Page last updated: 2024-09-27

allose

Cross-References

ID SourceID
PubMed CID439507
CHEMBL ID1222152
CHEBI ID4093
CHEBI ID37690
CHEBI ID17393
CHEBI ID37742
SCHEMBL ID60362
MeSH IDM0042519

Synonyms (28)

Synonym
CHEMBL1222152
ALL ,
CHEBI:4093 ,
ALLOSE ,
C01487
d-allose ,
allose, d-
579-36-2
nsc-144657
d-allopyranose ,
DB03989
BMSE000008
AKOS006272674
BMSE000808
BMSE001008
SCHEMBL60362
d-all
allopyranose
d-allopyranoside
allopyranoside
Q27106301
DTXSID201015878
d-allo-hexose
dtxcid501474033
chebi:37690
allo-hexose
chebi:17393
chebi:37742

Research Excerpts

Overview

ExcerptReference
"D-allose is a rare sugar that has been reported to up-regulate thioredoxin-interacting protein (TXNIP) expression and affect the production of intracellular reactive oxygen species (ROS). "( Akimitsu, K; Haba, R; Ibuki, E; Izumori, K; Kakehi, Y; Matsuoka, Y; Sugimoto, M; Taoka, R; Tohi, Y; Yoshihara, A; Zhang, X, 2022)
"D-Allose is a rare cis-caprose with a wide range of physiological functions, which has a wide range of applications in medicine, food, and other industries. "( Chen, Y; Dong, S; Duan, S; Li, Z; Ma, C; Wang, G; Wang, R; Wang, Y; Wu, Y, 2023)
"d-Allose is an aldohexose of the C3-epimer of d-glucose, existing in very small amounts in nature, called a rare sugar. "( Kamitori, S, 2023)
"d-Allose is a low-calorie rare sugar with great application potential in the food and pharmaceutical industries. "( Gao, X; Guan, L; Li, C; Liu, W; Lu, F; Qin, HM; Wang, F; Wang, J; Wei, M; Zhang, W, 2023)
"d-Allose is a rare sugar that has been reported to have some unique physiological effects."( Ibaraki, M; Kinoshita, T; Kudomi, N; Nishiyama, Y; Tago, T; Toyohara, J; Wada, K; Yamamoto, H; Yamamoto, Y, 2019)
"D-Allose is a rare sugar, can be used as an ingredient in a range of foods and dietary supplements, has alimentary activities, especially excellent anti-cancer effects and used in assisting cancer chemotherapy and radiotherapy, etc. "( Du, K; Gao, L; Li, C; Lin, H; Lin, J; Ren, Y, 2020)
"D‑allose is a rare sugar which has been shown to have growth inhibitory effects in several kinds of malignancies. "( Hossain, A; Kadowaki, N; Kamitori, K; Kanaji, N; Katagi, A; Noguchi, C; Tokuda, M, 2018)
"D-Allose is a rare monosaccharide, which rarely appears in the natural environment. "( Chen, J; Chen, Z; Guang, C; Mu, W; Zhang, T; Zhang, W, 2018)
"D-allose is a monosaccharide. "( Asaga, T; Chujo, K; Iwanaga, Y; Ono, J; Taie, S; Ueki, M, 2008)
"D-Allose is a monosaccharide (C-3 epimer of glucose) distributed rarely in nature; because of its scarcity and cost, the biological effect has hardly been studied."( Chung, BC; Jo, MJ; Kim, MO; Kim, SH; Lee, HY; Naha, N, 2008)
"d-Allose is a novel anti-tumor monosaccharide that causes cell growth inhibition, specifically of the cancer cells, by inducing the tumor suppressor gene thioredoxin interacting protein (TXNIP). "( Dong, Y; Horii, M; Kamitori, K; Sanada, K; Sui, L; Tokuda, M; Yamaguchi, F, 2008)
"D-allose is an aldo-hexose present in nature that recently has been demonstrated to inhibit production of inflammatory mediators in septic kidneys."( Asaga, T; Miyawaki, Y; Shirakami, G; Tokuda, M; Ueki, M; Ueno, M, 2012)

Effects

ExcerptReference
"D-Allose has an 80% sweetness relative to table sugar but is ultra-low calorie and non-toxic and is thus an ideal candidate to take the place of table sugar in food products."( Chen, J; Chen, Z; Guang, C; Mu, W; Zhang, T; Zhang, W, 2018)
"D-allose has a considerable potential as a new anticancer agent in those patients."( Hoshikawa, H; Hosokawa, T; Kamitori, K; Mitani, T; Mori, N; Mori, T; Tokuda, M; Tsukamoto, I; Yamaguchi, F, 2009)
"D-Allose has been demonstrated to exert many physiological functions."( Akimitsu, K; Hoshino, K; Miyake, M; Miyazaki, R; Suzuki, M; Takao, K, 2022)
"d-allose has the biological activity to protect against ischemia-reperfusion injury, however, the underlying mechanism remains unclear."( Fei, Z; Fu, YH; Gao, DK; Gou, MR; Luo, YW; Zhang, L; Zhang, M, 2023)
"D-allose has shown great promise for combating tumor cells with no side effects, especially in combination with first-line drugs; however, its potential for cancer therapy has not been comprehensively investigated in vitro or in vivo."( Ganjavi, M; Khajeh, S; Panahi, G; Razban, V; Tahami, SM; Zare, M, 2023)
"D-Allose has an 80% sweetness relative to table sugar but is ultra-low calorie and non-toxic and is thus an ideal candidate to take the place of table sugar in food products."( Chen, J; Chen, Z; Guang, C; Mu, W; Zhang, T; Zhang, W, 2018)
"As d-allose has no known side effects on normal cells, the combination of d-allose and 5-FU might be a potent candidate for cancer therapy."( Dong, Y; Horii, M; Kamitori, K; Sanada, K; Sui, L; Tokuda, M; Yamaguchi, F, 2008)
"D-allose has a considerable potential as a new anticancer agent in those patients."( Hoshikawa, H; Hosokawa, T; Kamitori, K; Mitani, T; Mori, N; Mori, T; Tokuda, M; Tsukamoto, I; Yamaguchi, F, 2009)
"D-allose has attracted a great deal of attention in recent years due to its many pharmaceutical activities, which include anti-cancer, anti-tumor, anti-inflammatory, anti-oxidative, anti-hypertensive, cryoprotective, and immunosuppressant activities. "( Lim, YR; Oh, DK, 2011)

Treatment

ExcerptReference
"D-allose treatment inhibited the proliferation of U251MG and U87MG cells in a dose-dependent manner (3-50 mM)."( Akimitsu, K; Fujimori, T; Izumori, K; Kanda, T; Miyake, K; Nishiyama, A; Ogawa, D; Ohsaki, H; Rahman, A; Shibayama, Y; Suzuki, K; Tamiya, T; Ye, J, 2023)
"D-allose treatment significantly suppressed the MPO activity and the number of MPO-positive cells compared with those in the vehicle group, suggesting that treatment with D-allose can reduce the infiltration of leukocytes into the ischemic tissue."( Fei, Z; Gao, D; Kawai, N; Lu, F; Nakamura, T; Tamiya, T, 2013)
"D-allose treatment of isolated islet culture prior to transplantation restored islet function and increased successful transplant rate. "( Akamoto, S; Asano, E; Hossain, A; Kashiwagi, H; Noguchi, C; Okano, K; Sui, L; Suzuki, Y; Tokuda, M, 2016)
"D-allose-treated cells."( Colby-Germinario, S; Germinario, RJ; Manuel, S; Pratt, SE, 1994)
"Co-treatment of D-allose and the antioxidant L-glutathione canceled the D-allose-induced reduction in cell viability and intracellular ROS elevation."( Akimitsu, K; Haba, R; Ibuki, E; Izumori, K; Kakehi, Y; Matsuoka, Y; Sugimoto, M; Taoka, R; Tohi, Y; Yoshihara, A; Zhang, X, 2022)
"Treatment of D-allose also significantly decreased the number of COX-2-positive cells and microglial activation in the ischemic tissue."( Fei, Z; Gao, D; Kawai, N; Lu, F; Nakamura, T; Tamiya, T, 2013)

Roles (1)

RoleDescription
antioxidantA substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
[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 (2)

ClassDescription
D-allose
allopyranose
[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)

allose is involved in 2 pathway(s), involving a total of 9 unique proteins and 17 unique compounds

PathwayProteinsCompounds
D-Allulose Degradation69
D-allose degradation38

Bioassays (1)

Assay IDTitleYearJournalArticle
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (151)

TimeframeStudies, This Drug (%)All Drugs %
pre-199015 (9.93)18.7374
1990's10 (6.62)18.2507
2000's42 (27.81)29.6817
2010's59 (39.07)24.3611
2020's25 (16.56)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews5 (3.27%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other148 (96.73%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Safety/Toxicity (3)

ArticleYear
Thermal degradation of agar: Mechanism and toxicity of products.
Food chemistry, Oct-30, Volume: 264
2018
D-allose ameliorates cisplatin-induced nephrotoxicity in mice.
The Tohoku journal of experimental medicine, Volume: 228, Issue: 3
2012
Acute and sub-chronic toxicity of D-allose in rats.
Bioscience, biotechnology, and biochemistry, Volume: 74, Issue: 7
2010
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Dosage (1)

ArticleYear
D-allose and D-psicose reinforce the action of metronidazole on trichomonad.
Parasitology research, Volume: 110, Issue: 4
2012
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Interactions (1)

ArticleYear
Additive antitumour effect of D‑allose in combination with cisplatin in non-small cell lung cancer cells.
Oncology reports, Volume: 39, Issue: 3
2018
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]