Page last updated: 2024-12-06

mannose

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

Description

Mannose is a simple sugar (monosaccharide) that is a C-2 epimer of glucose. It is found in many plants and is a component of certain polysaccharides such as mannans. Mannose is a key component of glycoproteins and glycolipids in animal cells. Mannose is taken up by cells via specific mannose receptors and can be phosphorylated by mannose kinases. Mannose 6-phosphate is a key signal that directs lysosomal enzymes to lysosomes. Mannose is also a component of the glycocalyx, which is a layer of sugar molecules on the surface of cells that helps to protect cells and facilitate cell-cell interactions. Mannose is being studied for its potential therapeutic applications, such as in the treatment of cancer and infectious diseases. For example, some studies suggest that mannose may have anticancer effects by inhibiting tumor growth and metastasis. Mannose is also being investigated for its potential to enhance the immune system and to reduce inflammation.'

mannopyranose : The pyranose form of mannose. [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]

FloraRankFlora DefinitionFamilyFamily Definition
Ornusgenus[no description available]OleaceaeA plant family of the order Lamiales. The leaves are usually opposite and the flowers usually have four sepals, four petals, two stamens, and two fused carpels that form a single superior ovary.[MeSH]
FraxinusgenusA plant genus of the family OLEACEAE. Members contain secoiridoid glucosides.[MeSH]OleaceaeA plant family of the order Lamiales. The leaves are usually opposite and the flowers usually have four sepals, four petals, two stamens, and two fused carpels that form a single superior ovary.[MeSH]
Mannagenus[no description available]FabaceaeThe large family of plants characterized by pods. Some are edible and some cause LATHYRISM or FAVISM and other forms of poisoning. Other species yield useful materials like gums from ACACIA and various LECTINS like PHYTOHEMAGGLUTININS from PHASEOLUS. Many of them harbor NITROGEN FIXATION bacteria on their roots. Many but not all species of beans belong to this family.[MeSH]
Fraxinus ornusspecies[no description available]OleaceaeA plant family of the order Lamiales. The leaves are usually opposite and the flowers usually have four sepals, four petals, two stamens, and two fused carpels that form a single superior ovary.[MeSH]

Cross-References

ID SourceID
PubMed CID18950
CHEMBL ID469448
CHEBI ID4208
CHEBI ID37684
CHEBI ID16024
SCHEMBL ID38300
MeSH IDM0013001

Synonyms (64)

Synonym
MAN ,
smr000857125
MLS001332527
MLS001332528
530-26-7
CHEBI:4208 ,
mannopyranose
MANNOSE ,
seminose
d-mannopyranose ,
C00159
d-mannose ,
carubinose
d-(+)-mannose, from wood, >=99%
d-(+)-mannose, powder, bioreagent, suitable for cell culture
NCGC00166108-01
mannopyranoside
d-(+)-mannose, bioultra, >=99.5% (sum of enantiomers, hplc)
D50D2EC9-C1E4-4213-AFF7-F9C678AC92C5
AC-11148
(+)-mannose
BMSE000018
ai3-18442
(3s,4s,5s,6r)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol
CHEMBL469448
M0045
BMSE000874
BMSE000882
A829355
HMS2236J04
EPITOPE ID:152206
bdbm50448403
S5763
gtpl4650
SCHEMBL38300
alpha,beta-d-mannopyranose
d-mannopyranoside
d-man
AKOS025212856
mfcd00064122
d-(+)-mannose, for microbiology, >=99.0% (sum of enantiomers, hplc)
d-(+)-mannose, for microbiology, >=99%
mannose, united states pharmacopeia (usp) reference standard
d-(+)-mannose, p.a., 99.0%
d-(+)-mannose, synthetic, >=99%
(3s,4s,5s,6r)-6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol
DS-3390
CS-0238447
46032-76-2
2h-pyran-2,3,4,5-tetraol
(3s,4s,5s,6r)-6-(hydroxymethyl)tetrahydro-
d-mannose,(s)
Q335208
(3s,4s,5s,6r)-6-(hydroxymethyl)tetrahydro-2h-pyran-2,3,4,5-tetraol
d-mannose 1000 microg/ml in methanol
DTXSID501337491
EN300-19556
Z104474216
manno-hexose
(3s,4s,5r,6r)-6-(hydroxymethyl)tetrahydropyran-2,3,4,5-tetrol
dtxcid3020463
(3s,4s,5r,6r)-6-methyloltetrahydropyran-2,3,4,5-tetrol
chebi:37684
chebi:16024

Research Excerpts

Overview

D-mannose (D-m) is a glucose epimer found in natural products, especially fruits. d-Mannose is a promising nonantibiotic prophylaxis for recurrent urinary tract infection (rUTI)

ExcerptReferenceRelevance
"D-mannose (D-m) is a glucose epimer found in natural products, especially fruits. "( Oral D-mannose treatment suppresses experimental autoimmune encephalomyelitis via induction of regulatory T cells.
Boehm, A; Ciric, B; Hwang, D; Rostami, A; Zhang, GX, 2022
)
1.9
"d-Mannose is a promising nonantibiotic prophylaxis for recurrent urinary tract infection (rUTI). "( Recurrent Urinary Tract Infection Incidence Rates Decrease in Women With Cystitis Cystica After Treatment With d-Mannose: A Cohort Study.
Chiu, K; Lowder, JL; Mysorekar, IU; Sutcliffe, S; Zhang, F, 2022
)
1.65
"Mannose is a monosaccharide that is commonly found in sugar chains in the walls of fungi."( Mnt1, an α-(1 → 2)-mannosyltransferase responsible for the elongation of N-glycans and O-glycans in Aspergillus fumigatus.
Chihara, Y; Goto, M; Hira, D; Kadooka, C; Oka, T; Tanaka, Y, 2022
)
1.44
"D-mannose is a sugar part of normal human metabolism found within most diets."( D-mannose for preventing and treating urinary tract infections.
Cooper, TE; Howell, M; Jaure, A; Teixeira-Pinto, A; Teng, C; Wong, G, 2022
)
2
"D-mannose is a C-2 epimer of glucose, widely distributed in nature. "( D-Mannose ameliorates DNCB-induced atopic dermatitis in mice and TNF-α-induced inflammation in human keratinocytes via mTOR/NF-κB pathway.
Chang, B; Deng, F; Li, L; Li, Y; Liu, Y; Luo, J; Sun, L; Wang, D; Zeng, J; Zhai, Y; Zhang, J; Zhou, J; Zhu, Z, 2022
)
2.16
"Mannose is a naturally occurring sugar widely consumed in the daily diet; however, mechanistic insights into how mannose metabolism affects intestinal inflammation remain lacking. "( Mannose metabolism normalizes gut homeostasis by blocking the TNF-α-mediated proinflammatory circuit.
Cao, Q; Cheng, H; Guo, K; Hu, Z; Ke, Y; Lang, J; Mertens, RT; Pan, T; Shen, M; Xiao, P; Zhang, H; Zhang, X, 2023
)
3.8
"D-Mannose is a structural component in N-linked glycoproteins from viruses and mammals as well as in polysaccharides from fungi and bacteria. "( Glycosidic α-linked mannopyranose disaccharides: an NMR spectroscopy and molecular dynamics simulation study employing additive and Drude polarizable force fields.
Angles d'Ortoli, T; Aytenfisu, AH; MacKerell, AD; Ruda, A; Widmalm, G, 2023
)
1.63
"D-mannose is a natural C-2 epimer of D-glucose and is abundant in cranberries."( D-Mannose prevents bone loss under weightlessness.
Gu, R; Hu, M; Liu, H; Liu, X; Liu, Y; Song, D; Wang, F; Wu, L; Zhu, Y, 2023
)
2.19
"d-Mannose is a well-tolerated nutraceutical, but further research is needed to determine whether d-mannose in combination with VET has a significant, beneficial effect beyond VET alone in postmenopausal women with rUTIs."( d-Mannose for Recurrent Urinary Tract Infection Prevention in Postmenopausal Women Using Vaginal Estrogen: A Randomized Controlled Trial.
Chu, CM; Durkin, MJ; Ghetti, C; Jennings, Z; Lenger, SM; Lowder, JL; Sutcliffe, S; Wan, F, 2023
)
2.35
"Mannose is an oligosaccharide that specifically binds to the carbohydrate-recognition domain of C-type lectin; it has many physiological functions including reliving inflammation and regulating immune reaction."( Mannose facilitates Trichinella spiralis expulsion from the gut and alleviates inflammation of intestines and muscles in mice.
Cui, J; Dan Liu, R; Hao, HN; Li, YL; Long, SR; Lu, QQ; Wang, Z; Wang, ZQ, 2023
)
3.07
"Mannose/mannan is an essential component in many biomass resources, but Komagataeibacter xylinus uses mannose in an ineffective way, resulting in waste."( A recombinant strain of Komagataeibacter xylinus ATCC 23770 for production of bacterial cellulose from mannose-rich resources.
Cao, Z; Chen, L; Hong, FF; Li, C; Wu, G; Yang, F; Zhou, X, 2023
)
1.85
"D-mannose is expected to be a safe and effective treatment strategy for obesity."( D-mannose reduces adipogenesis by inhibiting the PI3K/AKT signaling pathway.
Gao, C; Li, X; Lin, H; Liu, Y; Wang, L; Zhao, J, 2023
)
2.19
"D-Mannose is an epimer of glucose at the C-2 position and exists in nature as a component of mannan. "( Recent studies on the biological production of D-mannose.
Mu, W; Wu, H; Zhang, W, 2019
)
1.49
"Mannose is a glucose-associated serum metabolite mainly released by the liver. "( Mannose is an insulin-regulated metabolite reflecting whole-body insulin sensitivity in man.
Andersson, K; Baboota, R; Baldi, S; Bokarewa, M; Brembeck, P; Campi, B; Ferrannini, E; Hedjazifar, S; Muscelli, E; Saba, A; Smith, U; Sterner, I; Wasen, C, 2020
)
3.44
"Mannose is a monosaccharide widely distributed in body fluids and tissues, especially in the nerve, skin, testicles, retina, liver and intestines. "( Mannose: Good player and assister in pharmacotherapy.
Cui, L; Huang, L; Wei, Z; Zhu, X, 2020
)
3.44
"D-mannose is a monosaccharide that is extracted from a larch rod."( [Use of D-mannose in the prevention of recurrent lower urinary tract infection in women].
Gyaurgiev, TA; Kuzmenko, AV; Kuzmenko, VV, 2020
)
1.52
"D-mannose is a monosaccharide approximately a hundred times less abundant than glucose in human blood. "( D-mannose suppresses macrophage IL-1β production.
Cardaci, S; Cuccovillo, I; Di Marco, S; Kajaste-Rudnitski, A; Mainini, F; Ricci, L; Ryan, KM; Scagliola, A; Sumpton, D; Torretta, S, 2020
)
2
"D-mannose is a C"( D-mannose ameliorates autoimmune phenotypes in mouse models of lupus.
Abboud, G; Li, W; Morel, L; Teng, X; Wang, H; Ye, S, 2021
)
1.9
"D-mannose is a type of sugar which is believed to inhibit bacterial adherence to uroepithelial cells, and is already being used by some women in an attempt to prevent RUTIs."( D-MannosE to prevent Recurrent urinary tract InfecTions (MERIT): protocol for a randomised controlled trial.
Allen, J; Butler, CC; Cook, J; Franssen, M; Glogowska, M; Hay, A; Hayward, G; Moore, M; Robinson, J; Thomas, N; Williams, N; Yang, Y, 2021
)
1.9
"Mannose receptor (MR) is a highly effective endocytic receptor. "( Mannosylated liposomes improve therapeutic effects of paclitaxel in colon cancer models.
Gao, T; Lei, Q; Song, X; Wang, N; Xia, Y; Xiong, M; Ye, T; You, X; Yu, L; Zhang, L, 2017
)
1.9
"Mannose is an important monosaccharide for protein glycosylation in mammals but is an inefficient cellular energy source. "( Mannose Alters Gut Microbiome, Prevents Diet-Induced Obesity, and Improves Host Metabolism.
Ayala, JE; Freeze, HH; Nayak, J; Peterson, SN; Scott, DA; Sharma, V; Smolin, J, 2018
)
3.37
"Mannose is a simple sugar with a complex life. "( Mannose metabolism: more than meets the eye.
Freeze, HH; Ichikawa, M; Sharma, V, 2014
)
3.29
"Paucimannose is a common mannosidic N-glycoepitope in invertebrates and plants but has only recently been detected in vertebrates."( Paucimannosidic glycoepitopes are functionally involved in proliferation of neural progenitor cells in the subventricular zone.
Dahmen, AC; Diestel, S; Fergen, MT; Laurini, C; Loke, I; Schmitz, B; Thaysen-Andersen, M, 2015
)
0.87
"β-Mannose is a major component of plant structural polysaccharides and eukaryotic N-glycans."( The GH130 Family of Mannoside Phosphorylases Contains Glycoside Hydrolases That Target β-1,2-Mannosidic Linkages in Candida Mannan.
Baslé, A; Cuskin, F; Davies, GJ; Day, AM; Gilbert, HJ; Ladevèze, S; Lowe, EC; Potocki-Véronèse, G, 2015
)
0.98
"D-mannose is a simple sugar; it seems able to hinder bacteria adhesion to the urothelium."( D-mannose: a promising support for acute urinary tract infections in women. A pilot study.
Benedetti Panici, P; Bracchi, C; Colagiovanni, V; Domenici, L; Giorgini, M; Monti, M; Muzii, L, 2016
)
1.71
"The mannose receptor (MR) is a transmembrane glycoprotein, postulated to be a link between innate and adaptive immunity. "( Schwann cells express the macrophage mannose receptor and MHC class II. Do they have a role in antigen presentation?
Alves, L; Baetas-da-Cruz, W; Barbosa, HS; Cavalcante, LA; Corte-Real, S; Pessolani, MC; Régnier-Vigouroux, A, 2009
)
1.18
"Mannose is an essential hexose that is required for glycoprotein synthesis. "( Physiological changes in circulating mannose levels in normal, glucose-intolerant, and diabetic subjects.
Ebinuma, H; Iida, KT; Kawakami, Y; Noguchi, Y; Okuda, Y; Saito, K; Shimano, H; Sone, H; Suzuki, H; Takahashi, A; Toyoshima, H; Ushizawa, K; Yamada, N; Yano, Y, 2003
)
2.03
"D-mannose is an essential monosaccharide constituent of glycoproteins and glycolipids. "( Hepatic glycogen breakdown is implicated in the maintenance of plasma mannose concentration.
Asano, N; Miwa, I; Mizutani, T; Nakajima, H; Taguchi, T; Yabuuchi, M; Yamashita, E, 2005
)
1.28
"The mannose receptor (MR) is a heavily glycosylated endocytic receptor that recognizes both mannosylated and sulfated ligands through its C-type lectin domains and cysteine-rich (CR) domain, respectively. "( Glycosylation influences the lectin activities of the macrophage mannose receptor.
Bakker, T; Brown, GD; Dwek, RA; Gordon, S; Harris, J; Martinez-Pomares, L; Rudd, PM; Su, Y; Tsang, C; Wormald, MR, 2005
)
1.12
"Mannose is an unusable carbon source for many plant species."( The use of the phosphomannose-isomerase/mannose selection system to recover transgenic apple plants.
Degenhardt, J; Montag, J; Poppe, A; Szankowski, I, 2006
)
1.37
"Mannose is a potentially useful tool in studies on hyaluronan-dependent cell functions, as demonstrated by reduced rates of keratinocyte proliferation and migration, functions known to depend on hyaluronan synthesis."( Mannose inhibits hyaluronan synthesis by down-regulation of the cellular pool of UDP-N-acetylhexosamines.
Auriola, S; Jauhiainen, M; Jokela, TA; Kauhanen, M; Tammi, MI; Tammi, RH; Tiihonen, R, 2008
)
2.51
"Mannose is an unusable carbon source for many plants. "( Mannose accommodation of Vigna angularis cells on solid agar medium involves its possible conversion to sucrose mediated by enhanced phosphomannose isomerase activity.
Inouhe, M; Kato, A, 2008
)
3.23
"Mannose is an acceptor, however, after treatment of microsomes with detergent."( The role of the membrane in the regulation of activity of microsomal glucose-6-phosphatase.
Edmondson, DE; Zakim, D, 1982
)
0.99
"Mannose 6-phosphate is a recognition marker used by many newly made acid hydrolases for their transport to lysosomes. "( Phosphorylation and subcellular location of alpha-L-fucosidase in lymphoid cells from patients with I-cell disease and pseudo-Hurler polydystrophy.
DiCioccio, RA; Miller, AL, 1993
)
1.73
"D(+)-Mannose is a D(+)-glucose epimer but in lenses incubated in 35.5 mM mannose, no mannitol (the sorbitol equivalent) was detected, while both lactate production and 31P profile appeared normal."( Manipulating rat lens glucose metabolism with exogenous substrates.
Cheng, FY; Cheng, HM; Pfleiderer, B; Tanaka, GH; Xiong, J, 1995
)
0.75
"Mannose is an aldohexose component of a number of glycoproteins in cellular membranes and blood plasma. "( Enzymatic determination of unbound D-mannose in serum.
Pitkänen, E; Pitkänen, O; Uotila, L, 1997
)
2.01
"As mannose is a sugar unique to the O7 subunit, this result suggested the presence of accumulated O7 LPS biosynthesis intermediates."( Surface expression of O-specific lipopolysaccharide in Escherichia coli requires the function of the TolA protein.
Gaspar, JA; Marolda, CL; Thomas, JA; Valvano, MA, 2000
)
0.82
"Mannose appeared to be a second major component of the alkali-soluble, water-soluble fraction."( Cell walls of Coccidioides immitis: neutral sugars of aqueous alkaline extract polymers.
Scheer, E; Wheat, R, 1977
)
0.98
"The mannose receptor (MR) is an opsonin-independent phagocytic receptor expressed on tissue macrophages."( Phagocytic chimeric receptors require both transmembrane and cytoplasmic domains from the mannose receptor.
Ezekowitz, RA; Kruskal, BA; Mathieu, CE; Sastry, K; Warner, AB, 1992
)
0.99
"D-Mannose is an epimer of D-glucose, differing in structure only in the axial, rather than equatorial, orientation of the hydroxyl group at the C-2 position of the pyranose ring."( A D-mannose transport system in renal brush-border membranes.
Mendelssohn, DC; Silverman, M, 1989
)
1.39

Effects

Mannose has been chosen as a sugar unit to test the viability of this strategy. High mannose has previously associated with insulin resistance and cardiovascular disease (CVD) D-mannose has great value in the treatment of chronic diseases. Mannose has anticancer activity that inhibits cell proliferation and enhances the efficacy of chemotherapy.

ExcerptReferenceRelevance
"High mannose has previously associated with insulin resistance and cardiovascular disease (CVD). "( Mannose as a biomarker of coronary artery disease: Angiographic evidence and clinical significance.
Andreini, D; Burgmaier, M; Campi, B; Ferrannini, E; Ferrannini, G; Gorini, M; Maggioni, AP; Magnoni, M; Marx, N; Maseri, A; Milzi, A; Saba, A, 2022
)
2.68
"D-Mannose has great value in the treatment of chronic diseases. "( Characterization of a Novel Mannose Isomerase from Stenotrophomonas rhizophila and Identification of Its Possible Catalytic Residues.
Chen, Q; Guang, C; Huang, Z; Mu, W; Wu, Y; Zhang, W, 2022
)
1.74
"Mannose has anticancer activity that inhibits cell proliferation and enhances the efficacy of chemotherapy. "( Metabolic clogging of mannose triggers dNTP loss and genomic instability in human cancer cells.
Dohmae, N; Freeze, HH; Harada, Y; Higashiyama, S; Hiratsuka, T; Hirayama, A; Ikeda, S; Imagawa, Y; Maeda, K; Miyoshi, E; Mizote, Y; Murai, J; Nishida, M; Ohkawa, Y; Suzuki, T; Tahara, H; Taniguchi, N; Udono, H; Ueda, A, 2023
)
2.67
"Mannose has been reported as a novel drug to kill cancer cells. "( Sharp pH-responsive mannose prodrug polypeptide nanoparticles encapsulating a photosensitizer for enhanced near infrared imaging-guided photodynamic therapy.
Cheng, Q; Li, T; Ruan, Z; Tian, Y; Yan, L; Yuan, P, 2019
)
2.28
"Mannose has good, bad or ugly outcomes depending on its steady state levels and metabolic flux."( Mannose metabolism: more than meets the eye.
Freeze, HH; Ichikawa, M; Sharma, V, 2014
)
2.57
"Mannose has been reported to prevent acute lung injury (ALI), and mannose receptor (MR) has been demonstrated to have a role. "( Mannose prevents acute lung injury through mannose receptor pathway and contributes to regulate PPARγ and TGF-β1 level.
Li, HQ; Lu, GH; Shen, YH; Wang, YH; Xu, XL; Zhang, P; Zhou, JY, 2015
)
3.3
"Mannose has prebiotic effect; the ability of mannose to induce expression of pro- and anti-inflammatory cytokines gives evidence of immunostimulating properties of the monosaccharide."( [Prebiotic properties of mannose and its effect on specific resistance].
Baturo, AP; Cheremushkina, IV; Glushchenko, AS; Korneeva, OS; Mikhaĭlova, NA; Romanenko, ÉE; Zlygostev, SA,
)
1.88
"Mannose has been chosen as a sugar unit to test the viability of this strategy."( Glycodendritic structures based on Boltorn hyperbranched polymers and their interactions with Lens culinaris lectin.
Arce, E; Bernad, A; Castro, RG; Díaz, V; Nieto, PM; Rojo, J,
)
0.85
"D-mannose has been found to inhibit the process in the dose-dependent way causing the full blockage at 10 mM concentration."( [The effect of metabolic inhibitors on resistance of mannose-specific contacts of Escherichia coli K12 and human neutrophils].
Cherenkevich, SN; Fomichev, AIu; Timoshenko, AV,
)
0.94
"Mannose-2-14C has been fermented by Leuconostoc mesenteroides, CO2 ethanol and D-lactic acid were formed in a molar ratio of 1:1:1. "( [Fermentative degradation of 2-14C-mannose with Leuconostoc mesenteroides (author's transl)].
Dahmen, J; Ziegler, E, 1975
)
1.97
"D-Mannose derivatives have been synthesised which are crosslinked through their C-4 hydroxyls to propyl-2-amine. "( A new class of sugar analogues for use in the investigation of sugar transport.
Holman, GD; Midgley, PJ; Parkar, BA, 1985
)
0.99

Actions

D-mannose plays an important role in glucose metabolism. Whether it is beneficial to prevention and treatment of periodontitis is still unknown. Mannose seems to suppress wounding-induced inflammation in skin by attenuating hyaluronan synthesis.

ExcerptReferenceRelevance
"D-Mannose isomerase can catalyze the bioconversion of D-fructose to D-mannose."( Characterization of a Novel Mannose Isomerase from Stenotrophomonas rhizophila and Identification of Its Possible Catalytic Residues.
Chen, Q; Guang, C; Huang, Z; Mu, W; Wu, Y; Zhang, W, 2022
)
1.57
"D-mannose plays an important role in glucose metabolism; whether it is beneficial to prevention and treatment of periodontitis and the regulation of oral and intestinal microbiota changes is still unknown."( D-mannose alleviated alveolar bone loss in mice with experimental periodontitis via regulating the anti-inflammatory effect of amino acids.
Guo, L; Han, N; Liu, Y; Luo, Z; Xu, J; Yang, H, 2023
)
2.19
"Mannose thus seems to suppress wounding-induced inflammation in skin by attenuating hyaluronan synthesis."( Mannose reduces hyaluronan and leukocytes in wound granulation tissue and inhibits migration and hyaluronan-dependent monocyte binding.
Jokela, TA; Kärnä, R; Kössi, J; Kuokkanen, J; Laato, M; Pasonen-Seppänen, S; Rilla, K; Tammi, MI; Tammi, RH,
)
2.3
"Mannose trimming plays an important role by forming specific N-glycans that permit the recognition and sorting of terminally misfolded conformers for ERAD (ER-associated degradation)."( EDEM1 accelerates the trimming of alpha1,2-linked mannose on the C branch of N-glycans.
Herscovics, A; Hosokawa, N; Kamiya, Y; Kato, K; Nagata, K; Sleno, B; Tremblay, LO; Wada, I, 2010
)
1.34
"D-Mannose may cause growth inhibition of bloodstream trypanosomes through an extremely high concentration of D-mannose 6-phosphate in the glycosomes."( Rapid uptake and phosphorylation of D-mannose, and limited D-mannose 6-phosphate isomerization in the glycolytic pathway of bloodstream forms of Trypanosoma brucei gambiense.
Fukuma, T; Hara, T; Kanbara, H; Nakao, M, 1997
)
1.13
"Mannose did not inhibit the re-elevation of neural folds which had been caused to collapse by exposure to medium containing low calcium."( The effects of mannose on rat embryos grown in vitro.
Beck, F; Clarke, CA; Moore, DC; Stanisstreet, M, 1987
)
1.35

Treatment

Mannose-BSA, a weak agonist of the MR containing a lower ratio of attached sugar compared with pure polysaccharides, before the addition of mannan inhibited COX-2 expression. Pre-treatment with mannose attenuated pulmonary edema and protein exudation in a dose-dependent manner.

ExcerptReferenceRelevance
"Mannose treatment of PCa cells induced changes in mitochondrial morphology, caused dysregulated expression of the fission protein, such as fission, mitochondrial 1 (FIS1), and enhanced the expression of proapoptotic factors, such as BCL2-associated X (Bax) and BCL2-antagonist/killer 1 (Bak)."( Mannose inhibits the growth of prostate cancer through a mitochondrial mechanism.
Cai, SH; Cai, ZD; Chen, QB; Deng, YL; Feng, YF; Han, ZD; Liu, R; Zhong, WD; Zhu, JG,
)
2.3
"Mannose treatment attenuates intestinal barrier damage in two mouse colitis models, dextran sodium sulfate (DSS)-induced colitis and spontaneous colitis in IL-10-deficient mice."( Mannose ameliorates experimental colitis by protecting intestinal barrier integrity.
Chen, K; Chen, Z; Dong, L; He, J; Jiang, H; Li, D; Liu, Y; Lu, X; Wang, J; Wang, Q; Wang, XY; Wang, Y; Xie, J; Zhang, L; Zhou, J; Zou, X; Zuo, D, 2022
)
2.89
"mannose pretreatment significantly and dose-dependently prolonged pDNA-IL-10 pain suppressive effects, reduced spinal IL-1β and enhanced spinal and dorsal root ganglia IL-10 immunoreactivity."( Improvement of spinal non-viral IL-10 gene delivery by D-mannose as a transgene adjuvant to control chronic neuropathic pain.
Alberti, LA; Bowman, BN; Dengler, EC; Kerwin, AA; Limanovich, E; Milligan, ED; Moezzi, DR; Wallace, JA; Wilkerson, JL, 2014
)
1.37
"Mannose pre-treatment reduced enhanced killing by combination treatments, accompanied by reduced DR5 levels."( 2-deoxyglucose sensitizes melanoma cells to TRAIL-induced apoptosis which is reduced by mannose.
Nickoloff, BJ; Qin, JZ; Xin, H, 2010
)
1.3
"Mannose pretreatment of RK13 host cells decreased their infection by E."( Glycosylation of the major polar tube protein of Encephalitozoon hellem, a microsporidian parasite that infects humans.
Cali, A; Orr, G; Takvorian, PM; Weiss, LM; Xu, Y, 2004
)
1.04
"Mannose treatment of asparagus (Asparagus officinalis) cells and spinach (Spinacia oleracea) protoplasts results in the inhibition of photosynthesis."( Observations on the phosphate status and intracellular pH of intact cells, protoplasts and chloroplasts from photosynthetic tissue using phosphorus-31 nuclear magnetic resonance.
Foyer, C; Mann, B; Spencer, C; Walker, D, 1982
)
0.99
"Oral mannose treatment at a dose of 0.17 g/kg body weight 6 times/d was followed by a clinical improvement and normalization of blood glucose, aminotransferases, and coagulation factor levels."( Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose.
Beaune, G; Castelnau, P; Cuer, M; de Lonlay, P; Durand, G; Kretz, M; Saudubray, JM; Seta, N; Vuillaumier-Barrot, S, 1999
)
1
"Mannose-treated embryos also showed delayed development according to morphological criteria, and a range of abnormalities including abnormalities of the neural tube."( The effects of mannose on rat embryos grown in vitro.
Beck, F; Clarke, CA; Moore, DC; Stanisstreet, M, 1987
)
1.35
"Treatment with mannose-BSA, a weak agonist of the MR containing a lower ratio of attached sugar compared with pure polysaccharides, before the addition of mannan inhibited COX-2 expression, whereas this was not observed when agonists other than mannan and zymosan were used."( Mannose-containing molecular patterns are strong inducers of cyclooxygenase-2 expression and prostaglandin E2 production in human macrophages.
Alonso, S; Barbolla, L; Crespo, MS; Fernández, N; Renedo, M; Valera, I; Vigo, AG, 2005
)
2.11
"Pre-treatment with mannose attenuated pulmonary edema and protein exudation in a dose-dependent manner, the maximal effect was similar to or greater than that of DXM. "( Mannose prevents lipopolysaccharide-induced acute lung injury in rats.
Chen, YY; Jiang, JJ; Shen, YH; Xie, QM; Xu, XL; Yao, HY; Zhou, JY, 2008
)
2.12

Toxicity

2-Deoxyglucose is as toxic as mannose for honeybees and is toxic also for the other insects studied. Since no damage to the skin at the injection site was caused by the liposomes, they may be suitable for use as a safe adjuvant in vaccines inducing a CTL response against HIV.

ExcerptReferenceRelevance
" In this article, the toxic effect of CsA on pancreatic islet cells and the preventive effect of K-MAP on CsA-associated islet cell toxicity were investigated."( Modulation of prostaglandin metabolism by K-MAP and prevention of toxic effect of cyclosporin on pancreatic islet cells.
Babazono, T; Fuchinoue, S; Fujikawa, H; Fujita, S; Hayashi, T; Honda, H; Kawai, T; Nakagawa, Y; Nakajima, I; Teraoka, S, 1989
)
0.28
" 2-Deoxyglucose is as toxic as mannose for honeybees and is toxic also for the other insects studied, which supports the conclusion that the mechanism of mannose toxicity involves large accumulation of a hexosephosphate."( Mechanism of mannose toxicity.
de la Fuente, M; Peñas, PF; Sols, A, 1986
)
0.93
" The blocking of NC-mediated cytotoxicity was not due to a direct toxic action of the sugars on the effector cells."( Natural cytotoxic cells against solid tumors in mice: blocking of cytotoxicity by D-mannose.
Dien, P; Lattime, EC; Stutman, O; Wisun, RE, 1980
)
0.49
" It is concluded that while ricin and abrin share a common mechanism of action ricin is slightly less toxic than abrin."( Examination of the toxicity of several protein toxins of plant origin using bovine pulmonary endothelial cells.
Griffiths, GD; Lindsay, CD; Upshall, DG, 1994
)
0.29
" Since no damage to the skin at the injection site was caused by the liposomes, and since the oligomannose-coated liposomes consist of innocuous materials ubiquitously distributed throughout the human body, they may be highly suitable for use as a safe adjuvant in vaccines inducing a CTL response against HIV."( Liposome oligomannose-coated with neoglycolipid, a new candidate for a safe adjuvant for induction of CD8+ cytotoxic T lymphocytes.
Fukasawa, M; Hatanaka, M; Mizuochi, T; Nakata, M; Sakakibara, R; Shikata, K; Shimizu, Y; Yamamoto, N, 1998
)
0.88
"Microglial cells, like macrophages, are very sensitive to ricin, a galactose-specific toxic lectin belonging to the family of ribosome-inactivating proteins."( Ricin toxicity to microglial and monocytic cells.
Battelli, MG; Buonamici, L; Contestabile, A; Monti, B; Musiani, S; Sparapani, M; Stirpe, F, 2001
)
0.31
" Bimosiamose was safe and well-tolerated."( Physiochemical properties, safety and pharmacokinetics of bimosiamose disodium after intravenous administration.
Jilma, B; Meyer, M; Wolff, G; Zahlten, R, 2005
)
0.33
" Nanoparticle functionalization with di-mannose (specifically carboxymethyl-α-D-mannopyranosyl-(1,2)-D-mannopyranoside), galactose (specifically carboxymethyl-β-galactoside), or glycolic acid induced no adverse effects after administration based on histopathological evaluation of liver, kidneys, and lungs."( Safety and biocompatibility of carbohydrate-functionalized polyanhydride nanoparticles.
Boggiatto, PM; Goodman, JT; Hostetter, JM; Narasimhan, B; Pohl, NL; Roychoudhury, R; Vela-Ramirez, JE; Wannemuehler, MJ, 2015
)
0.68
"Ag-NPs coated with galactose and mannose were considerably less toxic to neuronal-like cells and hepatocytes compared to particles functionalized by glucose, ethylene glycol or citrate."( Carbohydrate functionalization of silver nanoparticles modulates cytotoxicity and cellular uptake.
Haase, A; Kennedy, DC; Lai, CH; Luch, A; Müller, L; Orts-Gil, G; Seeberger, PH, 2014
)
0.68
" Diarrhea was the most frequent side-effect in both groups."( [Efficacy and safety of D-mannose (2 g), 24h prolonged release, associated with Proanthocyanidin (PAC), versus isolate PAC, in the management of a series of women with recurrent urinary infections.]
Esteban-Fuertes, M; Gómez-Rodríguez, A; Luján-Galán, M; Méndez-Rubio, S; Rituman, G; Salinas-Casado, J; Vírseda-Chamorro, M, 2018
)
0.78

Pharmacokinetics

High mannose glycans can impact pharmacokinetic (PK) profile. We performed a retrospective evaluation of 21 monoclonal antibody biosimilar programs.

ExcerptReferenceRelevance
" Pharmacokinetic analysis revealed that their uptake rates were sufficiently large for selective drug targeting."( Synthesis and pharmacokinetics of a new liver-specific carrier, glycosylated carboxymethyl-dextran, and its application to drug targeting.
Fujita, T; Hashida, M; Kamijo, A; Nishikawa, M; Sezaki, H; Takakura, Y, 1993
)
0.29
" The outflow curves of each 111In-Man-BSA at three concentrations were simultaneously fitted to a pharmacokinetic model including a binding to the cell surface and an internalization, by using a nonlinear regression program MULTI(RUNGE)."( Pharmacokinetic evaluation of mannosylated bovine serum albumin as a liver cell-specific carrier: quantitative comparison with other hepatotropic ligands.
Hasegawa, S; Hashida, M; Nishikawa, M; Ogawara, K; Takakura, Y, 1999
)
0.3
" These results could be of great significance for PNA drug development, as they should allow modulation and fine-tuning of the pharmacokinetic profile of a drug lead."( Modulation of the pharmacokinetic properties of PNA: preparation of galactosyl, mannosyl, fucosyl, N-acetylgalactosaminyl, and N-acetylglucosaminyl derivatives of aminoethylglycine peptide nucleic acid monomers and their incorporation into PNA oligomers.
Dahl, O; Dolle, F; Hamzavi, R; Nielsen, PE; Tavitian, B,
)
0.13
" Haematological changes, tissue distribution and pharmacokinetic studies of free, liposomal and mannosylated liposomal drug were performed following a bolus intravenous injection in Sprague-Dawley rats."( Stavudine-loaded mannosylated liposomes: in-vitro anti-HIV-I activity, tissue distribution and pharmacokinetics.
Agashe, HB; Agrawal, GP; Asthana, A; Garg, M; Jain, NK, 2006
)
0.33
" The therapeutic IgGs were affinity purified from serum samples from human pharmacokinetic studies, and changes to the glycan profile over time were determined by peptide mapping employing high-resolution mass spectrometry."( High-mannose glycans on the Fc region of therapeutic IgG antibodies increase serum clearance in humans.
Bondarenko, PV; Flynn, GC; Goetze, AM; Lee, E; Liu, YD; Shah, B; Zhang, Z, 2011
)
0.88
"The role of Fc glycans on clearance of IgG molecule has been examined by various groups in experiments where specific glycans have been enriched or the entire spectrum of glycans was studied after administration in pre-clinical or clinical pharmacokinetic (PK) studies."( Increased serum clearance of oligomannose species present on a human IgG1 molecule.
Acquah, A; Alessandri, L; Correia, I; Fujimori, T; Leblond, D; Ouellette, D; Radziejewski, C; Rieser, M; Saltarelli, M,
)
0.41
" When compared with historical data, the antibodies bearing the high mannose glycoform exhibited faster clearance rate compared with antibodies bearing the fucosylated complex glycoform, while the pharmacokinetic properties of antibodies with Man8/9 and Man5 glycoforms appeared similar."( Production, characterization, and pharmacokinetic properties of antibodies with N-linked mannose-5 glycans.
Bayer, R; Brown, D; Chung, S; Lutman, J; Reed, C; Stefanich, E; Stephan, JP; Wong, A; Yu, M,
)
0.59
" With a sensitive method designed to measure HM pairing, we followed the levels of symmetrically and asymmetrically paired HM on antibodies in human pharmacokinetic serum samples to determine the impact of Fc HM glycan pairing on therapeutic human IgG clearance in humans."( Effect of high mannose glycan pairing on IgG antibody clearance.
Flynn, GC; Liu, YD, 2016
)
0.79
" Ciprofloxacin dosed in identical fashion displayed rapid clearance with a half-life of approximately 30 min."( Macrophage-targeted drugamers with enzyme-cleavable linkers deliver high intracellular drug dosing and sustained drug pharmacokinetics against alveolar pulmonary infections.
Chen, J; Convertine, AJ; Lee, B; Ratner, DM; Skerrett, SJ; Srinivasan, S; Stayton, PS; Su, FY; West, TE, 2018
)
0.48
" Furthermore, pharmacokinetic studies revealed that these MDM esters may be worth considering as potent candidates for oral and topical administration."( Novel mannopyranoside esters as sterol 14α-demethylase inhibitors: Synthesis, PASS predication, molecular docking, and pharmacokinetic studies.
Alam, MS; Chakraborty, P; Hanee, U; Islam, MM; Matin, MM, 2020
)
0.56
"Good pharmacokinetic (PK) behavior is a key prerequisite for sufficient efficacy of therapeutic monoclonal antibodies (mAbs)."( Glycoform-resolved pharmacokinetic studies in a rat model employing glycoengineered variants of a therapeutic monoclonal antibody.
Falck, D; Jany, C; Koeleman, CAM; Lechmann, M; Malik, S; Reusch, D; Thomann, M; Wuhrer, M,
)
0.13
" Given the well-established conclusion that high mannose glycans can impact pharmacokinetic (PK) profile, we performed a retrospective evaluation of 21 monoclonal antibody biosimilar programs (those licensed before April 2022), their levels of glycans, and the methods used to study them."( The Mannose in the Mirror: A Reflection on the Pharmacokinetic Impact of High Mannose Glycans of Monoclonal Antibodies in Biosimilar Development.
Ausin, C; Brahme, N; Lacana, E; Ricci, S; Schultz-DePalo, M; Welch, J, 2023
)
1.72

Compound-Compound Interactions

A method involving the use of doxorubicin-loaded polyethylene-glycol-modified liposomes and transfection using mannose-modified bubble lipoplexes in combination with ultrasound irradiation may be a promising approach to cancer treatment. It could not only suppress early-stage tumor growth but also enhance transfections efficacy in antigen-presenting cells.

ExcerptReferenceRelevance
" Preparative size-exclusion chromatography (SEC) and analytical SEC combined with three detectors were used to detect the TM1 and TM2 samples, confirming that the proteins were bonded to the polysaccharides."( Characterization of polysaccharide-protein complexes by size-exclusion chromatography combined with three detectors.
Tao, Y; Zhang, L, 2008
)
0.35
"To understand the cytochemical properties of epididymal epithelial cells, the characteristics of glycoconjugates in the mouse epididymis were examined using the technique of lectin histochemistry combined with immunohistochemistry."( Cell- and region-specific expression of sugar chains in the mouse epididymal epithelium using lectin histochemistry combined with immunohistochemistry.
Fukui, T; Sawaguchi, A; Tajiri, S; Yoshinaga, K, 2012
)
0.38
"A method involving the use of doxorubicin-loaded polyethylene-glycol-modified liposomes and transfection using mannose-modified bubble lipoplexes in combination with ultrasound irradiation may be a promising approach to cancer treatment; it could not only suppress early-stage tumor growth but also enhance transfection efficacy in antigen-presenting cells, thus enhancing the therapeutic potential of a DNA vaccine."( Enhancement of the anti-tumor effect of DNA vaccination using an ultrasound-responsive mannose-modified gene carrier in combination with doxorubicin-encapsulated PEGylated liposomes.
Hashida, M; Higuchi, Y; Kawakami, S; Kono, Y; Maruyama, K; Un, K; Yamashita, F; Yoshida, M, 2014
)
0.84
"To evaluate the efficacy of mannatide combined with sodium cantharidate vitamin B6 in the treatment of malignant pleural effusions."( Efficacy of mannatide combined with sodium cantharidate vitamin B6 in the treatment of malignant pleural effusions.
Song, J; Wang, LZ; Zhang, HJ, 2015
)
0.42
" Injection into the thorax using mannatide combined with sodium cantharidate vitamin B6 was performed for 37 patients in the experimental group and mannatide combined with cisplatin for 32 patients in the control group."( Efficacy of mannatide combined with sodium cantharidate vitamin B6 in the treatment of malignant pleural effusions.
Song, J; Wang, LZ; Zhang, HJ, 2015
)
0.42
"Regimen of mannatide combined with sodium cantharidate vitamin B6 had better improvement in quality-of-life and symptom relief, with a lower side-effect incidence in treatment of malignant pleural effusions."( Efficacy of mannatide combined with sodium cantharidate vitamin B6 in the treatment of malignant pleural effusions.
Song, J; Wang, LZ; Zhang, HJ, 2015
)
0.42
"The results of the study demonstrated the high efficacy and safety of complex therapy with Ecofomural containing fosfomycin and lactulose, in combination with long-term enrichment of the diet with D-mannose (Ecocystin) b in order to prolong the inter-relapse period of uncomplicated lower urinary tract infection."( [Efficacy of combined antibacterial-prebiotic therapy in combination with D-mannose in women with uncomplicated lower urinary tract infection].
Gyaurgiev, TA; Kuzmenko, AV; Kuzmenko, VV, 2019
)
0.93

Bioavailability

Study evaluated mannose-anchored thiolated chitosan (MTC) based nanocarriers for enhanced permeability, improved oral bioavailability and anti-parasitic potential of amphotericin B.

ExcerptReferenceRelevance
" Systemic bioavailability after inhalation is low."( Tolerability and pharmacokinetics of inhaled bimosiamose disodium in healthy males.
Aydt, E; Beeh, KM; Beier, J; Beyer, D; Jilma, B; Meyer, M; Wolff, G; Zahlten, R, 2007
)
0.34
" The bioavailability of the mannose residues as specific recognition sites on the nanoparticle surface could be demonstrated by a modified enzyme-linked lectin assay (ELLA) using biotin-labeled lectins which interact specifically with alpha-D-mannopyrannoside derivatives."( Polyester nanoparticles presenting mannose residues: toward the development of new vaccine delivery systems combining biodegradability and targeting properties.
Auzély-Velty, R; Delair, T; Freichels, H; Imberty, A; Jérôme, C; Putaux, JL; Rieger, J, 2009
)
0.92
" Structure-activity relationships (SAR) and structure-property relationship (SPR) studies have resulted in the rapid development of orally bioavailable FimH antagonists with promising therapeutic potential for UTI and CD."( Mannose-derived FimH antagonists: a promising anti-virulence therapeutic strategy for urinary tract infections and Crohn's disease.
Cusumano, ZT; Janetka, JW; Mydock-McGrane, LK, 2016
)
1.88
"The aim of this study was to evaluate mannose-anchored thiolated chitosan (MTC) based nanocarriers (NCs) for enhanced permeability, improved oral bioavailability and anti-parasitic potential of amphotericin B (AmB)."( Design of mannosylated oral amphotericin B nanoformulation: efficacy and safety in visceral leishmaniasis.
Akhtar, S; Gendelman, HE; Nadhman, A; Rehman, AU; Saljoughian, N; Sarwar, HS; Satoskar, AR; Shahnaz, G; Sohail, MF; Yasinzai, M, 2018
)
0.75
"Mannosylated polymeric nanoparticles (NPs) enable improvement of brain bioavailability and reduction of dosing due to efficient drug delivery at the target site."( Targeted delivery of mannosylated-PLGA nanoparticles of antiretroviral drug to brain.
Parikh, RH; Patel, BK; Patel, N, 2018
)
0.48
" Their bioavailability for intracellular bacterial pools, however, is limited by poor membrane permeability and rapid elimination."( Polymer-augmented liposomes enhancing antibiotic delivery against intracellular infections.
Chen, J; Convertine, AJ; Kelly, AM; Ratner, DM; Skerrett, SJ; Son, HN; Stayton, PS; Su, FY; West, TE, 2018
)
0.48
" However, their high polarity makes them poorly absorbed by the body and their penetration inside the cell is even more difficult without a proper transporter."( Synthesis of 2-Acetamido-1,3,4-Tri-O-Acetyl-2-Deoxy-D-Mannopyranose -6-Phosphate Prodrugs as Potential Therapeutic Agents.
Morewood, J; Pertusati, F, 2022
)
0.72
" However, its hydrophobicity results in low bioavailability that limits application."( Glycyrrhetinic acid proliposomes mediated by mannosylated ligand: Preparation, physicochemical characterization, environmental stability and bioactivity evaluation.
Cen, K; Chen, J; Cheng, Y; Li, C; Liao, Y; Lin, Y; Liu, F; Wu, M; Xu, J; Zhou, X, 2022
)
0.72
" The functionalized nanoparticles could overcome the limitation of poor drug bioavailability and showed a high loading capacity of (45 %) with a controlled release of about (74."( Multifunctional nanoparticles based on marine polysaccharides for apremilast delivery to inflammatory macrophages: Preparation, targeting ability, and uptake mechanism.
Abdalla, M; Chi, Z; Hamouda, HI; Liu, C; Shabana, S; Sharaf, M, 2022
)
0.72
" However, the poor bioavailability and potential toxicity of this combo strategy remain a challenge."( Targeted co-delivery of resiquimod and a SIRPα variant by liposomes to activate macrophage immune responses for tumor immunotherapy.
Guo, W; Jia, D; Li, G; Li, J; Liu, R; Lu, X; Lu, Y; Lv, M; Wang, F; Wang, R; Wei, J; Yuan, F; Zhu, W, 2023
)
0.91

Dosage Studied

D-mannose is a competitive inhibitor of Con A binding to its receptor. The effect of this on pharmacokinetic area under the curve was calculated and shown to be relatively minor for three of the four molecules studied.

ExcerptRelevanceReference
" There was a dose-response relationship between the amount of drug administered to the rats and 14C labeling of the membrane pool of factor X carboxylase substrates."( Early processing of prothrombin and factor X by the vitamin K-dependent carboxylase.
Martin, LF; Wallin, R, 1988
)
0.27
" We report a dosage dependent stimulation of both mRNA levels and insulin secretion by extracellular glucose, and present evidence that islet responsiveness can be divided into two temporal phases: an early response, apparently under post-transcriptional control, and a late phase in which insulin messenger accumulates."( Regulation and specificity of glucose-stimulated insulin gene expression in human islets of Langerhans.
Ashcroft, SJ; Gray, DW; Hammonds, P; Schofield, PN; Sutton, R, 1987
)
0.27
" With lesser concentrations of glucose, the flush exhibits dose-response relationships, and with 3 mg/ml glucose, a second flush can be elicited by restoring basal conditions and stimulating anew with 3 mg/ml glucose."( Rapid transient efflux of phosphate ions from pancreatic islets as an early action of insulin secretagogues.
Bonnar, J; Dawson, RM; Freinkel, N; Younsi, CE, 1974
)
0.25
" The dose-response curve for all four effects shows peak activity at 2 microg/ml."( Inhibitory and stimulatory effects of concanavalin A on the response of mouse spleen cell suspensions to antigen. I. Characterization of the inhibitory cell activity.
Dutton, RW, 1972
)
0.25
" The trichloroacetic acid-precipitable protein of rabbit plasma incorporated virtually identical quantities of [4,5-3H]leucine in the absence or presence of TM, under the above dosage regimens, while, at the same time, a large decrease in the incorporation of [2-3H]mannose was observed in the plasma proteins of rabbits treated with TM."( Effect of tunicamycin on appearance of carbohydrate variants of plasminogen in rat and rabbit plasma.
Bretthauer, RK; Castellino, FJ; Powell, JR, 1981
)
0.44
"A detailed dose-response study relating mannose and glucose oxidation with the induction of 45Ca uptake and insulin release was performed using in vitro incubation of collagenase digested rat islets of Langerhans."( Metabolism, 45Ca uptake and insulin releasing capacities of glucose and mannose.
Ishibashi, F; Kawate, R; Onari, K; Sato, T; Tsubota, M, 1980
)
0.76
" All the effects of Con A, that is, on the peak amplitude, desensitization, dose-response relationship of ACh induced current and binding of [3H]alpha-bungarotoxin, could be recovered by D-mannose, a competitive inhibitor of Con A binding to its receptor."( Interaction of concanavalin A and wheat germ agglutinin with Helix acetylcholine receptors.
Arvanov, VL; Ayrapetian, SN; Tsai, MC; Walker, RJ, 1993
)
0.48
" Dose-response curves revealed that LcH caused 30% histamine release at 2 micrograms/ml with IgE+ sensitized cells, whereas the same release with IgE- cells required sixfold higher concentrations."( Lectins do not distinguish between heterogenous IgE molecules as defined by differential activity of an IgE-dependent histamine releasing factor.
Kagey-Sobotka, A; Kleine-Tebbe, J; Lichtenstein, LM; MacDonald, SM; MacGlashan, DW, 1996
)
0.29
" No side effects were observed for this dosage regimen."( Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I.
Alton, G; Etchison, JR; Freeze, HH; Kjaergaard, S; Skovby, F, 1997
)
0.63
" The quantitative effect of this on pharmacokinetic area under the curve was calculated and shown to be relatively minor for three of the four molecules studied, but, depending on the dosing regimen and the relative level of the high-mannose glycan, this can also have significant impact."( High-mannose glycans on the Fc region of therapeutic IgG antibodies increase serum clearance in humans.
Bondarenko, PV; Flynn, GC; Goetze, AM; Lee, E; Liu, YD; Shah, B; Zhang, Z, 2011
)
1.07
" In conclusion, this study suggested that precisely controlling the dosage and time of PA-MSHA administration can effectively increase the rat survival rate post CLP, which may be mediated through regulating inflammatory mediators and inducing endotoxin tolerance."( Effects of Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA) pretreatment on septic rats.
Cao, T; Shen, L; Wang, S; Wang, W; Zhao, F; Zhu, H, 2013
)
0.67
" A dosage of 20 mg/l BF-OU5 initiated more than 92."( Characterization and flocculability of a novel proteoglycan produced by Talaromyces trachyspermus OU5.
Fang, D; Shi, C, 2016
)
0.43
"Mannosylated polymeric nanoparticles (NPs) enable improvement of brain bioavailability and reduction of dosing due to efficient drug delivery at the target site."( Targeted delivery of mannosylated-PLGA nanoparticles of antiretroviral drug to brain.
Parikh, RH; Patel, BK; Patel, N, 2018
)
0.48
" In addition to favorable in vivo safety profiles following intratracheal administration, a single dose of the drugamers sustained ciprofloxacin dosing in lungs and AMs above the minimum inhibitory concentration (MIC) over at least a 48 h period."( Macrophage-targeted drugamers with enzyme-cleavable linkers deliver high intracellular drug dosing and sustained drug pharmacokinetics against alveolar pulmonary infections.
Chen, J; Convertine, AJ; Lee, B; Ratner, DM; Skerrett, SJ; Srinivasan, S; Stayton, PS; Su, FY; West, TE, 2018
)
0.48
" Pulmonary administration represents a promising alternative to systemic dosing for delivering antibiotics directly to the lung."( Glycan targeted polymeric antibiotic prodrugs for alveolar macrophage infections.
Chen, J; Convertine, AJ; Das, D; Lee, B; Monroe-Jones, T; Radella, F; Ratner, DM; Skerrett, SJ; Son, HN; Srinivasan, S; Stayton, PS; Su, FY; West, TE; Whittington, D, 2019
)
0.51
" AvFc showed an extended serum half-life in rats and rhesus macaques, while no discernible toxicity was observed upon repeated systemic dosing in mice."( Engineering of a Lectibody Targeting High-Mannose-Type Glycans of the HIV Envelope.
Dent, MW; Grooms, TN; Hamorsky, KT; Hanson, CV; Hume, SD; Husk, AS; Kouokam, JC; Matoba, N; Morris, MK; Rogers, KA; Villinger, F, 2019
)
0.78
" Therefore, the MTX-MAN NPs sharply reduced the drug dosage and decreased the toxicity to normal cells and tissues."( Dual-self-recognizing, stimulus-responsive and carrier-free methotrexate-mannose conjugate nanoparticles with highly synergistic chemotherapeutic effects.
Fan, Z; Hou, Z; Huang, D; Jiang, B; Sun, H; Wang, Y; Xiang, S; Xie, L; Yin, W; Zuo, W, 2020
)
0.79
" Enhanced delivery and targetability can ascertain improved bioavailability, reduced toxicity, decreased frequency of dosing and therefore better patient compliance."( 2 Receptor Specific Ligand Conjugated Nanocarriers: An Effective Strategy for Targeted Therapy of Tuberculosis.
Chaubey, P; Damani, M; Fernandes, T; Narayanan, S; Prabhu, P; Sawarkar, S, 2022
)
0.72
" More studies are required in the utility of each treatment, with some emphasis on larger sample sizes and clarifications regarding dosing and formulation."( Non-antibiotic Approaches to Preventing Pediatric UTIs: a Role for D-Mannose, Cranberry, and Probiotics?
Ching, CB, 2022
)
0.96
" However, its high polarity leads to poor absorption and consequent high dosage in humans, causing unwanted side effects."( Synthesis of 2-Acetamido-1,3,4-Tri-O-Acetyl-2-Deoxy-D-Mannopyranose -6-Phosphate Prodrugs as Potential Therapeutic Agents.
Morewood, J; Pertusati, F, 2022
)
0.72
" However, in combination, they achieved up to 100% protection when dosed 24 h post infection."( Combination treatment of mannose and GalNAc conjugated small interfering RNA protects against lethal Marburg virus infection.
Borisevich, V; Cross, RW; Geisbert, TW; Heyes, J; Holland, R; McClintock, K; Palmer, L; Pasetka, C; Samaridou, E; Wood, M; Ye, X, 2023
)
1.21
"The current work is focused on developing mannose-coated PLGA nanoparticles for delivering Donepezil and Memantine in one dosage form."( Combining donepezil and memantine via mannosylated PLGA nanoparticles for intranasal delivery: Characterization and preclinical studies.
Bhatta, RS; Ghose, S; Handa, M; Patil, GP; Sanap, SN; Shukla, R; Singh, DP, 2023
)
1.17
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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
D-aldohexoseAny D-aldose having a chain of six carbon atoms in the molecule.
D-mannoseA mannose with D-configuration.
mannopyranoseThe pyranose form of mannose.
[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 (31)

PathwayProteinsCompounds
Metabolism14961108
Carbohydrate metabolism173120
Lysosomal oligosaccharide catabolism48
Galactose Metabolism1234
Fructose and Mannose Degradation1830
Galactosemia1234
Fructosuria1830
Fructose Intolerance, Hereditary1830
Metabolism of proteins1058144
Amino Sugar and Nucleotide Sugar Metabolism2229
Post-translational protein modification666112
Asparagine N-linked glycosylation16478
N-glycan trimming in the ER and Calnexin/Calreticulin cycle186
Calnexin/calreticulin cycle86
ER Quality Control Compartment (ERQC)35
Transport to the Golgi and subsequent modification8518
N-glycan trimming and elongation in the cis-Golgi24
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc201
N-glycan antennae elongation in the medial/trans-Golgi2013
Reactions specific to the complex N-glycan synthesis pathway1010
Fructose and Mannose metabolism ( Fructose and Mannose metabolism )2527
plant arabinogalactan type II degradation04
1,5-anhydrofructose degradation111
D-galactose degradation I (Leloir pathway)1046
superpathway of CMP-sialic acids biosynthesis1460
CMP-2-keto-3-deoxy-D-glycero-D-galacto-nononate biosynthesis419
mannitol degradation II115
galactose degradation I (Leloir pathway)526
mannose degradation36
GDP-mannose metabolism19
Mannose catabolism04

Protein Targets (6)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
chromobox protein homolog 1Homo sapiens (human)Potency100.00000.006026.168889.1251AID540317
transcriptional regulator ERG isoform 3Homo sapiens (human)Potency50.11870.794321.275750.1187AID624246
DNA polymerase kappa isoform 1Homo sapiens (human)Potency13.37140.031622.3146100.0000AID588579
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Alpha-mannosidase 2C1Rattus norvegicus (Norway rat)IC50 (µMol)20,000.00001.75001.75001.7500AID108106
Fucose-binding lectin PA-IILPseudomonas aeruginosa PAO1IC50 (µMol)100.50000.91002.13002.7400AID1526585; AID1526586
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (19)

Processvia Protein(s)Taxonomy
regulation of T cell proliferationCD209 antigenHomo sapiens (human)
adaptive immune responseCD209 antigenHomo sapiens (human)
endocytosisCD209 antigenHomo sapiens (human)
heterophilic cell-cell adhesion via plasma membrane cell adhesion moleculesCD209 antigenHomo sapiens (human)
leukocyte cell-cell adhesionCD209 antigenHomo sapiens (human)
cell-cell recognitionCD209 antigenHomo sapiens (human)
virion attachment to host cellCD209 antigenHomo sapiens (human)
viral genome replicationCD209 antigenHomo sapiens (human)
antigen processing and presentationCD209 antigenHomo sapiens (human)
intracellular signal transductionCD209 antigenHomo sapiens (human)
positive regulation of T cell proliferationCD209 antigenHomo sapiens (human)
innate immune responseCD209 antigenHomo sapiens (human)
symbiont entry into host cellCD209 antigenHomo sapiens (human)
peptide antigen transportCD209 antigenHomo sapiens (human)
intracellular transport of virusCD209 antigenHomo sapiens (human)
B cell adhesionCD209 antigenHomo sapiens (human)
positive regulation of viral life cycleCD209 antigenHomo sapiens (human)
immune responseCD209 antigenHomo sapiens (human)
biological process involved in interspecies interaction between organismsCD209 antigenHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (7)

Processvia Protein(s)Taxonomy
virus receptor activityCD209 antigenHomo sapiens (human)
protein bindingCD209 antigenHomo sapiens (human)
mannose bindingCD209 antigenHomo sapiens (human)
carbohydrate bindingCD209 antigenHomo sapiens (human)
peptide antigen bindingCD209 antigenHomo sapiens (human)
virion bindingCD209 antigenHomo sapiens (human)
metal ion bindingCD209 antigenHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (7)

Processvia Protein(s)Taxonomy
extracellular regionCD209 antigenHomo sapiens (human)
cytoplasmCD209 antigenHomo sapiens (human)
plasma membraneCD209 antigenHomo sapiens (human)
external side of plasma membraneCD209 antigenHomo sapiens (human)
cell surfaceCD209 antigenHomo sapiens (human)
membraneCD209 antigenHomo sapiens (human)
host cellCD209 antigenHomo sapiens (human)
external side of plasma membraneCD209 antigenHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (43)

Assay IDTitleYearJournalArticle
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.
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.
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.
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.
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.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID709912Displacement of biotinylated-TM PAA from human MMR at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID1072562Displacement of [125I]-Man30-BSA from DC-SIGN receptor carbohydrate recognition domain (unknown origin) after 2 hrs by gamma-counting analysis2014European journal of medicinal chemistry, Mar-21, Volume: 75Monovalent mannose-based DC-SIGN antagonists: targeting the hydrophobic groove of the receptor.
AID30427Compound was tested for inhibition of Human acrosin by aldohexoses1981Journal of medicinal chemistry, Nov, Volume: 24, Issue:11
Inhibition of human acrosin by monosaccharides and related compounds: structure-activity relationships.
AID596531Displacement of yeast mannan from Concanavalin A by Enzyme-linked lectin assay2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
Synthesis of glycopeptide dendrimers, dimerization and affinity for Concanavalin A.
AID709915Displacement of biotinylated-TM PAA from human MBP at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID1526586Competitive inhibition of N-(fluorescein-5-yl)-N'-(alpha-L-fucopyranosyl ethylen)-thiocarbamide binding to Pseudomonas aeruginosa PA14 LecB after 8 to 22 hrs by fluorescence polarization assay2019Journal of medicinal chemistry, 10-24, Volume: 62, Issue:20
Anti-biofilm Agents against
AID1526585Inhibition of Pseudomonas aeruginosa PAO1 LecB after 6 hrs by fluorescence polarization assay2019Journal of medicinal chemistry, 10-24, Volume: 62, Issue:20
Anti-biofilm Agents against
AID709914Displacement of biotinylated-TM PAA from human DC-SIGN at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID709926Displacement of biotinylated-TM PAA from Escherichia coli FimH expressed in Escherichia coli HM125 at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID241553Inhibitory concentration against mannan binding relative to concanavalin A; Using QCM(quartz crystal microbalance) assay2005Bioorganic & medicinal chemistry letters, Jun-02, Volume: 15, Issue:11
Redox-responsive and calcium-dependent switching of glycosyldisulfide interactions with Concanavalin A.
AID381596Inhibition of Cryptosporidium parvum recombinant Galactose/N-acetylgalactosamine-specific lectin binding to Caco2A cells2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID381597Inhibition of Cryptosporidium parvum recombinant Galactose/N-acetylgalactosamine-specific lectin binding to Caco2A cells relative to galactose2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID709911Displacement of biotinylated-TM PAA from human SP-D at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID709910Displacement of biotinylated-TM PAA from human langerin at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID587707Inhibition of Drosophila melanogaster GM2b at 5 mM by spectrophotometry2011European journal of medicinal chemistry, Mar, Volume: 46, Issue:3
α-D-mannose derivatives as models designed for selective inhibition of Golgi α-mannosidase II.
AID30429Compound was tested for inhibition of Human acrosin by aldoses1981Journal of medicinal chemistry, Nov, Volume: 24, Issue:11
Inhibition of human acrosin by monosaccharides and related compounds: structure-activity relationships.
AID1459743Inhibition of DLODP in human HepG2 microsomal membrane assessed as reduction in [3H]OSP production at 50 mM using Glc3-0[3H]Man9-5GlcNAc2-PP-dolichol as substrate at pH 5.5 measured after 20 to 60 mins by scintillation counting2017European journal of medicinal chemistry, Jan-05, Volume: 125Synthesis and biological evaluation of chemical tools for the study of Dolichol Linked Oligosaccharide Diphosphatase (DLODP).
AID709908Displacement of biotinylated-TM PAA from human DLEC at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID381592Anticryptosporidial activity against Cryptosporidium parvum GCH1 assessed as inhibition of rabbit erythrocytes hemagglutinination2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID381594Anticryptosporidial activity against Cryptosporidium hominis TU502 assessed as inhibition of rabbit erythrocytes hemagglutinination2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID587709Inhibition of Drosophila melanogaster LM408 at 5 mM by spectrophotometry2011European journal of medicinal chemistry, Mar, Volume: 46, Issue:3
α-D-mannose derivatives as models designed for selective inhibition of Golgi α-mannosidase II.
AID1524940Binding affinity to Jack bean Concanavalin A by SPR assay2019Bioorganic & medicinal chemistry letters, 05-15, Volume: 29, Issue:10
Modulation of the NOD-like receptors NOD1 and NOD2: A chemist's perspective.
AID381595Anticryptosporidial activity against Cryptosporidium hominis TU502 assessed as inhibition of rabbit erythrocytes hemagglutinination relative to galactose2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID500279Ratio of Kcat to Km for Neisseria meningitidis lgtC2006Nature chemical biology, Dec, Volume: 2, Issue:12
Using substrate engineering to harness enzymatic promiscuity and expand biological catalysis.
AID596532Ratio of methyl alpha-D-mannoside IC50 to compound IC50 for binding affinity to Concanavalin A per carbohydrate moiety2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
Synthesis of glycopeptide dendrimers, dimerization and affinity for Concanavalin A.
AID381593Anticryptosporidial activity against Cryptosporidium parvum GCH1 assessed as inhibition of rabbit erythrocytes hemagglutinination relative to galactose2007The Journal of biological chemistry, Nov-30, Volume: 282, Issue:48
Cryptosporidium p30, a galactose/N-acetylgalactosamine-specific lectin, mediates infection in vitro.
AID709909Displacement of biotinylated-TM PAA from human Dectin-2 at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
AID596530Ratio of methyl alpha-D-mannoside IC50 to compound IC50 for binding affinity to Concanavalin A2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
Synthesis of glycopeptide dendrimers, dimerization and affinity for Concanavalin A.
AID108106Inhibitory activity against Mannosidase in jack bean (Canavalia ensiformis)1989Journal of medicinal chemistry, Sep, Volume: 32, Issue:9
Design of potential anti-HIV agents. 1. Mannosidase inhibitors.
AID709913Displacement of biotinylated-TM PAA from human DC-SIGNR at 50 mM after 3 hrs by colorimetry2012Journal of medicinal chemistry, Nov-26, Volume: 55, Issue:22
Target Selectivity of FimH Antagonists.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9,480)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904096 (43.21)18.7374
1990's1404 (14.81)18.2507
2000's1547 (16.32)29.6817
2010's1717 (18.11)24.3611
2020's716 (7.55)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 59.86

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 Index59.86 (24.57)
Research Supply Index9.18 (2.92)
Research Growth Index4.53 (4.65)
Search Engine Demand Index215.11 (26.88)
Search Engine Supply Index3.97 (0.95)

This Compound (59.86)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials41 (0.42%)5.53%
Reviews296 (3.05%)6.00%
Case Studies58 (0.60%)4.05%
Observational0 (0.00%)0.25%
Other9,303 (95.93%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]