Page last updated: 2024-11-04

ioxaglate

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

Description

Ioxaglic Acid: A low-osmolar, ionic contrast medium used in various radiographic procedures. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

ioxaglic acid : A benzenedicarboxamide compound having N-substituted carbamoyl groups at the 1- and 3-positions, iodo substituents at the 2-, 4- and 6-positions and an acetyl(methyl)amino group at the 5-position. [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]

Cross-References

ID SourceID
PubMed CID3742
CHEMBL ID1201291
CHEBI ID31718
SCHEMBL ID38073
MeSH IDM0011691

Synonyms (80)

Synonym
smr001233442
MLS002154135
BRD-K79124250-001-03-0
ioxaglic acid
3-{[n-({3-[acetyl(methyl)amino]-2,4,6-triiodo-5-[(methylamino)carbonyl]phenyl}carbonyl)glycyl]amino}-5-{[(2-hydroxyethyl)amino]carbonyl}-2,4,6-triiodobenzoic acid
hexabrix 160
n-(2-hydroxyethyl)-2,4,6-triiodo-5-(2-(2,4,6-triiodo-3-(n-methylacetamido)-5-(methylcarbamoyl)benzamido)acetamido)isophthalamic acid
benzoic acid, 3-((((3-(acetylmethylamino)-2,4,6-triiodo-5-((methylamino)carbonyl)benzoyl)amino)acetyl)amino)-5-(((2-hydroxyethyl)amino)carbonyl)-2,4,6-triiodo-
acido ioxaglico [inn-spanish]
einecs 261-560-1
p 286 (contrast medium)
acide ioxaglique [inn-french]
acidum ioxaglicum [inn-latin]
hexabrix 320
cas-59017-64-0
NCGC00016886-01
PRESTWICK3_001062
AB00514026
ioxaglic acid (jan/usp/inn)
hexabrix 320 (tn)
D01761
59017-64-0
PRESTWICK2_001062
SPBIO_002962
PRESTWICK1_001062
PRESTWICK0_001062
BSPBIO_001044
BPBIO1_001150
NCGC00016886-02
acide ioxaglique
ioxaglate
3-[(n-{3-[acetyl(methyl)amino]-2,4,6-triiodo-5-(methylcarbamoyl)benzoyl}glycyl)amino]-5-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid
acidum ioxaglicum
CHEBI:31718 ,
acido ioxaglico
HMS1571E06
3-[[2-[[3-[acetyl(methyl)amino]-2,4,6-triiodo-5-(methylcarbamoyl)benzoyl]amino]acetyl]amino]-5-(2-hydroxyethylcarbamoyl)-2,4,6-triiodobenzoic acid
HMS2098E06
CHEMBL1201291
p-286
tox21_110664
dtxcid703166
dtxsid5023166 ,
HMS2234I18
z40x7ei2af ,
hsdb 8077
ioxaglic acid [usan:usp:inn:ban:jan]
unii-z40x7ei2af
FT-0627285
ioxaglic acid [usan]
benzoic acid, 3-((((3-(acetylmethylamino)-2,4,6-triiodo-5-9((methylamino)carbonyl)benzoyl)amino)acetyl)amino)-5-(((2-hydroxyethyl)amino)carbonyl)-2,4,6-triiodo-
ioxaglic acid [who-dd]
n-(2-hydroxyethyl)-2,4,6-triiodo-5-[2-[2,4,6-triiodo-3-(n-methylacetamido)-5-(methylcarbamoyl)benzamido]acetamido]isophthalamic acid
ioxaglic acid [ep monograph]
ioxaglic acid [jan]
ioxaglic acid [usp monograph]
ioxaglate [vandf]
ioxaglic acid [usp-rs]
ioxaglic acid [mi]
ioxaglic acid [inn]
ioxaglic acid [mart.]
HMS3371K01
CCG-221062
SCHEMBL38073
W-111165
DB09313
sr-01000841818
SR-01000841818-2
HMS3715E06
Q6064817
ioxaglic acid (100 mg)
ioxaglic-acid
hexabrix 160; p 286
NCGC00016886-04
HY-106586
3-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodo-5-(2-{[2,4,6-triiodo-3-(methylcarbamoyl)-5-(n-methylacetamido)phenyl]formamido}acetamido)benzoic acid
EN300-19767823
CS-0026109
[(methylamino)carbonyl]benzoyl]amino]acetyl]amino]-5-[[(2-hydroxyethyl)amino]carbonyl]-2,4,6-triiodo-
AKOS040758216

Research Excerpts

Overview

Ioxaglate is a well tolerated cardiac angiographic contrast agent that produces less hemodynamic disturbance than diatrizoate. It is an ionic contrast medium, popular because of its low osmolality.

ExcerptReferenceRelevance
"Ioxaglate is a well tolerated cardiac angiographic contrast agent that produces less hemodynamic disturbance than diatrizoate."( Hemodynamic changes induced by cardiac angiography with ioxaglate: comparison with diatrizoate.
Groh, WC; Hirshfeld, JW; Laskey, W; Martin, JL; Untereker, W; Wolf, GL, 1983
)
1.23
"Ioxaglate is an ionic contrast medium, popular because of its low osmolality."( Controlled, double-blind study of iosimide, a new, nonionic, monomeric contrast medium, and ioxaglate in cerebral angiography.
Aulich, A; Lenzner, A; Mull, M; Schwartz, A, 1989
)
1.22

Actions

Ioxaglate did not cause significant changes in urinary albumin concentrations. Evidence of platelet activation by iohexol and iopamidol was found in blood from two and three healthy volunteers, respectively.

ExcerptReferenceRelevance
"Ioxaglate did not cause any major adverse effects; side effects were rare and mild."( Clinical experience with ioxaglate (Hexabrix) in selective coronary arteriography.
Bonan, R; Bourassa, MG; Corcos, T; David, PR; Lespérance, J; Paquet, E, 1984
)
1.29
"Ioxaglate did not cause significant changes in urinary albumin concentrations (median concentration after angiography = 0.022 g/g creatinine)."( Subjective responses and albuminuria induced by ioxaglate during renal angiography in man.
Holtås, SL; Nilsson, PE; Tejler, LT, 1982
)
1.24
"Ioxaglate did not activate platelets, but evidence of platelet activation by iohexol and iopamidol was found in blood from two and three healthy volunteers, respectively, of the six volunteers studied. "( Activation of platelets by low-osmolar contrast media: differential effects of ionic and nonionic agents.
Hardeman, MR; Konijnenberg, A; Reekers, JA; Sturk, A, 1994
)
1.73

Treatment

ExcerptReferenceRelevance
"Ioxaglate-treated patients had a significantly lower renal failure incidence (0.8%, P<0.001)."( Renal failure in 57 925 patients undergoing coronary procedures using iso-osmolar or low-osmolar contrast media.
Hansell, P; Lagerqvist, B; Liss, P; Persson, PB, 2006
)
1.06

Toxicity

iopentol induces less postprocedural pain. Mild adverse events were observed more frequently in ioxaglate angiography.

ExcerptReferenceRelevance
" This difference was obscured in the previous studies by the pooling of RCTs in which the less toxic NIM were used and RCTs in which the more toxic ionic contrast medium ioxaglate was used."( Miscellaneous adverse effects of low-versus high-osmolality contrast media: a study revised.
Brismar, J; Jacobsson, BF; Jorulf, H, 1991
)
0.48
" The observed toxic effects were markedly potentiated by concomitant hypoxia."( Comparison of toxicity of radiocontrast agents to renal tubule cells in vitro.
Cieslinski, DA; Humes, HD; Messana, JM, 1990
)
0.28
" Mechanisms of severe adverse reactions are reviewed, including the views of Lasser and Lalli, and the view that emphasizes the importance of cardiotoxic and hemodynamic effects."( Chemotoxicity of contrast media and clinical adverse effects: a review.
Dawson, P,
)
0.13
" Hyperosmolality accounted for a major part of the cell toxicity, but additional toxic effects of the substances were observed."( Cytotoxic effects of six angiographic contrast media on human endothelium in culture.
Laerum, F,
)
0.13
"Nephrotoxicity of radio-opaque contrast media (CM) is generally believed to involve toxic injury of proximal tubular cells."( Nephrotoxicity of high- and low-osmolality contrast media.
Avila, A; Dennis, B; Finnie, KJ; Jevnikar, AM; Linton, AL; Plummer, DT, 1988
)
0.27
" No neurologic complications or adverse reactions requiring treatment occurred in either group."( Safety and efficacy of sodium and meglumine ioxaglate (Hexabrix) and Hypaque M60% in contrast-enhanced computed cranial tomographic scanning. A double-blind clinical study.
Czervionke, L; Dommers, M; Huckman, MS; James, ME; Ramsey, RG; Russell, EJ, 1987
)
0.53
" There was no difference in adverse side effects."( A double-blind clinical study comparing the safety and efficacy of Hexabrix and Renografin-76 in contrast enhanced computed body tomography.
DiSantis, DJ; James, M; Lee, JK; McClennan, BL,
)
0.13
"In several series of experiments with intracardiac application in anaesthetized dogs, the following contrast media were tested for their adverse effects on excitation and conduction of electrical activity in the heart."( Contrast media-induced side effects on excitation and conduction of electrical activity in the heart on intracardiac application. Investigations in anaesthetized dogs.
Diletti, E; Felix, R; Hahn, N; Logemann, N; Mählmann, J; Pantenburg, R; Potthoff, E; Raqué, B; Schmidt, I; Schuppert, J; Siering, T; Steinijans, V; Stiemert, D, 1981
)
0.26
"Because of the small number of visceral angiography procedures performed (38), no definitive conclusions could be drawn as to the differences between ionic and nonionic agents regarding grade-2 and grade-3 adverse events."( Safety of nonionic agents in visceral angiography.
Enge, IP, 1993
)
0.29
" Safety was evaluated by recording discomfort and other adverse events, changes in ECG, heart rate and blood pressure, changes in intra-arterial blood pressure and circulation time."( A double-blind study comparing safety, tolerability and efficacy of iodixanol 320 mgI/ml and ioxaglate 320 mgI/ml in cerebral arteriography.
De Greef, D; Grynne, BH; Palmers, Y; Put, E; Smits, J, 1993
)
0.51
" Outcome variables were pain, image quality and adverse events."( [Contrast media in peripheral angiography: does cost reduction mean loss of quality and safety? A reevaluation based on a randomized double-blind comparative study of ioxaglate versus iopromide].
Farres, MT; Lammer, J; Thurnher, S; Wildling, R; Winkelbauer, F; Woessmer, B, 1996
)
0.49
" Mild adverse events were observed more frequently in ioxaglate angiography (11% vs."( [Contrast media in peripheral angiography: does cost reduction mean loss of quality and safety? A reevaluation based on a randomized double-blind comparative study of ioxaglate versus iopromide].
Farres, MT; Lammer, J; Thurnher, S; Wildling, R; Winkelbauer, F; Woessmer, B, 1996
)
0.74
" However, an increase of mild adverse reactions up to 11% to 15% has to be accepted."( [Contrast media in peripheral angiography: does cost reduction mean loss of quality and safety? A reevaluation based on a randomized double-blind comparative study of ioxaglate versus iopromide].
Farres, MT; Lammer, J; Thurnher, S; Wildling, R; Winkelbauer, F; Woessmer, B, 1996
)
0.49
" 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
)
0.72
" 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
)
0.56
" 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
)
0.56
" 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
)
0.56
"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
)
0.9
" With regards to cell viability, transmonolayer resistance and inulin permeability the radiocontrast agents with reduced osmolality were significantly less toxic than diatrizoate, independent of their ionic strength."( Comparative cytotoxicity of ionic and non-ionic radiocontrast agents on MDCK cell monolayers in vitro.
Haller, C; Schick, CS, 1999
)
0.3

Pharmacokinetics

ExcerptReferenceRelevance
" Various pharmacokinetic parameters were calculated."( Pharmacokinetic study of ioxaglate, a low osmolality contrast medium, in patients with renal failure.
Bourin, M; Guenzet, J; Langlois, S; Laporte, V; Pengloan, J; Rouleau, P, 1986
)
0.57
" Some computed tomographic (CT) implications of these pharmacokinetic studies are discussed."( Pharmacokinetics of contrast media: experimental results in dog and man with CT implications.
Berger, N; Gardeur, D; Lautrou, J; Metzger, J; Millard, JC, 1980
)
0.26

Bioavailability

ExcerptReferenceRelevance
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51

Dosage Studied

ExcerptRelevanceReference
"At a given radiation dosage and field of view, five variables are under meaningful control for intravenous digital subtraction angiography (IV-DSA): concentration and quantity of contrast media injected, volume of injectate, rate of injection, and site of injection."( An experimental evaluation of central vs. peripheral injection for intravenous digital subtraction angiography (IV-DSA).
Bradley, BR; Brody, WR; Burbank, FH; Rubin, DL,
)
0.13
" Dosage was adjusted for patient weight, and up to 150-ml of Hexabrix or Renografin-76 were injected over a 2-minute period during which rapid sequence CT was performed."( Double-blind comparison of Hexabrix and Renografin-76 in computed tomography.
Berland, LL,
)
0.13
" The incidence of eosinophilia was irrespective of dosage or type of RCM."( Eosinophilia caused by iodinated radiographic contrast media.
Kuzmanić, D; Plavsić, B; Rotkvić, I, 1983
)
0.27
" The CAs were administered intravenously at a dosage of 4 g iodine/kg body weight."( The effect of iodinated contrast agent properties on renal kinetics and oxygenation.
Frisk, AL; Jost, G; Lengsfeld, P; Lenhard, DC; Pietsch, H, 2013
)
0.39
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
radioopaque mediumA substance having the property of absorbing, and therefore being opaque to, electromagnetic radiation, particularly X-rays.
[role 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]

Drug Classes (3)

ClassDescription
organoiodine compoundAn organoiodine compound is a compound containing at least one carbon-iodine bond.
benzenedicarboxamide
benzoic acidsAny aromatic carboxylic acid that consists of benzene in which at least a single hydrogen has been substituted by a carboxy group.
[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]

Protein Targets (3)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Beta-lactamaseEscherichia coli K-12Potency0.63100.044717.8581100.0000AID485294
pregnane X nuclear receptorHomo sapiens (human)Potency31.62280.005428.02631,258.9301AID1346985
IDH1Homo sapiens (human)Potency9.20000.005210.865235.4813AID686970
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (39)

Assay IDTitleYearJournalArticle
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID1079947Comments (NB not yet translated). [column 'COMMENTAIRES' in source]
AID1079946Presence of at least one case with successful reintroduction. [column 'REINT' in source]
AID1079949Proposed mechanism(s) of liver damage. [column 'MEC' in source]
AID1079936Choleostatic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is < 2 (see ACUTE). Value is number of references indexed. [column 'CHOLE' in source]
AID1079933Acute liver toxicity defined via clinical observations and clear clinical-chemistry results: serum ALT or AST activity > 6 N or serum alkaline phosphatases activity > 1.7 N. This category includes cytolytic, choleostatic and mixed liver toxicity. Value is
AID1079940Granulomatous liver disease, proven histopathologically. Value is number of references indexed. [column 'GRAN' in source]
AID1079938Chronic liver disease either proven histopathologically, or through a chonic elevation of serum amino-transferase activity after 6 months. Value is number of references indexed. [column 'CHRON' in source]
AID1079948Times to onset, minimal and maximal, observed in the indexed observations. [column 'DELAI' in source]
AID1079934Highest frequency of acute liver toxicity observed during clinical trials, expressed as a percentage. [column '% AIGUE' in source]
AID1079935Cytolytic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is > 5 (see ACUTE). Value is number of references indexed. [column 'CYTOL' in source]
AID1079939Cirrhosis, proven histopathologically. Value is number of references indexed. [column 'CIRRH' in source]
AID1079932Highest frequency of moderate liver toxicity observed during clinical trials, expressed as a percentage. [column '% BIOL' in source]
AID1079945Animal toxicity known. [column 'TOXIC' in source]
AID1079941Liver damage due to vascular disease: peliosis hepatitis, hepatic veno-occlusive disease, Budd-Chiari syndrome. Value is number of references indexed. [column 'VASC' in source]
AID1079931Moderate liver toxicity, defined via clinical-chemistry results: ALT or AST serum activity 6 times the normal upper limit (N) or alkaline phosphatase serum activity of 1.7 N. Value is number of references indexed. [column 'BIOL' in source]
AID1079943Malignant tumor, proven histopathologically. Value is number of references indexed. [column 'T.MAL' in source]
AID1079937Severe hepatitis, defined as possibly life-threatening liver failure or through clinical observations. Value is number of references indexed. [column 'MASS' in source]
AID1079944Benign tumor, proven histopathologically. Value is number of references indexed. [column 'T.BEN' in source]
AID1079942Steatosis, proven histopathologically. Value is number of references indexed. [column 'STEAT' in source]
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (769)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990310 (40.31)18.7374
1990's289 (37.58)18.2507
2000's103 (13.39)29.6817
2010's61 (7.93)24.3611
2020's6 (0.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.94

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 Index30.94 (24.57)
Research Supply Index6.99 (2.92)
Research Growth Index4.27 (4.65)
Search Engine Demand Index43.69 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials204 (23.18%)5.53%
Reviews19 (2.16%)6.00%
Case Studies48 (5.45%)4.05%
Observational0 (0.00%)0.25%
Other609 (69.20%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]