Page last updated: 2024-12-05

3-o-methylglucose

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

Description

3-O-methylglucose is a glucose derivative with a methyl group attached to the 3-hydroxyl group. It is a non-metabolizable analog of glucose and is commonly used as a research tool in various biological studies. Synthesis: It can be synthesized using various chemical methods, often involving methylation of glucose. Effects: It is known to inhibit the activity of certain enzymes involved in glucose metabolism, such as hexokinase. Importance: It serves as a useful tool for studying glucose transport and metabolism. It can be used to assess glucose uptake and utilization by cells and tissues. It is also used to study the role of glucose in various cellular processes, such as insulin signaling and glycogen synthesis. Why it is studied: 3-O-methylglucose is studied to understand the role of glucose in biological systems, investigate the mechanisms of glucose transport, and develop novel therapeutic strategies for diseases related to glucose metabolism.'

3-O-Methylglucose: A non-metabolizable glucose analogue that is not phosphorylated by hexokinase. 3-O-Methylglucose is used as a marker to assess glucose transport by evaluating its uptake within various cells and organ systems. (J Neurochem 1993;60(4):1498-504) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

3-O-methyl-D-glucose : A D-aldohexose that is D-glucose in which the hydrogen of the hydroxy group at position 3 has been substituted by a methyl group. It is a non-metabolisable glucose analogue that is not phosphorylated by hexokinase and is used as a marker to assess glucose transport by evaluating its uptake within various cells and organ systems. [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 CID8973
CHEBI ID73918
SCHEMBL ID287865
MeSH IDM0028773

Synonyms (23)

Synonym
3-methyl-glucose
146-72-5
nsc-170119
d-glucose, 3-o-methyl-
methylglucose
3-o-methylglucose
3-o-methyl-d-glucose
glucose, 3-o-methyl-
96E16BFB-50E7-4E49-BB30-2B7CC2A7B717
(2r,3s,4r,5r)-2,4,5,6-tetrahydroxy-3-methoxyhexanal
3-methylglucose
o(3)-methyl-d-glucose
3-methyl-d-glucose
CHEBI:73918
unii-48du64i6o5
o-methyl-d-glucose
nsc 170119
48du64i6o5 ,
einecs 205-677-8
SCHEMBL287865
RMTFNDVZYPHUEF-XZBKPIIZSA-N
Q27144241
PD192677

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The lipophilic alloxan derivative, butylalloxan, was toxic also to non-transfected control cells."( Importance of the GLUT2 glucose transporter for pancreatic beta cell toxicity of alloxan.
Elsner, M; Guldbakke, B; Lenzen, S; Munday, R; Tiedge, M, 2002
)
0.31

Bioavailability

ExcerptReferenceRelevance
"To determine the effects of poorly absorbed solute on intestinal absorption, the urinary recovery of ingested lactulose, L-rhamnose, D-xylose, and 3-O-methyl-D-glucose was measured after simultaneous ingestion of various 'loads' of mannitol given in iso-osmolar solution."( The effect of poorly absorbed solute on intestinal absorption.
Catt, SD; Creamer, B; Heduan, E; Jenkins, AP; Menzies, IS; Segal, MB, 1990
)
0.28
" It eliminated hyperglycemia and restored the normal rate of absorption of AIB and 3-o-methyl glucose by the intestine."( Reversal by vanadate of the effect of diabetes on intestinal growth and transport.
Dobish, MP; Hajjar, JJ; Tomicic, TK, 1989
)
0.28
" The rates of 3OMG absorption immediately postoperative and 4 h later were 86 and 62% less than the absorption rate 6 d postoperative."( The effect of surgical bowel manipulation and anesthesia on intestinal glucose absorption in rats.
Kimura, RE; Uhing, MR, 1995
)
0.29
"We have previously shown that small oral doses of poorly absorbed solute can significantly reduce absorption of test sugars in normal volunteers."( The effect of ingested lactulose on absorption of L-rhamnose, D-xylose, and 3-O-methyl-D-glucose in subjects with ileostomies.
Creamer, B; Jenkins, AP; Menzies, IS; Nukajam, WS, 1994
)
0.29
" When we performed the same experiment on other sparrows in a situation in which intestinal glucose transporters were relatively unsaturated (200 mmol l(-1) mannitol replaced 3OMD-glucose in the gavage solution), the apparent rate of absorption was significantly reduced for [14C]l-glucose by 39% and for [3H]3OMD-glucose by 26%."( How the house sparrow Passer domesticus absorbs glucose.
Chang, MH; Karasov, WH, 2004
)
0.32
" In wattlebirds, we recorded higher bioavailability of L-glucose (96+/-3%) compared with D-glucose (57+/-2%), suggesting problems with the in vivo use of radiolabeled d-glucose."( Mechanism and rate of glucose absorption differ between an Australian honeyeater (Meliphagidae) and a lorikeet (Loriidae).
Fleming, PA; McWhorter, TJ; Napier, KR, 2008
)
0.35
" The relative absorption rate of 3-O-methyl-D-glucose calculated over the initial absorptive phase was not significantly different from that of D-glucose, indicating that the former provides reasonable estimates of glucose absorption rates in vivo."( Assessment of radiolabeled D-glucose and the nonmetabolizable analog 3-O-methyl-D-glucose as tools for in vivo absorption studies.
Green, AK; Karasov, WH; McWhorter, TJ,
)
0.13
" Relying on non-mediated transport of glucose may decrease its absorption rate at low glucose concentrations but may release small birds from the effects of glucose transport inhibitors."( Flavonoids have differential effects on glucose absorption in rats (Rattus norvegicus) and American robins (Turdis migratorius).
Green, AK; Karasov, WH; Skopec, MM, 2010
)
0.36

Dosage Studied

The insulin dose-response curves for 3-O-methylglucose transport did not differ between 1-month-old hybrid and control rats for either the soleus or epitrochlearis muscle.

ExcerptRelevanceReference
" This effect was rapid (t1/2 less than 5 min) and had a similar dose-response relationship as the effect on glucose transport."( Insulin can rapidly increase cell surface insulin binding capacity in rat adipocytes. A novel mechanism related to insulin sensitivity.
Eriksson, J; Lönnroth, P; Smith, U, 1992
)
0.28
" Chronic glucose exposure also reduced cell surface insulin binding by 30% via an apparent decrease in receptor affinity, and this effect was associated with a comparable rightward shift in the insulin-glucose transport dose-response curve."( Glucose and insulin chronically regulate insulin action via different mechanisms in BC3H1 myocytes. Effects on glucose transporter gene expression.
Garvey, WT; Maianu, L; Mayor, P, 1992
)
0.28
" In conclusion, C-peptide stimulates the rate of 3-0-methylglucose transport in in vitro incubated human skeletal muscle strips in a dose-response manner."( Effect of human C-peptide on glucose transport in in vitro incubated human skeletal muscle.
Galuska, D; Johansson, BL; Wallberg-Henriksson, H; Zierath, JR, 1991
)
0.28
" However the direct dose-response relationship between insulin and glucose transport has not yet been studied in human skeletal muscle."( Decreased insulin-stimulated 3-0-methylglucose transport in in vitro incubated muscle strips from type II diabetic subjects.
Andréasson, K; Galuska, D; Sonnenfeld, T; Thörne, A; Wallberg-Henriksson, H, 1991
)
0.28
" The dose-response effect of mannitol on the absorption of L-rhamnose was approximately exponential; doses of 5, 10, and 20 g mannitol reduced the average urinary excretion of L-rhamnose by 34."( The effect of poorly absorbed solute on intestinal absorption.
Catt, SD; Creamer, B; Heduan, E; Jenkins, AP; Menzies, IS; Segal, MB, 1990
)
0.28
" The dose-response curve for glucose transport was slightly shifted to the right in ovine adipocytes compared to rat adipocytes, indicating a small decrease in insulin sensitivity."( Mechanism of insulin resistance in the post receptor events in sheep: 3-O-methylglucose transport in ovine adipocytes.
Sasaki, S, 1990
)
0.51
" 45% and caused a marked rightward shift in the dose-response curve for insulin (EC50 103 +/- 34 mu units/ml)."( The interaction between the adenylate cyclase system and insulin-stimulated glucose transport. Evidence for the importance of both cyclic-AMP-dependent and -independent mechanisms.
Davies, JI; Lönnroth, I; Lönnroth, P; Smith, U, 1987
)
0.27
" In phosphate- and bicarbonate-free buffers the dose-response curve to insulin is shifted to the right, the effects of the hormone on hexose uptake, glucose metabolism, and inhibition of lipolysis being observed at much higher (nearly 2 orders of magnitude) concentrations of insulin."( Effect of depletion of phosphate and bicarbonate ions on insulin action in rat adipocytes.
Ron, A; Shechter, Y, 1986
)
0.27
" Analysis of the dose-response relationship with ALLFIT revealed that the maximal transport response to insulin was significantly decreased in both models of septic shock."( Basal and insulin-stimulated skeletal muscle sugar transport in endotoxic and bacteremic rats.
Sayeed, MM; Westfall, MV, 1988
)
0.27
" Dose-response studies of GS-Mal treatment of intact cells suggested that some functional carriers lack a reactive external sulfhydryl, which can be partially regenerated by pretreatment with excess cysteine."( Reaction of an exofacial sulfhydryl group on the erythrocyte hexose carrier with an impermeant maleimide. Relevance to the mechanism of hexose transport.
May, JM, 1988
)
0.27
", increased insulin sensitivity) manifested by a leftward shift in the 2-deoxyglucose dose-response curve."( Insulin induces progressive insulin resistance in cultured rat adipocytes. Sequential effects at receptor and multiple postreceptor sites.
Garvey, WT; Marshall, S; Olefsky, JM, 1986
)
0.27
" Although IGF-I (1-100 nM) and insulin (14 nM to 10 microM) also stimulated glycogen synthesis in fetal liver, the maximal effects of these hormones occurred at 2 h incubation, and the dose-response curves of IGF-I and insulin were not parallel to that of EGF."( Epidermal growth factor stimulates glycogen synthesis in fetal rat hepatocytes: comparison with the glycogenic effects of insulin-like growth factor I and insulin.
Freemark, M, 1986
)
0.27
" Insulin binding was increased by 30%, but no shift in the insulin dose-response curve for transport or metabolism occurred."( Regulation of glucose utilization in adipose cells and muscle after long-term experimental hyperinsulinemia in rats.
Cushman, SW; Hirshman, M; Horton, ED; Horton, ES; Mead, PM; Pofcher, E; Wardzala, LJ, 1985
)
0.27
" In purified B-cells, the intracellular concentration of glucose or 3-O-methyl-D-glucose equilibrates within 2 min with the extracellular levels, and, like in intact islets, the rate of glucose oxidation displays a sigmoidal dose-response curve for glucose."( Differences in glucose handling by pancreatic A- and B-cells.
Gorus, FK; Malaisse, WJ; Pipeleers, DG, 1984
)
0.27
" Dose-response curves for L-amino acids showed simple saturation."( Sodium-dependent sugar and amino acid transport in isolated goldfish intestinal epithelium: electrophysiological evidence against direct interactions at the carrier level.
Albus, H; Lippens, F; Siegenbeek van Heukelom, JS, 1983
)
0.27
" Consequently, the insulin dose-response curve of SSBG apparently shifted rightwards in KK mice."( Determination of overall insulin sensitivity in diabetic mice, KK.
Ikeda, H; Ishikawa, E; Iwatsuka, H; Taketomi, S, 1982
)
0.26
" The insulin dose-response curves for 3-O-methylglucose transport did not differ between 1-month-old hybrid and control rats for either the soleus or epitrochlearis muscle."( Development of decreased insulin-induced glucose transport in skeletal muscle of glucose-intolerant hybrids of diabetic GK rats.
Abdel-Halim, SM; Guenifi, A; Martin, IK; Nolte, LA; Ostenson, CG; Wallberg-Henriksson, H; Zierath, JR, 1995
)
0.56
" The dose-response curve for insulin-stimulated 3-O-methylglucose transport did not differ between the groups."( Insulin action on glucose transport in isolated skeletal muscle from patients with liver cirrhosis.
Eriksson, LS; Galuska, D; Johansson, U; Wallberg-Henriksson, H; Zierath, JR, 1994
)
0.54
" In HIT cells the abnormal glucose transport mechanism is associated with a marked shift to the left of the glucose-induced insulin release dose-response curve."( Inhibition of the high-affinity glucose transporter GLUT 1 affects the sensitivity to glucose in a hamster-derived pancreatic beta cell line (HIT).
Anello, M; Buscema, M; Caltabiano, V; Purrello, F; Rabuazzo, AM; Vigneri, R; Vinci, C, 1993
)
0.29
" Urine was collected for 5 h, test sugar content being subsequently measured by thin-layer chromatography for the dosing sugars."( Intestinal permeability and function in patients infected with human immunodeficiency virus. A comparison with coeliac disease.
Johnson, MA; Lee, CA; Lim, SG; Menzies, IS; Pounder, RE, 1993
)
0.29
" The blastocyst receptor was demonstrated to be functional, exhibiting the classic bell-shaped dose-response curves for GH stimulation of both 3-O-methyl glucose transport and protein synthesis."( Functional growth hormone (GH) receptors and GH are expressed by preimplantation mouse embryos: a role for GH in early embryogenesis?
Barnard, RT; Harvey, MB; Kaye, PL; Pantaleon, M; Waters, MJ; Whiteside, EJ, 1997
)
0.3
" Postmeal dosing had little impact, yet premeal dosing delayed and reduced 3-OMG absorption, with an AUC0-10 of 231±31 vs."( Selective sodium-dependent glucose transporter 1 inhibitors block glucose absorption and impair glucose-dependent insulinotropic peptide release.
Andrews, SM; Breed, SL; Chen, L; Dobbins, RL; Greenway, FL; Liu, Y; Smith, CD; Wald, JA; Walker, A, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
D-aldohexose derivativeAn aldohexose derivative that has D-configuration.
[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 (1,254)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990543 (43.30)18.7374
1990's468 (37.32)18.2507
2000's167 (13.32)29.6817
2010's69 (5.50)24.3611
2020's7 (0.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 17.62

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 Index17.62 (24.57)
Research Supply Index7.17 (2.92)
Research Growth Index4.21 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.62)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials25 (1.96%)5.53%
Reviews8 (0.63%)6.00%
Case Studies11 (0.86%)4.05%
Observational2 (0.16%)0.25%
Other1,231 (96.40%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]