Maltose (BioDeep_00000014323)
Secondary id: BioDeep_00000014974
natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019
代谢物信息卡片
化学式: C12H22O11 (342.1162062)
中文名称: D-(+)-麦芽糖, D-(+)-麦芽糖一水合物, 麦芽糖浆, D-麦芽糖
谱图信息:
最多检出来源 Homo sapiens(plant) 41.14%
Last reviewed on 2024-09-14.
Cite this Page
Maltose. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/maltose (retrieved
2024-12-04) (BioDeep RN: BioDeep_00000014323). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O
InChI: InChI=1/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5-,6+,7-,8-,9-,10-,11?,12-/m1/s1
描述信息
D-Maltose, also known as maltose, maltobiose or malt sugar, is a disaccharide formed from two units of glucose joined with an alpha (1→4) bond. Its name comes from malt, combined with the suffix -ose which is used in names of sugars. Maltose is a key structural motif of starch. When alpha-amylase breaks down starch, it removes two glucose units at a time, producing maltose. Maltose can be further broken down to glucose by the maltase enzyme, which catalyses the hydrolysis of the glycosidic bond. D-maltose exists in all living species, ranging from bacteria to plants to humans. Within humans, D-maltose participates in a number of enzymatic reactions. In particular, maltose can be converted into glucose; which is mediated by the enzyme maltase-glucoamylase. In addition, maltose can be converted into glucose through its interaction with the enzyme glycogen debranching enzyme. Maltose is found in high concentrations in oriental wheats and in a lower concentrations in sweet potato, grape wines, yellow pond-lilies, sunflowers, and spinach. Maltose is a component of malt, a substance which is obtained in the process of allowing grain to soften in water and germinate. It is also present in highly variable quantities in partially hydrolysed starch products like maltodextrin, corn syrup and acid-thinned starch. Maltose has a sweet taste but is only about 30–60\\\\% as sweet as sucrose, depending on the concentration.
Sweetening agent, dietary supplement. Occurs in some plants as hydrolytic dec. production of starch. Production in high yield (80\\\\%) by the action of diastase (a- and b-amylase) on starch, a process used in brewing
D000074385 - Food Ingredients > D005503 - Food Additives
D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents
Maltose is a disaccharide formed from two units of glucose joined with an α(1→4) bond, a reducing sugar. Maltose monohydrate can be used as a energy source for bacteria.
Maltose is a disaccharide formed from two units of glucose joined with an α(1→4) bond, a reducing sugar. Maltose monohydrate can be used as a energy source for bacteria.
同义名列表
46 个代谢物同义名
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(2R,3S,4R,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxane-3,4,5-triol; 1-alpha-delta-Glucopyranosyl-4-alpha-delta-glucopyranose; alpha-delta-Glucopyranosyl-(1->4)-delta-glucopyranose; 4-(alpha-delta-Glucopyranosido)-alpha-glucopyranose; 4-O-alpha-delta-Glucopyranosyl-delta-glucopyranose; 4-O-alpha-D-Glucopyranosyl-alpha-D-mannopyranose; 1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose; alpha-delta-Glucopyranosyl-(1->4)-delta-glucose; 4-(alpha-D-Glucopyranosido)-alpha-glucopyranose; alpha-D-Glucopyranosyl-(1->4)-D-glucopyranose; 4-O-alpha-delta-Glucopyranosyl-delta-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucopyranose; 4-O-a-D-Glucopyranosyl-a-D-mannopyranose; 4-O-Α-D-glucopyranosyl-α-D-mannopyranose; 4-(alpha-delta-Glucosido)-delta-glucose; alpha-D-Glucopyranosyl-(1->4)-D-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucose; alpha-delta-GLCP-(1->4)-delta-GLCP; 4-O-a-D-Glucopyranosyl-D-glucose; 4-(alpha-D-Glucosido)-D-glucose; alpha-D-GLCP-(1->4)-D-GLCP; delta-(+)-Maltose; alpha-Malt sugar; Maltose solution; D-(+)-Maltose; Cextromaltose; delta-Maltose; Advantose 100; Maltose HHH; Maltose HH; Finetose F; Maltodiose; Malt sugar; Malzzucker; Maltobiose; D-Maltose; Martos-10; Sunmalt S; Finetose; Sunmalt; Madoros; Maltose; Maltos; D-Maltose; L-Glc(a1-4)a-L-Glc; Maltose
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:140774
- ChEBI: CHEBI:17306
- ChEBI: CHEBI:47937
- KEGG: C00208
- KEGGdrug: D00044
- PubChem: 10991489
- PubChem: 439186
- HMDB: HMDB0000163
- Metlin: METLIN413
- DrugBank: DB03323
- Wikipedia: Maltose
- MeSH: Maltose
- KNApSAcK: C00001140
- foodb: FDB001193
- chemspider: 9166684
- CAS: 69-79-4
- MoNA: PS005706
- PubChem: 3508
- PDB-CCD: MAL
- PDB-CCD: N9S
- 3DMET: B04649
- NIKKAJI: J4.871B
- medchemexpress: HY-N2024
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-549
- KNApSAcK: 17306
- LOTUS: LTS0038046
分类词条
相关代谢途径
Reactome(9)
BioCyc(8)
代谢反应
26 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
COVID-19 Disease Map(0)
PathBank(25)
- Starch and Sucrose Metabolism:
D-Glucose + [PTS enzyme I]-N -phospho-L-histidine ⟶ -D-glucose 1-phosphate + [PTS enzyme I]-L-histidine
- Starch and Sucrose Metabolism:
-D-Glucose + Unknown ⟶ -D-Glucose 6-phosphate + Unknown
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Adenosine triphosphate + D-Glucose ⟶ Adenosine diphosphate + Glucose 6-phosphate
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
PharmGKB(0)
72 个相关的物种来源信息
- 3701 - Arabidopsis: LTS0038046
- 3702 - Arabidopsis thaliana:
- 3702 - Arabidopsis thaliana: 10.1104/PP.114.240986
- 3702 - Arabidopsis thaliana: 10.1111/TPJ.14311
- 3702 - Arabidopsis thaliana: 10.3390/IJMS17091565
- 3702 - Arabidopsis thaliana: LTS0038046
- 4454 - Araceae: LTS0038046
- 13345 - Ardisia crenata: 10.3389/FMOLB.2021.683671
- 6656 - Arthropoda: LTS0038046
- 4890 - Ascomycota: LTS0038046
- 91061 - Bacilli: LTS0038046
- 2 - Bacteria: LTS0038046
- 6658 - Branchiopoda: LTS0038046
- 3700 - Brassicaceae: LTS0038046
- 5475 - Candida: LTS0038046
- 5476 - Candida albicans: 10.1007/S11306-016-1134-2
- 5476 - Candida albicans: LTS0038046
- 3051 - Chlamydomonadaceae: LTS0038046
- 3052 - Chlamydomonas: LTS0038046
- 3055 - Chlamydomonas reinhardtii: 10.1111/TPJ.12747
- 3055 - Chlamydomonas reinhardtii: LTS0038046
- 3166 - Chlorophyceae: LTS0038046
- 3041 - Chlorophyta: LTS0038046
- 6668 - Daphnia: LTS0038046
- 6669 - Daphnia pulex: 10.1038/SREP25125
- 6669 - Daphnia pulex: LTS0038046
- 77658 - Daphniidae: LTS0038046
- 766764 - Debaryomycetaceae: LTS0038046
- 7227 - Drosophila melanogaster: 10.1038/S41467-019-11933-Z
- 543 - Enterobacteriaceae: LTS0038046
- 33682 - Euglenozoa: LTS0038046
- 2759 - Eukaryota: LTS0038046
- 3803 - Fabaceae: LTS0038046
- 4751 - Fungi: LTS0038046
- 1236 - Gammaproteobacteria: LTS0038046
- 9606 - Homo sapiens: -
- 5653 - Kinetoplastea: LTS0038046
- 4469 - Lemna: LTS0038046
- 89585 - Lemna aequinoctialis: 10.1371/JOURNAL.PONE.0187622
- 89585 - Lemna aequinoctialis: LTS0038046
- 161103 - Lemna perpusilla: 10.1371/JOURNAL.PONE.0187622
- 4447 - Liliopsida: LTS0038046
- 3398 - Magnoliopsida: LTS0038046
- 3877 - Medicago: LTS0038046
- 3879 - Medicago sativa: 10.3389/FPLS.2017.01208
- 3879 - Medicago sativa: LTS0038046
- 50362 - Melanthiaceae: LTS0038046
- 33208 - Metazoa: LTS0038046
- 2511164 - Microchloropsis: 10.3389/FPLS.2020.00981
- 3498 - Morus alba L.: -
- 49669 - Paris: LTS0038046
- 83858 - Paris fargesii: 10.1016/J.JPROT.2019.02.003
- 83858 - Paris fargesii: LTS0038046
- 49666 - Paris polyphylla: 10.1016/J.JPROT.2019.02.003
- 49666 - Paris polyphylla: LTS0038046
- 33090 - Plants: -
- 180039 - Psychotria punctata: 10.3389/FMOLB.2021.683671
- 4891 - Saccharomycetes: LTS0038046
- 590 - Salmonella: LTS0038046
- 28901 - Salmonella enterica: 10.1021/ACS.JPROTEOME.0C00281
- 28901 - Salmonella enterica: LTS0038046
- 90964 - Staphylococcaceae: LTS0038046
- 1279 - Staphylococcus: LTS0038046
- 1280 - Staphylococcus aureus: LTS0038046
- 35493 - Streptophyta: LTS0038046
- 58023 - Tracheophyta: LTS0038046
- 5690 - Trypanosoma: LTS0038046
- 5691 - Trypanosoma brucei: 10.1371/JOURNAL.PNTD.0001618
- 5691 - Trypanosoma brucei: LTS0038046
- 5654 - Trypanosomatidae: LTS0038046
- 33090 - Viridiplantae: LTS0038046
- 29760 - Vitis vinifera: 10.1016/J.DIB.2020.106469
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Xinyue Zhai, Xinwei Tao, Yuqian Wu, Kesun Jin, Huaping Tan, Tianle Zhou, Yong Chen. Injectable and Self-Adaptive Gel Scaffold Based on Heparin Microspheres for Adipogenesis of Human Adipose-Derived Stem Cells.
Biomacromolecules.
2023 Sep; ?(?):. doi:
10.1021/acs.biomac.3c00348
. [PMID: 37722066] - Yuang Wu, Yue Sun, Evelyne Richet, Zhifu Han, Jijie Chai. Structural basis for negative regulation of the Escherichia coli maltose system.
Nature communications.
2023 08; 14(1):4925. doi:
10.1038/s41467-023-40447-y
. [PMID: 37582800] - Patricia Benito, Javier Bellón, Rosa Porcel, Lynne Yenush, José M Mulet. The Biostimulant, Potassium Humate Ameliorates Abiotic Stress in Arabidopsis thaliana by Increasing Starch Availability.
International journal of molecular sciences.
2023 Jul; 24(15):. doi:
10.3390/ijms241512140
. [PMID: 37569516] - Ayako Wada-Katsumata, Eduardo Hatano, Coby Schal. Gustatory polymorphism mediates a new adaptive courtship strategy.
Proceedings. Biological sciences.
2023 03; 290(1995):20222337. doi:
10.1098/rspb.2022.2337
. [PMID: 36987637] - Samantha McPherson, Ayako Wada-Katsumata, Jules Silverman, Coby Schal. Glucose- and disaccharide-containing baits impede secondary mortality in glucose-averse German cockroaches.
Journal of economic entomology.
2023 Mar; ?(?):. doi:
10.1093/jee/toad030
. [PMID: 36888567] - Liangke Chen, Xiangbai Dong, Huifang Yang, Yaru Chai, Yan Xia, Lihong Tian, Le Qing Qu. Cytosolic disproportionating enzyme2 is essential for pollen germination and pollen tube elongation in rice.
Plant physiology.
2023 01; 191(1):96-109. doi:
10.1093/plphys/kiac496
. [PMID: 36282529] - Tengfei Liu, Md Abu Kawochar, Shengxuan Liu, Yunxia Cheng, Shahnewaz Begum, Enshuang Wang, Tingting Zhou, Tiantian Liu, Xingkui Cai, Botao Song. Suppression of the tonoplast sugar transporter, StTST3.1, affects transitory starch turnover and plant growth in potato.
The Plant journal : for cell and molecular biology.
2023 01; 113(2):342-356. doi:
10.1111/tpj.16050
. [PMID: 36444716] - Mikel Redin Hurtado, Ida Fischer, Matthias Laska. Is sugar as sweet to the palate as seeds are appetizing to the belly? Taste responsiveness to five food-associated carbohydrates in zoo-housed white-faced sakis, Pithecia pithecia.
PloS one.
2023; 18(10):e0292175. doi:
10.1371/journal.pone.0292175
. [PMID: 37906563] - A Ruiz-Gayosso, I Rodríguez-Cruz, E Martínez-Barajas, P Coello. Phosphorylation of DPE2 at S786 partially regulates starch degradation.
Plant physiology and biochemistry : PPB.
2022 Dec; 193(?):70-77. doi:
10.1016/j.plaphy.2022.10.024
. [PMID: 36335878] - Avinash Kumar, Vinay Kumar Singh, Arvind M Kayastha. Molecular modeling, docking and dynamics studies of fenugreek (Trigonella foenum-graecum) α-amylase.
Journal of biomolecular structure & dynamics.
2022 Nov; ?(?):1-16. doi:
10.1080/07391102.2022.2144458
. [PMID: 36369783] - Lianyu Zhou, Lu Jiao, Jiasheng Ju, Xuelan Ma. Effect of Sodium Selenite on the Metabolite Profile of Epichloë sp. Mycelia from Festuca sinensis in Solid Culture.
Biological trace element research.
2022 Nov; 200(11):4865-4879. doi:
10.1007/s12011-021-03054-w
. [PMID: 34973128] - Michail Michailidis, Vaia Styliani Titeli, Evangelos Karagiannis, Kyriaki Feidaki, Ioannis Ganopoulos, Georgia Tanou, Anagnostis Argiriou, Athanassios Molassiotis. Tissue-specific transcriptional analysis outlines calcium-induced core metabolic changes in sweet cherry fruit.
Plant physiology and biochemistry : PPB.
2022 Oct; 189(?):139-152. doi:
10.1016/j.plaphy.2022.08.022
. [PMID: 36087439] - Yijun Liu, Yuhan Zeng, Yixin Liu, Xiaoya Wang, Yuhuan Chen, Dion Lepp, Rong Tsao, Tsuyoshi Sadakiyo, Hua Zhang, Yoshinori Mine. Regulatory Effect of Isomaltodextrin on a High-Fat Diet Mouse Model with LPS-Induced Low-Grade Chronic Inflammation.
Journal of agricultural and food chemistry.
2022 Sep; 70(36):11258-11273. doi:
10.1021/acs.jafc.2c03391
. [PMID: 36041062] - Yangyang Geng, Shixin Zhang, Ningxian Yang, Likang Qin. Whole-Genome Sequencing and Comparative Genomics Analysis of the Wild Edible Mushroom (Gomphus purpuraceus) Provide Insights into Its Potential Food Application and Artificial Domestication.
Genes.
2022 09; 13(9):. doi:
10.3390/genes13091628
. [PMID: 36140797] - Andrea Hoehnel, Jairo Salas García, Christine Coffey, Emanuele Zannini, Elke K Arendt. Comparative study of sugar extraction procedures for HPLC analysis and proposal of an ethanolic extraction method for plant-based high-protein ingredients.
Journal of the science of food and agriculture.
2022 Sep; 102(12):5055-5064. doi:
10.1002/jsfa.11204
. [PMID: 33709392] - Qiubin Huang, Huiping Liu, Juanmei Zhang, Shaowei Wang, Fengying Liu, Chengdie Li, Gang Wang. Production of extracellular amylase contributes to the colonization of Bacillus cereus 0-9 in wheat roots.
BMC microbiology.
2022 08; 22(1):205. doi:
10.1186/s12866-022-02618-7
. [PMID: 35996113] - Javad Hassanzadeh, Haider A J Al Lawati, Nafiseh Bagheri. On paper synthesis of multifunctional CeO2 nanoparticles@Fe-MOF composite as a multi-enzyme cascade platform for multiplex colorimetric detection of glucose, fructose, sucrose, and maltose.
Biosensors & bioelectronics.
2022 Jul; 207(?):114184. doi:
10.1016/j.bios.2022.114184
. [PMID: 35339073] - Yaping Ma, Yaru Han, Xuerui Feng, Handong Gao, Bing Cao, Lihua Song. Genome-wide identification of BAM (β-amylase) gene family in jujube (Ziziphus jujuba Mill.) and expression in response to abiotic stress.
BMC genomics.
2022 Jun; 23(1):438. doi:
10.1186/s12864-022-08630-5
. [PMID: 35698031] - Xiangxiang Kong, Chunxia Li, Xiaodong Sun, Bing Niu, Dehua Guo, Yuan Jiang, Jielin Yang, Qin Chen. The maltose transporter subunit IICB of the phosphotransferase system: An important factor for biofilm formation of Cronobacter.
International journal of food microbiology.
2022 Jun; 370(?):109517. doi:
10.1016/j.ijfoodmicro.2021.109517
. [PMID: 35216827] - Felix Funk, Klaus Weber, Naja Nyffenegger, Jens-Alexander Fuchs, Amy Barton. Tissue biodistribution of intravenous iron-carbohydrate nanomedicines differs between preparations with varying physicochemical characteristics in an anemic rat model.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
2022 May; 174(?):56-76. doi:
10.1016/j.ejpb.2022.03.006
. [PMID: 35337966] - Sarah Tassinari, Silvia Moreno, Hartmut Komber, Riccardo Carloni, Michela Cangiotti, Maria Francesca Ottaviani, Dietmar Appelhans. Synthesis and biological and physico-chemical characterization of glycodendrimers and oligopeptides for the treatment of systemic lupus erythematosus.
Nanoscale.
2022 Mar; 14(12):4654-4670. doi:
10.1039/d1nr06583a
. [PMID: 35262128] - Beibei Wei, Wei Xia, Lei Wang, Xuewei Jin, Weikang Yang, Deming Rao, Sheng Chen, Jing Wu. Diverse prebiotic effects of isomaltodextrins with different glycosidic linkages and molecular weights on human gut bacteria in vitro.
Carbohydrate polymers.
2022 Mar; 279(?):118986. doi:
10.1016/j.carbpol.2021.118986
. [PMID: 34980347] - Raquel López-Vilella, Silvia Lozano-Edo, Patricia Arenas Martín, Pablo Jover-Pastor, Meryem Ezzitouny, José Sorolla Romero, María Calvo Asensio, Julia Martínez-Solé, Borja Guerrero Cervera, José Carlos Sánchez Martínez, Víctor Donoso Trenado, Ignacio Sánchez-Lázaro, Luis Martinez Dolz, Luis Almenar Bonet. Impact of intravenous ferric carboxymaltose on heart failure with preserved and reduced ejection fraction.
ESC heart failure.
2022 02; 9(1):133-145. doi:
10.1002/ehf2.13753
. [PMID: 34964300] - Tomoya Goto, Tomoki Umeda, Shingo Hino, Tatsuya Morita, Naomichi Nishimura. Oral Intake of Slowly Digestible α-Glucan Such as Resistant Maltodextrin Leads to Increased Secretion of Glucagon-Like Peptide-2 in Rats and Helps Thicken Their Ileal Mucosae.
Journal of nutritional science and vitaminology.
2022; 68(2):104-111. doi:
10.3177/jnsv.68.104
. [PMID: 35491199] - Lourdes M DelRosso, Raffaele Ferri, Maida L Chen, Vidhi Kapoor, Richard P Allen, Maria Paola Mogavero, Daniel L Picchietti. Clinical efficacy and safety of intravenous ferric carboxymaltose treatment of pediatric restless legs syndrome and periodic limb movement disorder.
Sleep medicine.
2021 11; 87(?):114-118. doi:
10.1016/j.sleep.2021.08.030
. [PMID: 34562823] - Orhan Efe, Juan David Cala García, David Bruce Mount, Alice Marie Sheridan. Refractory hypophosphatemia following ferric carboxymaltose administration.
CEN case reports.
2021 11; 10(4):473-475. doi:
10.1007/s13730-021-00590-1
. [PMID: 33715107] - Moupriya Nag, Dibyajit Lahiri, Sayantani Garai, Dipro Mukherjee, Rina Rani Ray. Regulation of β-amylase synthesis: a brief overview.
Molecular biology reports.
2021 Sep; 48(9):6503-6511. doi:
10.1007/s11033-021-06613-5
. [PMID: 34379288] - Amália Ferreira, Thiago Cahú, Jinchuan Xu, Andreas Blennow, Ranilson Bezerra. A highly stable raw starch digesting α-amylase from Nile tilapia (Oreochromis niloticus) viscera.
Food chemistry.
2021 Aug; 354(?):129513. doi:
10.1016/j.foodchem.2021.129513
. [PMID: 33765464] - Sant-Rayn Pasricha, Michael Gilbertson, Tishya Indran, Ashwini Bennett, Matthew van Dam, Elizabeth Coughlin, Anouk Dev, Sanjeev Chunilal, Stephen Opat. Safety of rapid injection of undiluted ferric carboxymaltose to patients with iron-deficiency anaemia: a Phase II single-arm study.
Internal medicine journal.
2021 Aug; 51(8):1304-1311. doi:
10.1111/imj.15195
. [PMID: 33462917] - Tao Tian, Guo-Ying Chen, Hao Zhang, Feng-Qing Yang. Personal Glucose Meter for α-Glucosidase Inhibitor Screening Based on the Hydrolysis of Maltose.
Molecules (Basel, Switzerland).
2021 Jul; 26(15):. doi:
10.3390/molecules26154638
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The Lancet. Haematology.
2021 Jul; 8(7):e503-e512. doi:
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Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.
2021 07; 53(7):830-834. doi:
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The Plant journal : for cell and molecular biology.
2021 06; 106(5):1431-1442. doi:
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Medicine.
2021 May; 100(20):e24571. doi:
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British journal of clinical pharmacology.
2021 05; 87(5):2256-2273. doi:
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American journal of hematology.
2021 05; 96(5):606-616. doi:
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Scientific reports.
2021 04; 11(1):7463. doi:
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Journal of clinical pharmacology.
2021 04; 61(4):515-521. doi:
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European journal of heart failure.
2021 04; 23(4):593-597. doi:
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Mikrochimica acta.
2021 03; 188(4):142. doi:
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Langmuir : the ACS journal of surfaces and colloids.
2021 02; 37(6):2111-2122. doi:
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Sleep.
2021 02; 44(2):. doi:
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Nutrients.
2021 Feb; 13(2):. doi:
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Food chemistry.
2021 Feb; 337(?):127977. doi:
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Journal of separation science.
2021 Feb; 44(3):709-716. doi:
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The Annals of pharmacotherapy.
2021 02; 55(2):222-229. doi:
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Lancet (London, England).
2020 12; 396(10266):1895-1904. doi:
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Clinical nutrition (Edinburgh, Scotland).
2020 12; 39(12):3779-3785. doi:
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Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.
2020 Dec; 24(6):642-647. doi:
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Bone.
2020 12; 141(?):115559. doi:
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Molecules (Basel, Switzerland).
2020 Nov; 25(21):. doi:
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The National medical journal of India.
2020 Nov; 33(6):324-328. doi:
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Sleep medicine.
2020 11; 75(?):81-87. doi:
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International journal of clinical practice.
2020 Oct; 74(10):e13584. doi:
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Molecular medicine reports.
2020 Oct; 22(4):3525-3532. doi:
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Food & function.
2020 Aug; 11(8):7037-7047. doi:
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Journal of proteomics.
2020 08; 225(?):103845. doi:
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Microbiology (Reading, England).
2020 08; 166(8):759-776. doi:
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BMC medicine.
2020 07; 18(1):178. doi:
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Obesity surgery.
2020 07; 30(7):2659-2666. doi:
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BMC gastroenterology.
2020 Jun; 20(1):183. doi:
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A&A practice.
2020 Jun; 14(8):e01234. doi:
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BMJ open respiratory research.
2020 06; 7(1):. doi:
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Journal of sports science & medicine.
2020 06; 19(2):282-288. doi:
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Indian journal of public health.
2020 Apr; 64(2):168-172. doi:
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Food research international (Ottawa, Ont.).
2020 04; 130(?):108844. doi:
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Journal of chromatography. A.
2020 Mar; 1615(?):460754. doi:
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The British journal of nutrition.
2020 03; 123(6):619-626. doi:
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Food & function.
2020 Feb; 11(2):1672-1683. doi:
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Carbohydrate polymers.
2020 Feb; 230(?):115611. doi:
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JAMA.
2020 02; 323(5):432-443. doi:
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Biochimica et biophysica acta. Biomembranes.
2020 02; 1862(2):183113. doi:
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Clinical therapeutics.
2020 02; 42(2):276-285. doi:
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Biochimica et biophysica acta. Biomembranes.
2020 02; 1862(2):183125. doi:
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The Plant cell.
2020 02; 32(2):449-469. doi:
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BioMed research international.
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Journal of insect physiology.
2020 01; 120(?):103969. doi:
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Nature reviews. Nephrology.
2020 01; 16(1):7-19. doi:
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Journal of the American Chemical Society.
2019 12; 141(50):19677-19687. doi:
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Analytica chimica acta.
2019 Dec; 1088(?):63-71. doi:
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The Journal of clinical investigation.
2019 12; 130(1):491-506. doi:
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European journal of heart failure.
2019 12; 21(12):1651-1658. doi:
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Advances in therapy.
2019 11; 36(11):3253-3264. doi:
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International journal of environmental research and public health.
2019 10; 16(20):. doi:
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Clinical journal of the American Society of Nephrology : CJASN.
2019 10; 14(10):1528-1530. doi:
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Food chemistry.
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Journal of the science of food and agriculture.
2019 Sep; 99(12):5586-5593. doi:
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ESC heart failure.
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Basic & clinical pharmacology & toxicology.
2019 Aug; 125(2):133-141. doi:
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Journal of clinical pharmacology.
2019 07; 59(7):947-957. doi:
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Nephrologie & therapeutique.
2019 Apr; 15(2):104-109. doi:
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Food chemistry.
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Food chemistry.
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BMC nephrology.
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Journal of agricultural and food chemistry.
2019 Feb; 67(7):2012-2019. doi:
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Marine biotechnology (New York, N.Y.).
2019 Feb; 21(1):99-110. doi:
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[Rinsho ketsueki] The Japanese journal of clinical hematology.
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