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glucaric acid

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Description

Glucaric acid is a dicarboxylic acid that is a naturally occurring compound found in plants and animals. It has been studied for its potential health benefits, including its role in glucose metabolism and its antioxidant properties. Glucaric acid is synthesized in the body from glucose through the uronic acid pathway. Research has indicated that glucaric acid may have potential for treating conditions such as diabetes and obesity. It has been found to inhibit the absorption of glucose in the intestine and to promote insulin sensitivity. Glucaric acid is also being investigated as a potential anticancer agent due to its ability to inhibit the growth of certain cancer cells. The study of glucaric acid continues to explore its potential as a therapeutic agent for various conditions, including diabetes, obesity, and cancer.'

Glucaric Acid: A sugar acid derived from D-glucose in which both the aldehydic carbon atom and the carbon atom bearing the primary hydroxyl group are oxidized to carboxylic acid groups. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

D-glucaric acid : The D-enantiomer of glucaric acid. [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]

glucaric acid : A hexaric acid derived by oxidation of sugar such as glucose with nitric acid. [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 CID33037
CHEMBL ID1794737
CHEBI ID16002
SCHEMBL ID5496
MeSH IDM0009320

Synonyms (44)

Synonym
glucaric acid, d-
CHEBI:16002 ,
d-(+)-saccharic acid
saccharic acid
(2r,3s,4s,5s)-2,3,4,5-tetrahydroxyhexanedioic acid
87-73-0
glucaric acid
d-glucosaccharic acid
C00818
saccharate
d-saccharic acid
l-gularic acid
d-saccharate
d-glucaric acid
D-GLUCARATE ,
GKR ,
DB03603
52B6CA34-55ED-41A0-BE2A-45AABDC4DC81
(2s,3s,4s,5r)-2,3,4,5-tetrahydroxyhexanedioic acid
BMSE000239
2s,3s,4s,5r-tetrahydroxy-hexanedioic acid
LMFA01170108
qlz991v4a2 ,
unii-qlz991v4a2
einecs 201-768-1
dl-glucaric acid
25525-21-7
d-glucaric acid [mi]
d-tetrahydroxyadipic acid
glucaric acid [inci]
SCHEMBL5496
DSLZVSRJTYRBFB-LLEIAEIESA-N
d-glucosaccharate
l-gularate
d-tetrahydroxyadipate
d-(+)-saccharate
DTXSID60859455
Q424636
glucaric-acid
CHEMBL1794737
D83869
DTXSID501340165
d-glucosaccharicacid
CS-0456843

Research Excerpts

Overview

D-Glucaric acid (GA) is a major value-added chemicals feedstock and additive. It is used in the food, cosmetics, and pharmaceutical industries. D-glucarIC acid is a natural non-toxic compound produced in small amounts by mammals, including humans.

ExcerptReferenceRelevance
"D-glucaric acid is a promising platform compound used to synthesize many other value-added or commodity chemicals. "( Biosynthesis of D-glucaric acid from sucrose with routed carbon distribution in metabolically engineered Escherichia coli.
Fan, LH; Guo, Q; Li, JL; Qu, YN; Ruan, YC; Tan, TW; Yan, HJ; Yue, XZ; Zheng, WX, 2018
)
1.54
"Glucaric acid is a high-value-added chemical that can be used in various fields. "( Metabolic engineering of Saccharomyces cerevisiae for efficient production of glucaric acid at high titer.
Chen, N; Deng, Y; Wang, J; Zhao, Y, 2018
)
2.15
"Glucaric acid (GA) is a major value-added chemicals feedstock and additive, especially in the food, cosmetics, and pharmaceutical industries. "( Efficient Bioconversion of Sucrose to High-Value-Added Glucaric Acid by In Vitro Metabolic Engineering.
Guo, ZW; Li, N; Lou, WY; Su, HH; Wu, XL; Xu, P; Zong, MH, 2019
)
2.2
"d-Glucaric acid (GA) is an aldaric acid and consists of an asymmetric acyclic sugar backbone with a carboxyl group positioned at either end of its structure (i.e., the C1 and C6 positions). "( Conformation analysis of d-glucaric acid in deuterium oxide by NMR based on its JHH and JCH coupling constants.
Enomoto-Rogers, Y; Furihata, K; Ito, T; Iwata, T; Masaki, H, 2016
)
1.45
"D-glucaric acid is a natural non-toxic compound produced in small amounts by mammals, including humans. "( [The biological role of D-glucaric acid and its derivatives: potential use in medicine].
Hanausek, M; Kiliańska, ZM; Walaszek, Z; Zółtaszek, R, 2008
)
1.37
"D-Glucaric acid (GA) is a nontoxic, natural compound. "( Metabolism, uptake, and excretion of a D-glucaric acid salt and its potential use in cancer prevention.
Adams, AK; Hanausek, M; Kilgore, J; Narog, M; Sherman, U; Szemraj, J; Walaszek, Z, 1997
)
1.28
"D-Glucaric acid is a natural, non-toxic compound produced in small amounts by mammals, including humans."( Potential use of D-glucaric acid derivatives in cancer prevention.
Walaszek, Z, 1990
)
1.17

Effects

D-Glucaric acid (GlucA) has been identified as one of the top 10 potential bio-based chemicals for replacement of oil-basedchemicals. D-glucARic acid has been explored for a myriad of potential uses, including biopolymer production and cancer treatment.

ExcerptReferenceRelevance
"Glucaric acid (GlucA) has been identified as one of the top 10 potential bio-based chemicals for replacement of oil-based chemicals. "( Mixed-mode liquid chromatography for the rapid analysis of biocatalytic glucaric acid reaction pathways.
Bergquist, PL; Care, A; Petroll, K; Sunna, A; Waterstraat, M, 2019
)
2.19
"D-glucaric acid has been explored for a myriad of potential uses, including biopolymer production and cancer treatment. "( Improving D-glucaric acid production from myo-inositol in E. coli by increasing MIOX stability and myo-inositol transport.
Prather, KL; Shiue, E, 2014
)
1.5
"D-Glucaric acid has been found in many vegetables and fruits."( Detoxifying cancer causing agents to prevent cancer.
Hanausek, M; Slaga, TJ; Walaszek, Z, 2003
)
0.88

Toxicity

ExcerptReferenceRelevance
" During the maintenance phase (period of epoetin therapy after correction of iron deficiency), the use of low-dose intravenous iron supplementation (10 to 20 mg per haemodialysis treatment or 100 mg every second week) avoids iron overtreatment and minimises potential adverse effects."( Safety aspects of parenteral iron in patients with end-stage renal disease.
Hörl, WH; Sunder-Plassmann, G, 1997
)
0.3
" We prospectively examined adverse events and vital signs after administering 100 mg of IV iron sucrose in each of 10 consecutive dialysis treatment sessions and compared results with those recorded in each of three consecutive dialysis sessions without iron treatment."( Safety and efficacy of iron sucrose in patients sensitive to iron dextran: North American clinical trial.
Adhikarla, R; Cavallo, G; Charytan, C; Gagnon, S; Levin, N; Spinowitz, BS; Van Wyck, DB, 2000
)
0.31
" This drug has been associated with occasional serious adverse reactions, including full-blown anaphylaxis."( The comparative safety of intravenous iron dextran, iron saccharate, and sodium ferric gluconate.
Fishbane, S; Kowalski, EA,
)
0.13
" We assessed safety by recording blood pressure and adverse events after iron sucrose injection and comparing results with those for the same patients during an observation control period."( Efficacy and safety of iron sucrose for iron deficiency in patients with dialysis-associated anemia: North American clinical trial.
Al-Saloum, M; Charytan, C; Gagnon, S; Hafeez, T; Levin, N; Van Wyck, DB, 2001
)
0.31
" Of the IV iron preparations available, iron sucrose has proved its efficacy and safety; however, there are no guidelines or systematic studies examining the optimum safe dosage regimen for this compound."( Intravenous iron sucrose: establishing a safe dose.
Chandler, G; Harchowal, J; Macdougall, IC, 2001
)
0.31
" None of patient discontinued the therapy due to any adverse effect."( Comparative study--efficacy, safety and compliance of intravenous iron sucrose and intramuscular iron sorbitol in iron deficiency anemia of pregnancy.
Mushtaq, A; Wali, A, 2002
)
0.31
"Administration of 250 mg SFGC over 1 hour is safe and well tolerated."( Chronic use of sodium ferric gluconate complex in hemodialysis patients: safety of higher-dose (> or =250 mg) administration.
Agarwal, R; Coyne, DW; Dahl, N; Folkert, VW; Michael, B; Myirski, P; Warnock, DG, 2003
)
0.32
" Two patients had seven adverse events that were considered related to iron sucrose."( The safety and efficacy of an accelerated iron sucrose dosing regimen in patients with chronic kidney disease.
Avram, MM; Blaustein, DA; Chattopadhyay, J; Daoui, R; Gadh, R; Schwenk, MH; Singh, H, 2003
)
0.32
"An accelerated regimen of high-dose intravenous iron sucrose therapy in CKD patients is safe and effective in restoring iron stores, and may potentially save time and improve patient adherence."( The safety and efficacy of an accelerated iron sucrose dosing regimen in patients with chronic kidney disease.
Avram, MM; Blaustein, DA; Chattopadhyay, J; Daoui, R; Gadh, R; Schwenk, MH; Singh, H, 2003
)
0.32
"There were no serious adverse events related to iron sucrose therapy in the 130 patients intolerant to other iron preparations."( Safety of iron sucrose in hemodialysis patients intolerant to other parenteral iron products.
Al-Saloum, MM; Charytan, C; Schwenk, MH; Spinowitz, BS, 2004
)
0.32
"Iron sucrose therapy is safe and well tolerated in hemodialysis patients intolerant to iron dextran and/or sodium ferric gluconate."( Safety of iron sucrose in hemodialysis patients intolerant to other parenteral iron products.
Al-Saloum, MM; Charytan, C; Schwenk, MH; Spinowitz, BS, 2004
)
0.32
" Safety and tolerability of the therapy was assessed by the occurrence of adverse events under therapy and up to one week after completion of the study."( A study for the evaluation of safety and tolerability of intravenous high-dose iron sucrose in patients with iron deficiency anemia due to gastrointestinal bleeding.
Blumenstein, I; Dignass, AU; Jahnel, J; Schröder, O; Schrott, M; Stein, J, 2004
)
0.32
"A total of 14 adverse events were observed in 10 patients, of which two adverse events in two patients were considered as being definitely related to drug administration."( A study for the evaluation of safety and tolerability of intravenous high-dose iron sucrose in patients with iron deficiency anemia due to gastrointestinal bleeding.
Blumenstein, I; Dignass, AU; Jahnel, J; Schröder, O; Schrott, M; Stein, J, 2004
)
0.32
"A single intravenous high-dose iron sucrose therapy in patients with IDA due to gastrointestinal blood loss appears to be safe and therefore is a therapeutic option which may save time and improve patient compliance."( A study for the evaluation of safety and tolerability of intravenous high-dose iron sucrose in patients with iron deficiency anemia due to gastrointestinal bleeding.
Blumenstein, I; Dignass, AU; Jahnel, J; Schröder, O; Schrott, M; Stein, J, 2004
)
0.32
" However, serious adverse events have been reported after single doses of some intravenous iron products."( Iron sucrose in hemodialysis patients: safety of replacement and maintenance regimens.
Aronoff, GR; Bennett, WM; Blumenthal, S; Charytan, C; Pennell, JP; Reed, J; Rothstein, M; Strom, J; Van Wyck, D; Wolfe, A; Yee, J, 2004
)
0.32
" With each dosing regimen, adverse events, if any, were recorded and described."( Iron sucrose in hemodialysis patients: safety of replacement and maintenance regimens.
Aronoff, GR; Bennett, WM; Blumenthal, S; Charytan, C; Pennell, JP; Reed, J; Rothstein, M; Strom, J; Van Wyck, D; Wolfe, A; Yee, J, 2004
)
0.32
" There were no serious or life-threatening drug-related adverse events."( Iron sucrose in hemodialysis patients: safety of replacement and maintenance regimens.
Aronoff, GR; Bennett, WM; Blumenthal, S; Charytan, C; Pennell, JP; Reed, J; Rothstein, M; Strom, J; Van Wyck, D; Wolfe, A; Yee, J, 2004
)
0.32
"Iron sucrose is safe when given as treatment for iron deficiency or for maintenance of iron stores."( Iron sucrose in hemodialysis patients: safety of replacement and maintenance regimens.
Aronoff, GR; Bennett, WM; Blumenthal, S; Charytan, C; Pennell, JP; Reed, J; Rothstein, M; Strom, J; Van Wyck, D; Wolfe, A; Yee, J, 2004
)
0.32
"We have not observed any adverse reactions upon iron administration."( [Safety and usefulness of parenteral iron in the management of anemia due to hip fracture in the elderly].
Cuenca Espiérrez, J; García Erce, JA; Martínez Martín, AA; Modrego Aranda, FJ; Solano, VM, 2004
)
0.32
"Parenteral administration of iron could be a safe and effective way to avoid or reduce allogeneic blood transfusions in THF patients."( [Safety and usefulness of parenteral iron in the management of anemia due to hip fracture in the elderly].
Cuenca Espiérrez, J; García Erce, JA; Martínez Martín, AA; Modrego Aranda, FJ; Solano, VM, 2004
)
0.32
"To define the adverse events following two different rates and methods of intravenous iron sucrose infusions in children with anaemia due to chronic renal impairment."( Low incidence of adverse events following 90-minute and 3-minute infusions of intravenous iron sucrose in children on erythropoietin.
Anbu, AT; Bradbury, MG; Kemp, T; O'donnell, K; Smith, PA, 2005
)
0.33
"Two prospective observational studies were undertaken to characterize the adverse events following iron sucrose administration in children with renal impairment and on erythropoietin."( Low incidence of adverse events following 90-minute and 3-minute infusions of intravenous iron sucrose in children on erythropoietin.
Anbu, AT; Bradbury, MG; Kemp, T; O'donnell, K; Smith, PA, 2005
)
0.33
" Sixty-five doses were administered over 3 min to 20 children, and six minor adverse events were documented."( Low incidence of adverse events following 90-minute and 3-minute infusions of intravenous iron sucrose in children on erythropoietin.
Anbu, AT; Bradbury, MG; Kemp, T; O'donnell, K; Smith, PA, 2005
)
0.33
"Although 90 min infusion is associated with fewer adverse events, no life-threatening events were documented in either method."( Low incidence of adverse events following 90-minute and 3-minute infusions of intravenous iron sucrose in children on erythropoietin.
Anbu, AT; Bradbury, MG; Kemp, T; O'donnell, K; Smith, PA, 2005
)
0.33
" Variables evaluated in the intent-to-treat population included adverse events (AEs), hemoglobin, and iron indices."( The safety of intravenous iron sucrose use in the elderly patient.
Charytan, C; Reed, J; Yee, J, 2007
)
0.34
"Serious adverse events that occur with the administration of iron dextran are due to the high molecular weight preparations."( Low-molecular weight iron dextran and iron sucrose have similar comparative safety profiles in chronic kidney disease.
Al Talib, K; Auerbach, M, 2008
)
0.35
"To describe the efficacy and adverse effects of intravenous iron sucrose therapy in a group of children with iron deficiency anemia who did not respond to oral iron therapy."( Efficacy and safety of intravenous iron sucrose therapy in a group of children with iron deficiency anemia.
Kapelushnik, J; Levy, J; Moser, A; Pinsk, V; Yerushalmi, B, 2008
)
0.35
" One patient demonstrated a severe side effect with temporary and reversible reduced blood pressure during treatment."( Efficacy and safety of intravenous iron sucrose therapy in a group of children with iron deficiency anemia.
Kapelushnik, J; Levy, J; Moser, A; Pinsk, V; Yerushalmi, B, 2008
)
0.35
"These preliminary data suggest that administration of intravenous iron in pediatric patients is well tolerated and has a good clinical result, with minimal adverse reactions."( Efficacy and safety of intravenous iron sucrose therapy in a group of children with iron deficiency anemia.
Kapelushnik, J; Levy, J; Moser, A; Pinsk, V; Yerushalmi, B, 2008
)
0.35
"45% per patient) and a total of 56 adverse events (1."( The comparative safety of various intravenous iron preparations in chronic kidney disease patients.
Anirban, G; Gupta, KL; Jha, V; Kohli, HS; Sakhuja, V, 2008
)
0.35
" There were tolerable adverse events in both groups."( Safety and usefulness of intravenous iron sucrose in the management of preoperative anemia in patients with menorrhagia: a phase IV, open-label, prospective, randomized study.
Chung, HH; Kang, SB; Kim, SC; Kim, YH; Kim, YT, 2009
)
0.35
"Preoperative intravenous iron sucrose administration is more effective than oral iron and is as safe as oral iron therapy in the correction of preoperative anemia due to menorrhagia."( Safety and usefulness of intravenous iron sucrose in the management of preoperative anemia in patients with menorrhagia: a phase IV, open-label, prospective, randomized study.
Chung, HH; Kang, SB; Kim, SC; Kim, YH; Kim, YT, 2009
)
0.35
"Iron sucrose and low-molecular-weight iron dextran (LMW-ID), two commonly used iron solutions, have been compared in terms of allergic adverse event profiles to date."( Safety profiles of total dose infusion of low-molecular-weight iron dextran and high-dose iron sucrose in renal patients.
Acar, K; Atalay, H; Govec, N; Solak, Y; Turk, S, 2011
)
0.37
"Spontaneously-reported rates of adverse events (AEs) of intravenous (i."( Differences in spontaneously reported hypersensitivity and serious adverse events for intravenous iron preparations: comparison of Europe and North America.
Bailie, GR; Hörl, WH; Verhoef, JJ, 2011
)
0.37
" Safety and tolerability of both groups were compared on the basis of reported systemic and local adverse events."( Safety and efficacy of high-dose intravenous iron carboxymaltose vs. iron sucrose for treatment of postpartum anemia.
Christoph, P; Pfenniger, A; Schuller, C; Surbek, D, 2012
)
0.38
"Rapid administration of high ICM doses was as well tolerated as IS with overall adverse events of 5% (ICM) vs."( Safety and efficacy of high-dose intravenous iron carboxymaltose vs. iron sucrose for treatment of postpartum anemia.
Christoph, P; Pfenniger, A; Schuller, C; Surbek, D, 2012
)
0.38
"IV ICM is as safe as IS in the management of postpartum (IDA) iron deficiency anemia despite five times of higher dosage."( Safety and efficacy of high-dose intravenous iron carboxymaltose vs. iron sucrose for treatment of postpartum anemia.
Christoph, P; Pfenniger, A; Schuller, C; Surbek, D, 2012
)
0.38
" Among 619 unique patients who received IV iron over a 2-year period, we found 32 adverse events (AEs), ranging from urticaria to chest pain."( Comparative rates of adverse events with different formulations of intravenous iron.
Abel, GA; Hevelone, N; Mandell, E; Okam, MM; Ross, A; Wentz, R, 2012
)
0.38
"We assessed adverse event rates between dosing groups."( Comparison of the safety and efficacy of 3 iron sucrose iron maintenance regimens in children, adolescents, and young adults with CKD: a randomized controlled trial.
Goldstein, SL; Morris, D; Warady, BA, 2013
)
0.39
" No differences were noted between regimens in reported adverse effects, which were all minor."( Comparison of the safety and efficacy of 3 iron sucrose iron maintenance regimens in children, adolescents, and young adults with CKD: a randomized controlled trial.
Goldstein, SL; Morris, D; Warady, BA, 2013
)
0.39
" Post several months of use we observed increased rates of adverse events from patients and hence performed this analysis to confirm these findings."( Comparison of adverse event profile of intravenous iron sucrose and iron sucrose similar in postpartum and gynecologic operative patients.
Choi, GY; Kim, JS; Lee, ES; Lee, IS; Lee, JJ; Park, BR, 2013
)
0.39
"Data on adverse events was retrospectively collected from 658 patients treated between September 2004 and December 2011."( Comparison of adverse event profile of intravenous iron sucrose and iron sucrose similar in postpartum and gynecologic operative patients.
Choi, GY; Kim, JS; Lee, ES; Lee, IS; Lee, JJ; Park, BR, 2013
)
0.39
" Adverse drug reactions were more frequent in the ISS(FRX) groups vs."( Comparison of adverse event profile of intravenous iron sucrose and iron sucrose similar in postpartum and gynecologic operative patients.
Choi, GY; Kim, JS; Lee, ES; Lee, IS; Lee, JJ; Park, BR, 2013
)
0.39
"This is the first large analysis suggesting increased adverse events due to an ISS."( Comparison of adverse event profile of intravenous iron sucrose and iron sucrose similar in postpartum and gynecologic operative patients.
Choi, GY; Kim, JS; Lee, ES; Lee, IS; Lee, JJ; Park, BR, 2013
)
0.39
" However, parenteral iron supplementation is usually safe and without major side effects."( [Safety aspects of parenteral iron supplementation therapies in patients with chronic kidney disease].
Münch, HG; Potthoff, SA, 2013
)
0.39

Pharmacokinetics

ExcerptReferenceRelevance
" Pharmacokinetic parameters of phenobarbital and parahydroxyphenobarbital were determined from plasma and urine samples obtained after 28 days of daily administration of 100 mg phenobarbital and after a further 9 days of phenobarbital plus 2400 mg/day felbamate or placebo."( Effects of felbamate on the pharmacokinetics of phenobarbital.
Banfield, CR; Colucci, RD; Glue, P; Guillaume, M; Lin, CC; Meehan, JW; Mojavarian, P; Nezamis, J; Radwanski, E; Reidenberg, P, 1995
)
0.29
" Development of these pharmaceutical agents requires pharmacokinetic studies monitoring levels of both the administered agent and transferrin-bound iron (TBI)."( Analysis of total and transferrin-bound iron in human serum for pharmacokinetic studies of iron-sucrose formulations.
Burrows, DM; Corcoran, HF; Dotzauer, H; Goggin, MM; Gozum, SD; Janis, GC; Lundberg, RA; Nguyen, A; Tann, CM, 2011
)
0.37

Compound-Compound Interactions

ExcerptReferenceRelevance
") once per week for 5 doses in combination with 2,000 international units (IU) EPO (Eprex, Cilag-Janssen), subcutaneously given simultaneously also for 5 doses."( The effect of i.v. iron alone or in combination with low-dose erythropoietin in the rapid correction of anemia of chronic renal failure in the predialysis period.
Agbaria, Z; Baruch, R; Blum, M; Deutsch, V; Iaina, A; Irony, M; Schwartz, D; Silverberg, DS; Steinbruch, S; Yachnin, T, 2001
)
0.31
"In IBD patients with refractory anaemia the administration of darbepoetin in combination with intravenous iron sucrose can raise haemoglobin levels."( Effectiveness of darbepoetin-alfa in combination with intravenous iron sucrose in patients with inflammatory bowel disease and refractory anaemia: a pilot study.
Karmiris, K; Kouroumalis, EA; Koutroubakis, IE; Makreas, S; Niniraki, M; Xidakis, C, 2006
)
0.33
" by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography."( Isolation of three glucaric acids from Leonurus japonicus Houtt. by using high-speed countercurrent chromatography combined with semi-preparative high-performance liquid chromatography.
Hu, P; Jia, Q; Kang, L; Li, Y; Li, Z; Liu, Y; Zhang, H; Zhang, M, 2022
)
1.05

Bioavailability

ExcerptReferenceRelevance
"The effect of liver enzyme induction on bioavailability of hetacillin was studied in patients chronically treated with anticonvulsants or chlorpromazine."( Effect of enzyme induction on bioavailability of hetacillin in patients treated with anticonvulsants and chlorpromazine.
Dimakopoulou, K; Galanopoulou, P; Karageorgiou, C,
)
0.13
" Oral iron administration with appraisable bioavailability was able to compensate blood losses up to 151 and with increasing doses up to 361 per year with maintenance of normal or borderline haemoglobin values."( [Chronic hemorrhagic iron deficiency. Sources of hemorrhage, blood loss and systematic iron substitution].
Balling, A; Hausmann, K; Kuse, R, 1987
)
0.27
" This enzyme induction most likely contributes to the decreased bioavailability observed upon co-administration of various drugs with Saint John's wort extract."( Differential effects of Saint John's Wort (hypericum perforatum) on the urinary excretion of D-glucaric acid and 6beta-hydroxycortisol in healthy volunteers.
Bauer, S; Brockmöller, J; Johne, A; Kerb, R; Roots, I; Störmer, E, 2002
)
0.53
" Calcium D-glucarate is promoted as an orally bioavailability dietary supplement with potential chemopreventive activity without adverse effects."( A comparative study of antioxidative activity of calcium-D-glucarate, sodium-D-gluconate and D-glucono-1,4-lactone in a human blood platelet model.
Saluk-Juszczak, J, 2010
)
0.36
" Oral iron is a low cost treatment however its effectiveness is limited by low bioavailability and poor tolerability."( State of the iron: how to diagnose and efficiently treat iron deficiency anemia in inflammatory bowel disease.
Bhandari, S; Muñoz, M; Reinisch, W; Staun, M, 2013
)
0.39
"Currently, most countries apply the standard generic approach for the approval of intended copies of originator nanoparticle iron medicinal products, requiring only demonstration of bioequivalence to a reference medicinal product by bioavailability studies."( Nanoparticle iron medicinal products - Requirements for approval of intended copies of non-biological complex drugs (NBCD) and the importance of clinical comparative studies.
Borchard, G; Flühmann, B; Mühlebach, S, 2012
)
0.38
"The bioavailability of Venofer® and ISA was investigated in both cell types by a ferrozin-based assay."( Bioavailability and stability of intravenous iron sucrose originator versus generic iron sucrose AZAD.
Cornelius, C; Goldenberg, H; Praschberger, M; Scheiber-Mojdehkar, B; Schitegg, M; Sturm, B, 2015
)
0.42
"ISA shows identical physico-chemical features and identical bioavailability in vitro."( Bioavailability and stability of intravenous iron sucrose originator versus generic iron sucrose AZAD.
Cornelius, C; Goldenberg, H; Praschberger, M; Scheiber-Mojdehkar, B; Schitegg, M; Sturm, B, 2015
)
0.42
" In conclusion, FCM has low bioavailability for liver parenchyma cells, therefore liver iron deposition is unlikely."( Iron sucrose and ferric carboxymaltose: no correlation between physicochemical stability and biological activity.
Cornelius, C; Goldenberg, H; Haider, K; Praschberger, M; Scheiber-Mojdehkar, B; Schitegg, M; Sturm, B, 2015
)
0.42
", enterohepatic, enteric and local recycling) plays a central role in governing the disposition of phenolics such as flavonoids, resulting in low systemic bioavailability but higher gut bioavailability and longer than expected apparent half-life."( Triple Recycling Processes Impact Systemic and Local Bioavailability of Orally Administered Flavonoids.
Dai, P; Hu, M; Li, Q; Liu, Z; Lu, L; Luo, F; Wang, L; Wang, X; Wang, Y; Zhu, L, 2015
)
0.42
" In vitro studies with Caco-2 cells suggested that newly synthesized microemulsions had better iron bioavailability as compared to commercially available iron dextran formulations."( Potential of Alginate Encapsulated Ferric Saccharate Microemulsions to Ameliorate Iron Deficiency in Mice.
Angmo, S; Mukhija, K; Sandhir, R; Singhal, K; Singhal, NK; Yadav, H; Yadav, K, 2016
)
0.43
" Oral iron is simple and cheap to administer and does not require hospital visits, but is poorly absorbed in advanced CKD and is associated with unpleasant gastrointestinal side effects."( Iron Treatment Strategies in Nondialysis CKD.
Macdougall, IC, 2016
)
0.43

Dosage Studied

Study was to investigate the relationship of changes in the enzyme-inducing anticonvulsant daily dosage (drug score) to variations in urinary D-glucaric acid excretion and gamma-glutamyltransferase and beta- glucuronidase serum activities.

ExcerptRelevanceReference
" An increase in post dosing urinary excretion of D-glucaric acid showed a correlation with the ratio of calculated to observed areas under the plasma concentration, time curve following the final dose in the multiple dosing studies, indicating that hepatic microsomal enzymes are induced after repeated administration of the drug."( The effect of repeated administration of diftalone on enzyme induction.
Franklin, C; Garnham, JC; Natunen, T; Saunders, L; Stainton-Ellis, DM; Turner, P; Volans, G, 1978
)
0.51
" When clinically indicated the daily dosage rate was adjusted by 50 mg steps until a serum concentration of 10--20 mg/l was produced."( Individual variation in daily dosage requirements for phenytoin sodium in patients with epilepsy.
Barot, MH; Grant, RH; Maheendran, KK; Mawer, GE; Woodcock, BG, 1978
)
0.26
"The applicability of a pharmacokinetic model for drug interactions by enzyme induction was tested by chronic dosing situation using carbamazepine (Tegretol) as the inducer and clonazepam (Clonopin) as the drug affected."( Time-course of interaction between carbamazepine and clonazepam in normal man.
Cutler, RE; Lai, AA; Levy, RH, 1978
)
0.26
" Protection was dosage related, and potentiated with increasing doses, but only when the two drugs were given simultaneously."( Protective effect of D-glucaro-delta-lactam against amino-glycoside-induced nephrotoxicity in rats.
Inouye, S; Koeda, T; Niida, T; Nizato, T; Tsuruoka, T, 1976
)
0.26
" We report the elevated excretion of D-glucaric acid (DGA) and D-glucuronic acid (GCA) following treatment with 2,7-difluorospirofluorene-9,5'-imidazolidine-2'4'-dione (Imirestat, IM, Al 1576, HOE 843) at 50 mg/kg/day for 1 month, but not with 3-4-bromo-2-fluorobenzyl-4-oxo-3-phthalazine-1-ylacetic acid (Ponalrestat, Statil), dosed at 50 mg/kg/day for 2 weeks."( Studies on the biochemical effects of the aldose reductase inhibitor 2,7-difluorospirofluorene-9,5'-imidazolidine-2',4'-dione (Al 1576, HOE 843). Detection of D-glucaric and D-glucuronic acid excretion by high resolution 1H and 13C NMR spectroscopy.
Gilbert, PJ; Hoyle, VR; Nicholson, JK; Troke, JA; Vose, CW, 1992
)
0.55
" The conventional urines exceeded the germ-free urines by 10-fold in their content of 6-hydroxy-1-acetamidopyrene (NAAP-6-OH), previously identified as the predominant contributor to the mutagenicity of the urines of rats dosed with NP and excreted mainly as its beta-glucuronide conjugate."( Formation of mutagenic urinary metabolites from 1-nitropyrene in germ-free and conventional rats: role of the gut flora.
Ball, LM; Gustafsson, BE; Gustafsson, JA; Kohan, MJ; Lewtas, J; Rafter, JJ, 1991
)
0.28
"Intramuscular administration of glucarolactam in the form of aminoglycoside salt to guinea-pigs protected the experimental ototoxicity caused by high dosing of aminoglycoside antibiotics."( Effect of glucarolactam on ototoxicity of aminoglycoside antibiotics in guinea-pigs.
Inouye, S; Kitasato, I; Niizato, T; Yokota, M, 1989
)
0.28
" The aim of our studies on patients with various chronic liver diseases was to get information about the rational dosage for these patients."( Investigation of biotransformation capacity in patients with chronic liver diseases by pharmacokinetic methods: experimental trials.
Horváth, T; Jávor, T; Kádas, I; Pár, A; Past, T; Tapsonyi, Z; Tatai, Z,
)
0.13
" Significant positive correlations were found between the dosage of CBZ, DPH, PMD and PB and both indices of enzyme induction."( A comparative study of the relative enzyme inducing properties of anticonvulsant drugs in epileptic patients.
Hedges, A; Makki, KA; Perucca, E; Richens, A; Ruprah, M; Wilson, JF, 1984
)
0.27
" The results have been evaluated from the methodological aspect to work out an appropriate dosage regime in liver diseases."( Correlation between biochemical tests, parameters of drug elimination and hepatic enzyme induction in chronic liver diseases.
Beró, T; Fábián, C; Horváth, T; Jávor, T; Kádas, I; Pár, A, 1983
)
0.27
" This dosage also induces the first and the second phases of reactions."( Human tolerance of flumecinol (Zixoryn, RGH-3332), its regime and dosage in healthy volunteers.
Ferenci, J; Horvath, T; Jávor, T; Nagy, L; Past, T; Radnai, B; Vezekenyi, Z, 1983
)
0.27
" Dose-response studies suggest that like retinoids, glucarate acts directly on tumor cells, rather than having an adjuvant effect."( Mechanism of growth inhibition of mammary carcinomas by glucarate and the glucarate: retinoid combination.
Abou-Issa, H; Curley, RC; Nguyen, MH; Stromberg, PC; Webb, TE,
)
0.13
") treatment with epoetin alfa 300 IU/kg twice weekly for 3 weeks was the optimum dosage for facilitation of AB donation and minimization of the decrease in Hct prior to elective orthopedic surgery."( Epoetin alfa for autologous blood donation in patients with rheumatoid arthritis and concomitant anemia.
Mercuriali, F, 1996
)
0.29
" Adequate intravenous iron supplementation allows reduction of epoetin dosage by approximately 40%."( Safety aspects of parenteral iron in patients with end-stage renal disease.
Hörl, WH; Sunder-Plassmann, G, 1997
)
0.3
" The dosage of iron was individually adapted according to a target hemoglobin level of 13 g/100 ml and to the actual lowest hemoglobin level measured."( [Intravenous iron in the treatment of postoperative anemia in surgery of the spine in infants and adolescents].
Bernière, J; Dehullu, JP; Gall, O; Murat, I, 1998
)
0.3
"Iron balance is critical for adequate erythropoiesis and there remains much debate concerning the optimal timing and dosage of iron therapy for haemodialysis patients receiving recombinant human erythropoietin therapy."( Enhanced oxidative stress in haemodialysis patients receiving intravenous iron therapy.
Kho, B; Lim, PS; Wei, YH; Yu, YL, 1999
)
0.3
"To determine the effect of different dosing schedules of intravenous iron therapy on the hematocrit level, we randomly assigned 18 patients to 3 groups."( Clinical characteristic of parenteral iron supplementation in hemodialysis patients receiving erythropoietin therapy.
Chang, HY; Chen, KS; Kao, HH; Lee, CC; Tsai, CJ, 2000
)
0.31
" To save manpower and costs, we recommend the large single dosing schedule."( Clinical characteristic of parenteral iron supplementation in hemodialysis patients receiving erythropoietin therapy.
Chang, HY; Chen, KS; Kao, HH; Lee, CC; Tsai, CJ, 2000
)
0.31
" iron preparations with respect to haemoglobin levels, iron status and recombinant human erythropoetin (rHuEpo) dosage requirements in stable, rHuEpo-treated haemodialysis patients (maintenance phase of iron treatment) over 6 months."( A randomized, controlled parallel-group trial on efficacy and safety of iron sucrose (Venofer) vs iron gluconate (Ferrlecit) in haemodialysis patients treated with rHuEpo.
Bahner, U; Bettger, H; Kosch, M; Matzkies, F; Schaefer, RM; Teschner, M, 2001
)
0.31
"5 ng/ml with iron gluconate), while rHuEpo dosage did not change significantly throughout the study."( A randomized, controlled parallel-group trial on efficacy and safety of iron sucrose (Venofer) vs iron gluconate (Ferrlecit) in haemodialysis patients treated with rHuEpo.
Bahner, U; Bettger, H; Kosch, M; Matzkies, F; Schaefer, RM; Teschner, M, 2001
)
0.31
" Of the IV iron preparations available, iron sucrose has proved its efficacy and safety; however, there are no guidelines or systematic studies examining the optimum safe dosage regimen for this compound."( Intravenous iron sucrose: establishing a safe dose.
Chandler, G; Harchowal, J; Macdougall, IC, 2001
)
0.31
"The purpose of this study was to investigate the relationship of changes in the enzyme-inducing anticonvulsant daily dosage (drug score) to variations in urinary D-glucaric acid excretion and gamma-glutamyltransferase and beta-glucuronidase serum activities."( Relationship between changes in drug score, D-glucaric acid excretion, and gamma-glutamyltransferase and beta-glucuronidase serum activities during anticonvulsant treatment.
Fernández, MP; Hermida, J; Tutor, JC, 2002
)
0.77
" Three patients had nonserious events that did not preclude further dosing of SFGC."( Chronic use of sodium ferric gluconate complex in hemodialysis patients: safety of higher-dose (> or =250 mg) administration.
Agarwal, R; Coyne, DW; Dahl, N; Folkert, VW; Michael, B; Myirski, P; Warnock, DG, 2003
)
0.32
" We summarize the advantages and disadvantages of each product, including risk of anaphylaxis and hypersensitivity, dosage regimens, and costs."( Parenteral iron therapy options.
Rodgers, GM; Silverstein, SB, 2004
)
0.32
"Isolated mouse proximal tubule segments (PTS) or cultured proximal tubular [human kidney (HK-2)] cells were exposed to four representative iron preparations [iron sucrose (FeS), iron dextran (FeD), iron gluconate (FeG), or iron oligosaccharide (FeOS)] over a broad dosage range (0, 30 to 1000 microg iron/mL)."( Parenteral iron nephrotoxicity: potential mechanisms and consequences.
Hanson, SY; Johnson, AC; Zager, RA, 2004
)
0.32
"In this safety study, iron sucrose was given in two dosing regimens."( Iron sucrose in hemodialysis patients: safety of replacement and maintenance regimens.
Aronoff, GR; Bennett, WM; Blumenthal, S; Charytan, C; Pennell, JP; Reed, J; Rothstein, M; Strom, J; Van Wyck, D; Wolfe, A; Yee, J, 2004
)
0.32
" Although peak serum concentrations of all compounds were inversely proportional to body weight, the percentage of change during dialysis was not related to dosage or body weight."( Effects of different dialysis membranes on serum concentrations of epoetin alfa, darbepoetin alfa, enoxaparin, and iron sucrose during dialysis.
Chester, K; McMahon, LP; Walker, RG, 2004
)
0.32
" The iron gluconate was given in a dosage of 62."( Intravenous iron in a primary-care clinic.
Maslovsky, I, 2005
)
0.33
"Administration of 200 mg of iron sucrose as an intravenous bolus injection over 2 minutes is a practical dosing regimen in patients with chronic kidney disease, resulting in considerable savings in time and cost."( Administration of intravenous iron sucrose as a 2-minute push to CKD patients: a prospective evaluation of 2,297 injections.
Macdougall, IC; Roche, A, 2005
)
0.33
"We performed a prospective multicentre clinical trial in iron-replete haemodialysis patients to evaluate the efficacy of weekly low-dose (50 mg) intravenous iron sucrose administration for 6 months to maintain the iron status, and to examine the effect on epoetin dosage needed to maintain stable haemoglobin values in these patients."( Weekly low-dose treatment with intravenous iron sucrose maintains iron status and decreases epoetin requirement in iron-replete haemodialysis patients.
Ambühl, PM; Binet, I; Dickenmann, M; Keusch, G; Lüthi, L; Schiesser, D; Schmidli, M; Tsinalis, D; Wüthrich, RP, 2006
)
0.33
"A regular 50 mg weekly dosing schedule of iron sucrose maintains stable iron stores and haemoglobin levels in haemodialysed patients and allows considerable dose reductions for epoetins."( Weekly low-dose treatment with intravenous iron sucrose maintains iron status and decreases epoetin requirement in iron-replete haemodialysis patients.
Ambühl, PM; Binet, I; Dickenmann, M; Keusch, G; Lüthi, L; Schiesser, D; Schmidli, M; Tsinalis, D; Wüthrich, RP, 2006
)
0.33
" Patients received IV iron sucrose therapy in treatment and maintenance dosing cycles over 10-week periods."( The safety of intravenous iron sucrose use in the elderly patient.
Charytan, C; Reed, J; Yee, J, 2007
)
0.34
" Iron needs and erythropoietin dosing were similar in both the elder and younger adult patients."( The safety of intravenous iron sucrose use in the elderly patient.
Charytan, C; Reed, J; Yee, J, 2007
)
0.34
" groups in terms of sex, age, duration of hemodialysis, dialysis frequency per week, EPO dosage per week, the level of intact parathyroid hormone, serum creatinine, blood urea nitrogen, or hematological parameters at baseline."( Intravenous iron sucrose in Chinese hemodialysis patients with renal anemia.
Li, H; Wang, SX, 2008
)
0.35
" Differences in iron formulation, dosing regiment, and peripheral iron status may explain some of the discrepancies between this and previous IV iron treatment studies."( A randomized, double-blind, placebo-controlled trial of intravenous iron sucrose in restless legs syndrome.
Allen, RP; Barker, PB; Beard, JL; Earley, CJ; Horská, A; Mohamed, MA, 2009
)
0.35
"There were no differences between the IV and oral groups in terms of sex, age, duration of PD, mean dialysate dosage per day, erythropoietin dosage per week, or hematological parameters at baseline."( Intravenous iron sucrose in peritoneal dialysis patients with renal anemia.
Li, H; Wang, SX,
)
0.13
" Further studies on target patient groups, dosing and dosing intervals are warranted before iron sucrose could be considered for treatment of iron deficient patients with RLS."( A randomized, double-blind, placebo controlled, multi-center study of intravenous iron sucrose and placebo in the treatment of restless legs syndrome.
Grote, L; Hedner, J; Leissner, L; Ulfberg, J, 2009
)
0.35
" ESA dosage used in the iron sucrose group at week 8 was significantly lower than in the Fe chloride group (244."( Comparison of parenteral iron sucrose and ferric chloride during erythropoietin therapy of haemodialysis patients.
Chen, HH; Chen, YC; Chuang, CK; Lee, KF; Lin, HC; Wu, CJ, 2010
)
0.36
"Although the differences in ESA dosage, ferritin and iron dosage between two groups were found during the study period while similar results were shown at the end of 24 week study."( Comparison of parenteral iron sucrose and ferric chloride during erythropoietin therapy of haemodialysis patients.
Chen, HH; Chen, YC; Chuang, CK; Lee, KF; Lin, HC; Wu, CJ, 2010
)
0.36
" However, there are no guidelines about safety limits in dosage amounts or intervals."( Postoperative high-dose intravenous iron sucrose with low dose erythropoietin therapy after total hip replacement.
Kim, S; Lee, SC; Lim, H; Yoon, J, 2010
)
0.36
" The outcomes of administering this dosage regimen are reported as observational retrospective analysis using patient record data in 2009."( Total dose infusion of intravenous iron in patients with chronic kidney disease receiving haemodialysis.
Fenwick, S; Peebles, G, 2011
)
0.37
" We aimed to compare adverse-effect profiles of LMW-ID and iron sucrose with varying dosing schedules in PD patients with a hope to foster use of parenteral iron solutions in PD patients."( Comparison of adverse-event profiles of intravenous low-molecular-weight iron dextran and iron sucrose in peritoneal dialysis patients.
Atalay, H; Guney, I; Kaya, E; Solak, Y; Turk, S; Turkmen, K, 2011
)
0.37
"The simpler FCM-based dosing regimen showed better efficacy and compliance, as well as a good safety profile, compared with the Ganzoni-calculated IS dose regimen."( FERGIcor, a randomized controlled trial on ferric carboxymaltose for iron deficiency anemia in inflammatory bowel disease.
Bokemeyer, B; Chopey, IV; Evstatiev, R; Gasche, C; Gutzwiller, FS; Iqbal, T; Khalif, IL; Marteau, P; Riopel, L; Stein, J, 2011
)
0.37
" Ferric carboxymaltose has a comparable safety profile to iron sucrose but offers the advantage of a much higher iron dosage at a time reducing the need for repeated applications and increasing patients' comfort."( Intravenous iron treatment in pregnancy: comparison of high-dose ferric carboxymaltose vs. iron sucrose.
Christoph, P; De Tejada, BM; Irion, O; Schuller, C; Studer, H; Surbek, D, 2012
)
0.38
"We assessed adverse event rates between dosing groups."( Comparison of the safety and efficacy of 3 iron sucrose iron maintenance regimens in children, adolescents, and young adults with CKD: a randomized controlled trial.
Goldstein, SL; Morris, D; Warady, BA, 2013
)
0.39
" Costs per 200/500/1,000 mg total dosage treatment cycle were CHF 101/210/420 for ferric carboxymaltose and CHF 144/375/721 for iron sucrose."( Budget impact of parenteral iron treatment of iron deficiency: methodological issues raised by using real-life data.
Braunhofer, P; Brock, E; Schneider, H; Troxler, J, 2014
)
0.4
" Bolus dosing was associated with an increase in infection-related events among both ferric gluconate and iron sucrose users."( Comparative Short-term Safety of Sodium Ferric Gluconate Versus Iron Sucrose in Hemodialysis Patients.
Brookhart, MA; Ellis, AR; Freburger, JK; Kshirsagar, AV; Wang, L; Winkelmayer, WC, 2016
)
0.43
" Maintaining hemodialysis patients within narrow hemoglobin targets, preventing cycling outside target, and reducing ESA dosing to prevent adverse outcomes requires considerable attention from caregivers."( Performance of a Predictive Model for Long-Term Hemoglobin Response to Darbepoetin and Iron Administration in a Large Cohort of Hemodialysis Patients.
Amato, C; Barbieri, C; Bellocchio, F; Bolzoni, E; Canaud, B; Cattinelli, I; Gatti, E; Macdougall, IC; Mari, F; Martin, JD; Stopper, A; Stuard, S, 2016
)
0.43
" IV iron can be given as large intermittent doses (loading therapy) or in smaller doses at frequent intervals (maintenance dosing regimen)."( Iron Treatment Strategies in Dialysis-Dependent CKD.
Coyne, DW; Daloul, R; Pandey, R, 2016
)
0.43
" Furthermore, iron isomaltoside has an advantage over iron sucrose in allowing higher cumulative dosing in fewer administrations."( A randomized trial of iron isomaltoside versus iron sucrose in patients with iron deficiency anemia.
Achebe, MM; Auerbach, M; Derman, R; Modiano, MR; Roman, E; Thomsen, LL, 2017
)
0.46
" Iron deficiency was modeled using dosing tables and retreatments were modeled based on a pooled retrospective analysis."( Intravenous iron treatments for iron deficiency anemia in inflammatory bowel disease: a budget impact analysis of iron isomaltoside 1000 (Monofer) in the UK.
Muduma, G; Pollock, RF, 2017
)
0.46
" The efficacy of MMF as an immunosuppressant and long-term safety in cats of this dosage regimen is unknown."(
Abrams, G; Adolfsson, E; Agarwal, PK; Akkan, AG; Al Alhareth, NS; Alves, VGL; Armentano, R; Bahroos, E; Baig, M; Baldridge, KK; Barman, S; Bartolucci, C; Basit, A; Bertoli, SV; Bian, L; Bigatti, G; Bobenko, AI; Boix, PP; Bokulic, T; Bolink, HJ; Borowiec, J; Bulski, W; Burciaga, J; Butt, NS; Cai, AL; Campos, AM; Cao, G; Cao, Y; Čapo, I; Caruso, ML; Chao, CT; Cheatum, CM; Chelminski, K; Chen, AJW; Chen, C; Chen, CH; Chen, D; Chen, G; Chen, H; Chen, LH; Chen, R; Chen, RX; Chen, X; Cherdtrakulkiat, R; Chirvony, VS; Cho, JG; Chu, K; Ciurlino, D; Coletta, S; Contaldo, G; Crispi, F; Cui, JF; D'Esposito, M; de Biase, S; Demir, B; Deng, W; Deng, Z; Di Pinto, F; Domenech-Ximenos, B; Dong, G; Drácz, L; Du, XJ; Duan, LJ; Duan, Y; Ekendahl, D; Fan, W; Fang, L; Feng, C; Followill, DS; Foreman, SC; Fortunato, G; Frew, R; Fu, M; Gaál, V; Ganzevoort, W; Gao, DM; Gao, X; Gao, ZW; Garcia-Alvarez, A; Garza, MS; Gauthier, L; Gazzaz, ZJ; Ge, RS; Geng, Y; Genovesi, S; Geoffroy, V; Georg, D; Gigli, GL; Gong, J; Gong, Q; Groeneveld, J; Guerra, V; Guo, Q; Guo, X; Güttinger, R; Guyo, U; Haldar, J; Han, DS; Han, S; Hao, W; Hayman, A; He, D; Heidari, A; Heller, S; Ho, CT; Ho, SL; Hong, SN; Hou, YJ; Hu, D; Hu, X; Hu, ZY; Huang, JW; Huang, KC; Huang, Q; Huang, T; Hwang, JK; Izewska, J; Jablonski, CL; Jameel, T; Jeong, HK; Ji, J; Jia, Z; Jiang, W; Jiang, Y; Kalumpha, M; Kang, JH; Kazantsev, P; Kazemier, BM; Kebede, B; Khan, SA; Kiss, J; Kohen, A; Kolbenheyer, E; Konai, MM; Koniarova, I; Kornblith, E; Krawetz, RJ; Kreouzis, T; Kry, SF; Laepple, T; Lalošević, D; Lan, Y; Lawung, R; Lechner, W; Lee, KH; Lee, YH; Leonard, C; Li, C; Li, CF; Li, CM; Li, F; Li, J; Li, L; Li, S; Li, X; Li, Y; Li, YB; Li, Z; Liang, C; Lin, J; Lin, XH; Ling, M; Link, TM; Liu, HH; Liu, J; Liu, M; Liu, W; Liu, YP; Lou, H; Lu, G; Lu, M; Lun, SM; Ma, Z; Mackensen, A; Majumdar, S; Martineau, C; Martínez-Pastor, JP; McQuaid, JR; Mehrabian, H; Meng, Y; Miao, T; Miljković, D; Mo, J; Mohamed, HSH; Mohtadi, M; Mol, BWJ; Moosavi, L; Mosdósi, B; Nabu, S; Nava, E; Ni, L; Novakovic-Agopian, T; Nyamunda, BC; Nyul, Z; Önal, B; Özen, D; Özyazgan, S; Pajkrt, E; Palazon, F; Park, HW; Patai, Á; Patai, ÁV; Patzke, GR; Payette, G; Pedoia, V; Peelen, MJCS; Pellitteri, G; Peng, J; Perea, RJ; Pérez-Del-Rey, D; Popović, DJ; Popović, JK; Popović, KJ; Posecion, L; Povall, J; Prachayasittikul, S; Prachayasittikul, V; Prat-González, S; Qi, B; Qu, B; Rakshit, S; Ravelli, ACJ; Ren, ZG; Rivera, SM; Salo, P; Samaddar, S; Samper, JLA; Samy El Gendy, NM; Schmitt, N; Sekerbayev, KS; Sepúlveda-Martínez, Á; Sessolo, M; Severi, S; Sha, Y; Shen, FF; Shen, X; Shen, Y; Singh, P; Sinthupoom, N; Siri, S; Sitges, M; Slovak, JE; Solymosi, N; Song, H; Song, J; Song, M; Spingler, B; Stewart, I; Su, BL; Su, JF; Suming, L; Sun, JX; Tantimavanich, S; Tashkandi, JM; Taurbayev, TI; Tedgren, AC; Tenhunen, M; Thwaites, DI; Tibrewala, R; Tomsejm, M; Triana, CA; Vakira, FM; Valdez, M; Valente, M; Valentini, AM; Van de Winckel, A; van der Lee, R; Varga, F; Varga, M; Villarino, NF; Villemur, R; Vinatha, SP; Vincenti, A; Voskamp, BJ; Wang, B; Wang, C; Wang, H; Wang, HT; Wang, J; Wang, M; Wang, N; Wang, NC; Wang, Q; Wang, S; Wang, X; Wang, Y; Wang, Z; Wen, N; Wesolowska, P; Willis, M; Wu, C; Wu, D; Wu, L; Wu, X; Wu, Z; Xia, JM; Xia, X; Xia, Y; Xiao, J; Xiao, Y; Xie, CL; Xie, LM; Xie, S; Xing, Z; Xu, C; Xu, J; Yan, D; Yan, K; Yang, S; Yang, X; Yang, XW; Ye, M; Yin, Z; Yoon, N; Yoon, Y; Yu, H; Yu, K; Yu, ZY; Zhang, B; Zhang, GY; Zhang, H; Zhang, J; Zhang, M; Zhang, Q; Zhang, S; Zhang, W; Zhang, X; Zhang, Y; Zhang, YW; Zhang, Z; Zhao, D; Zhao, F; Zhao, P; Zhao, W; Zhao, Z; Zheng, C; Zhi, D; Zhou, C; Zhou, FY; Zhu, D; Zhu, J; Zhu, Q; Zinyama, NP; Zou, M; Zou, Z, 2019
)
0.51
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
antineoplastic agentA substance that inhibits or prevents the proliferation of neoplasms.
[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 (1)

ClassDescription
glucaric acidA hexaric acid derived by oxidation of sugar such as glucose with nitric 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]

Pathways (2)

PathwayProteinsCompounds
Ascorbate and aldarate metabolism07
Biochemical pathways: part I0466

Research

Studies (937)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990239 (25.51)18.7374
1990's115 (12.27)18.2507
2000's261 (27.85)29.6817
2010's301 (32.12)24.3611
2020's21 (2.24)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 56.55

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index56.55 (24.57)
Research Supply Index7.07 (2.92)
Research Growth Index4.64 (4.65)
Search Engine Demand Index96.09 (26.88)
Search Engine Supply Index2.01 (0.95)

This Compound (56.55)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials167 (16.60%)5.53%
Reviews66 (6.56%)6.00%
Case Studies45 (4.47%)4.05%
Observational5 (0.50%)0.25%
Other723 (71.87%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]