Andrew, E; Hagve, TA; Haider, T; Holager, T; Jakobsen, JA; Waaler, A, 1989
)
0.52
" Approximate intravenous LD50 values in mice have been determined for the remaining compounds."( Synthesis, analysis and toxicity of some compounds which may be formed during the synthesis of iopentol.
Aulie Michelet, A; Berg, A; Dugstad, H; Fagervoll, R, 1987
)
0.49
" Serious adverse events did not occur in either group."( Image quality and safety in pediatric urography using an ionic and a non-ionic iodinated contrast agent.
Brekke, O; Kristofferssen, DT; Mortensson, W; Nybonde, T; Wahlgren, H, 1994
)
0.29
" There was a total of 18 patients who reported adverse events other than sensations of heat or cold, 6 (13%) in the iopentol group and 12 (27%) in the ioxaglate group."( A double-blind CT study comparing the safety and efficacy of iopentol and ioxaglate in paediatric patients.
Baraton, J; Lallemand, D; Nantois, C; Porée, C; Sayegh, N; Skinningsrud, K, 1996
)
0.74
"3%) experienced one or more adverse events."( Iopentol (Imagopaque) in vascular procedures. A multi-centre monitoring trial assessing adverse events and diagnostic information--results from 3,587 patients in Germany.
Grynne, BH; Henseke, P; Muth, CP, 1997
)
1.74
" Safety was evaluated by registering adverse events (AEs) reported by the patients, and data were analysed using a multiple factor model."( Evaluation of iopentol (Imagopaque 350) in CT enhancement. A multi-centre monitoring trial assessing adverse events and diagnostic information--results from 1,823 patients in France.
Bunouf, P; Lambrechts, M; Menuet, JF; Oxaal, M, 1997
)
0.66
" Specifically, frequency of adverse events (AEs), subjective change in quality of diagnostic information, and quantitative enhancement characteristics were compared."( Iopentol (Imagopaque 300) compared with iopromide (Ultravist 300) in abdominal CT. A multi-centre monitoring trial assessing adverse events and diagnostic information--results from 518 patients in Spain.
Encina, JL; Martí-Bonmatí, L; Rodríguez, V; Ronchera-Oms, CL, 1997
)
1.74
" No adverse events were observed among the children below 1 year of age."( Iopentol (Imagopaque 300) compared with iohexol (Omnipaque 300) and diatrizoate (Urografin 292) in pediatric urography. A clinical trial assessing adverse events and diagnostic information.
Brekke, O; Lanning, P, 1997
)
1.74
" There were no statistically significant differences between numbers of patients reporting adverse events nor number of patients reporting discomfort in the two groups."( Iopentol (Imagopaque 350) compared with iohexol (Omnipaque 350) in pediatric cardioangiography. A clinical trial assessing adverse events, ECG, blood pressure and diagnostic information.
De Greef, D; Kunnen, M; Skinningsrud, K, 1997
)
1.74
" ECG, blood pressure, heart rate, adverse events and efficacy were evaluated."( Iopentol (Imagopaque 300) compared with iopromide (Ultravist 300) in pediatric angiocardiography. A clinical trial assessing adverse events, ECG and diagnostic information.
Aggoun, Y; Iserin, L; Kachaner, J; Piéchaud, JF; Skinningsrud, K, 1997
)
1.74
" Safety was assessed by monitoring serum pancreatic iso-amylase and by recording adverse events."( Iopentol (Imagopaque 250) compared with diatrizoate (Urografin 219) in endoscopic retrograde cholangio-pancreatography (ERCP). A clinical trial assessing safety (adverse events and S-pancreatic iso-amylase) and diagnostic information (VAS).
Bjartveit, K; Brock, A; Kruse, A; Nowakowska-Duawa, E; Rodenberg, J, 1997
)
1.74
" Other adverse events and radiographic efficacy were also evaluated."( Iopentol (Imagopaque 300) compared with ioxaglate (Hexabrix 320) in knee arthrography. A clinical trial assessing immediate and late adverse events and diagnostic information.
Brekke, O; Railhac, JJ, 1997
)
1.74
" Immediate adverse events were recorded up to 30 min post-injection, and late adverse events, including knee pain and swelling, up to 4 days after the examination (by using a patient questionnaire)."( Iopentol (Imagopaque 300) compared with ioxaglate (Hexabrix 320) in knee arthrography. A clinical trial assessing immediate and late adverse events and diagnostic information.
Brekke, O; Railhac, JJ, 1997
)
1.74
" Adverse events up to 30 min after the examination, and late adverse events other than knee pain, were reported by similar numbers of patients in the two contrast medium groups."( Iopentol (Imagopaque 300) compared with ioxaglate (Hexabrix 320) in knee arthrography. A clinical trial assessing immediate and late adverse events and diagnostic information.
Brekke, O; Railhac, JJ, 1997
)
1.74
"Both iopentol and ioxaglate are effective and safe contrast media for use in knee arthrography, but iopentol induces less postprocedural pain."( Iopentol (Imagopaque 300) compared with ioxaglate (Hexabrix 320) in knee arthrography. A clinical trial assessing immediate and late adverse events and diagnostic information.
Brekke, O; Railhac, JJ, 1997
)
2.25
" Safety was evaluated by assessing the numbers of patients reporting immediate adverse events (up to 30 min after injection) and delayed adverse events (within 7 days after the examination)."( Iopentol (Imagopaque 350) compared with diatrizoate (Urografin 370) in cerebral CT. A clinical trial assessing immediate and late (7 days) adverse events and diagnostic information (visualization quality and Hounsfield unit measurements).
Jakobsen, JA; Klaveness, AJ; Valentine, A, 1997
)
1.74
" Two patients (5%) in each group reported contrast-related adverse events other than a sensation of heat, while three patients in the iopentol group and four in the iohexol group reported procedure-related adverse events."( Iopentol (Imagopaque 300 and 350) compared with iohexol (Omnipaque 300 and 350) in cerebral and aortic arch angiography. A clinical trial assessing adverse events and diagnostic information.
Bjartveit, K; Ericsson, K, 1997
)
1.94

Pharmacokinetics

iopentol 350 mg I/ml was administered intravenously to healthy male volunteers at 3 dose levels (0.3, 0.4 and 0.5 mg) The pharmacokinetic properties and potential metabolism of iopentOL have been investigated after intravenous injection in rats.

ExcerptReferenceRelevance
" Mean elimination half-life was 28."( Pharmacokinetics of iopentol in patients with chronic renal failure.
Berg, KJ; Kolmannskog, F; Lillevold, PE; Nordal, KP; Ressem, L; Svaland, MG, 1992
)
0.61
"The pharmacokinetic properties and potential metabolism of iopentol have been investigated after intravenous injection in rats."( Pharmacokinetics of iopentol in the rat.
Michelet, AA; Skinnemoen, K, 1987
)
0.84
" In order to study the pharmacokinetic properties, iopentol 350 mg I/ml was administered intravenously to healthy male volunteers at 3 dose levels (0."( Pharmacokinetics of iopentol in healthy volunteers.
Andrew, E; Jørgensen, NP; Koksvik, B; Skinnemoen, K; Waaler, A, 1987
)
0.85

Dosage Studied

ExcerptRelevanceReference
" The dosage of contrast medium (350 mg I/ml) was 700 mg I/kg body weight."( Renal effects of iopentol and iohexol after intravenous injection.
Berg, KJ; Jakobsen, JA; Kolbenstvedt, AN, 1991
)
0.62
" In the case of iopentol, a dose-response study was performed, 1 ml x 3 and 4 ml x 3 being also tested."( The influence of non-ionic contrast media on the endothelium of small arteries. A comparison of metrizamide, iohexol and iopentol.
Stjernquist, U; Wieslander, JB, 1987
)
0.83
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
amidobenzoic acid
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (103)

TimeframeStudies, This Drug (%)All Drugs %
pre-199026 (25.24)18.7374
1990's57 (55.34)18.2507
2000's15 (14.56)29.6817
2010's5 (4.85)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 21.00

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index21.00 (24.57)
Research Supply Index5.04 (2.92)
Research Growth Index4.40 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.00)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials41 (36.28%)5.53%
Reviews5 (4.42%)6.00%
Case Studies4 (3.54%)4.05%
Observational0 (0.00%)0.25%
Other63 (55.75%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]