Acarbose Hydrate - Moligand™, ≥98% , Inhibitor of amylase alpha 2A;Inhibitor of maltase-glucoamylase, CAS No.56180-94-0, Inhibitor of amylase alpha 2A;Inhibitor of maltase-glucoamylase

CAS: 56180-94-0 Cat. No.: A129816 Peso molecular: 645.61(as Anhydrous) Número EC: 260-030-7
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
Bay-g 5421 | BAY g 5421 | Bay g 5421 | BRD-A16444946-001-07-1 | MLS001424056 | AB00639959-06 | HMS2093I22 | MFCD00869592 | Prandase; | SR-01000759407 | SBI-0206777.P001 | acarbose | MD-0230 | SR-01000759407-4 | Acarbose; O-4,6-Dideoxy-4-[[(1S,4R,5S,6S)-4,
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
A129816-250mg
4

16,90US$

25,90US$
Guardar 9,00 US$ (34.75%)
1g
A129816-1g
5

32,90US$

49,90US$
Guardar 17,00 US$ (34.07%)
5g
A129816-5g
2

110,90US$

166,90US$
Guardar 56,00 US$ (33.55%)
10g
A129816-10g
1

199,90US$

299,90US$
Guardar 100,00 US$ (33.34%)
25g
A129816-25g
1

385,90US$

578,90US$
Guardar 193,00 US$ (33.34%)
100g
A129816-100g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.349,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 196 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Acarbose, also known as BAY g 5421, is an α-glucosidase inhibitor that prevents absorption of sucrose and maltose. This compound has been found to delay digestion of complex disaccharides and carbohydrates. Further studies suggest that this compound can stimulate phosphorylase kinase (PhK) by binding to the glucoamylase-like domain new the amino termini and causing an alteration in the structure.
An α-glucosidase inhibitor


Application:

Acarbose, a derivitized maltotriose antidiabetic drug, is a reversible α-glucosidase inhibitor used in medical studies to control the effects of Type II diabetes. Acarbose is often used as a reference to which other α-glucosidase inhibitors are compared.

Specifications

Sinónimos
Bay-g 5421 | BAY g 5421 | Bay g 5421 | BRD-A16444946-001-07-1 | MLS001424056 | AB00639959-06 | HMS2093I22 | MFCD00869592 | Prandase; | SR-01000759407 | SBI-0206777.P001 | acarbose | MD-0230 | SR-01000759407-4 | Acarbose; O-4, 6-Dideoxy-4-[[(1S, 4R, 5S, 6S)-4,
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Potent α-glucosidase inhibitor (IC 50 = 11 nM). Orally active. Antidiabetic.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
INHIBITOR
Mecanismo de acción
Inhibitor of amylase alpha 2A;Inhibitor of maltase-glucoamylase
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488183332
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183332
Sonrisas canónicasCC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)NC4C=C(C(C(C4O)O)O)CO
IUPAC Name(3R,4R,5S,6R)-5-[(2R,3R,4R,5S,6R)-5-[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino]oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol
InChIKeyXUFXOAAUWZOOIT-UGEKTDRHSA-N
INCHI1S/C25H43NO18/c1-6-11(26-8-2-7(3-27)12(30)15(33)13(8)31)14(32)19(37)24(40-6)43-22-10(5-29)42-25(20(38)17(22)35)44-21-9(4-28)41-23(39)18(36)16(21)34/h2,6,8-39H,3-5H2,1H3/t6-,8+,9-,10-,11-,12-,13+,14+,15+,16-,17-,18-,19-,20-,21-,22-,23?,24-,25-/m1/s1
Isómeros SMILES C[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](O[C@@H]([C@@H]([C@H]2O)O)O[C@@H]3[C@H](OC([C@@H]([C@H]3O)O)O)CO)CO)O)O)N[C@H]4C=C([C@H]([C@@H]([C@H]4O)O)O)CO
RTECS LZ7153000
Peso molecular 645.61(as Anhydrous)
Reaxy-Rn 24713589
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24713589&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides - Aminoglycosides
Direct ParentAminocyclitol glycosides
Alternative Parents Oligosaccharides  O-glycosyl compounds  Oxanes  Cyclitols and derivatives  Secondary alcohols  Hemiacetals  1,2-aminoalcohols  Polyols  Oxacyclic compounds  Dialkylamines  Acetals  Primary alcohols  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Oligosaccharide - Amino cyclitol glycoside - Glycosyl compound - O-glycosyl compound - Cyclitol or derivatives - Oxane - 1,2-aminoalcohol - Hemiacetal - Secondary alcohol - Secondary amine - Organoheterocyclic compound - Acetal - Oxacycle - Secondary aliphatic amine - Polyol - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.
External Descriptors tetrasaccharide derivative
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
MGAM Tclin Maltase-glucoamylase, intestinal (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
AMY2A Tclin Pancreatic alpha-amylase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

41 results found

Lot NumberCertificate TypeFechaArticulo
G2411233Certificate of AnalysisApr 07, 2026 A129816
G2411232Certificate of AnalysisApr 07, 2026 A129816
B2603211Certificate of AnalysisJan 20, 2026 A129816
B2603213Certificate of AnalysisJan 20, 2026 A129816
B2603214Certificate of AnalysisJan 20, 2026 A129816
B2603216Certificate of AnalysisJan 20, 2026 A129816
B2603217Certificate of AnalysisJan 20, 2026 A129816
B2603207Certificate of AnalysisJan 20, 2026 A129816
J2307076Certificate of AnalysisJul 15, 2025 A129816
I2318159Certificate of AnalysisJul 15, 2025 A129816
H2321101Certificate of AnalysisJun 09, 2025 A129816
L2515035Certificate of AnalysisApr 18, 2025 A129816
D2530096Certificate of AnalysisApr 18, 2025 A129816
D2530095Certificate of AnalysisApr 18, 2025 A129816
D2530087Certificate of AnalysisApr 18, 2025 A129816
D2530085Certificate of AnalysisApr 18, 2025 A129816
D2530086Certificate of AnalysisApr 18, 2025 A129816
C2304160Certificate of AnalysisDec 06, 2024 A129816
C2304157Certificate of AnalysisDec 06, 2024 A129816
K2422281Certificate of AnalysisNov 09, 2024 A129816
K2422280Certificate of AnalysisNov 09, 2024 A129816
K2422279Certificate of AnalysisNov 09, 2024 A129816
I2424124Certificate of AnalysisSep 05, 2024 A129816
I2424123Certificate of AnalysisSep 05, 2024 A129816
I2424122Certificate of AnalysisSep 05, 2024 A129816
I2424121Certificate of AnalysisSep 05, 2024 A129816
G2411242Certificate of AnalysisJun 14, 2024 A129816
G2411243Certificate of AnalysisJun 14, 2024 A129816
G2411239Certificate of AnalysisJun 14, 2024 A129816
G2411238Certificate of AnalysisJun 14, 2024 A129816
E2414008Certificate of AnalysisJan 05, 2024 A129816
E2113058Certificate of AnalysisFeb 13, 2023 A129816
E2113057Certificate of AnalysisFeb 13, 2023 A129816
E2113060Certificate of AnalysisFeb 13, 2023 A129816
C2223160Certificate of AnalysisFeb 18, 2022 A129816
C2223149Certificate of AnalysisFeb 18, 2022 A129816
C2223169Certificate of AnalysisFeb 18, 2022 A129816
E2420045Certificate of AnalysisFeb 18, 2022 A129816
C2223142Certificate of AnalysisFeb 18, 2022 A129816
D2310198Certificate of AnalysisFeb 18, 2022 A129816
C2223127Certificate of AnalysisFeb 18, 2022 A129816

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Propiedades químicas y físicas
SolubilidadSoluble in water (100 mM), DMSO (100 mM), and methanol.
Rotación específica [α]176° (C=1,H2O)
Peso molecular645.600 g/mol
XLogP3-8.500
Hydrogen Bond Donor Count14
Hydrogen Bond Acceptor Count19
Rotatable Bond Count9
Exact Mass645.248 Da
Monoisotopic Mass645.248 Da
Topological Polar Surface Area321.000 Ų
Heavy Atom Count44
Formal Charge0
Complexity962.000
Isotope Atom Count0
Defined Atom Stereocenter Count18
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Qu-Jing Luo, Wen-Chao Zhou, Xin-Yi Liu, Ya-Jie Li, Qing-Ling Xie, Bin Wang, Chao Liu, Wen-Mao Wang, Wei Wang, Xu-Dong Zhou.  (2023)  Chemical Constituents and α-Glucosidase Inhibitory, Antioxidant and Hepatoprotective Activities of Ampelopsis grossedentata.  MOLECULES,  28  (24): (7956).  [PMID:38138447] [10.3390/molecules28247956]
2. Hui-Ting Cao, Tiansheng Zhao, Wei Liu, Cai-Ying Xu, Yi-Jing Liao, Xi-Luan Yan, Xi Mai, Na Li.  (2023)  Smartphone-assisted ratiometric fluorescence sensor for sensitive and portable α-glucosidase activity detection and inhibitor screening.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.109723]
3. Si-Lu Wang, Jie Yu, Jian-Xi Song, Qing-Fan Meng, Zhuo-Rui Zhang, Gui-Quan Jiang.  (2023)  Isolation, purification, structural analysis and in vitro activity of polysaccharides from Amelanchier alnifolia Nutt..  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2023.12.002]
4. Kumaravel Kaliaperumal, Linyan Zhang, Liangliang Gao, Qin Xiong, Yan Liang, Yueming Jiang, Jun Zhang.  (2023)  Insight into the Inhibitory Mechanisms of Hesperidin on α-Glucosidase through Kinetics, Fluorescence Quenching, and Molecular Docking Studies.  Foods,  12  (22): (4142).  [PMID:38002199] [10.3390/foods12224142]
5. Yu Zheng, Ruifen Zhang, Fei Huang, Lai-Hoong Cheng, Liangxiong Xu, Xuchao Jia.  (2023)  α-Glucosidase inhibitors derived from black soybean and their inhibitory mechanisms.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2023.115502]
6. Gonglin Cai, Hangmeng Dong, Shoulong Liu, Weijie Wu, Hailong Yang.  (2023)  Comparative Evaluation of the Physiochemical Properties, and Antioxidant and Hypoglycemic Activities of Dendrobium officinale Leaves Processed Using Different Drying Techniques.  Antioxidants,  12  (11): (1911).  [PMID:38001764] [10.3390/antiox12111911]
7. Na Li, Baijian Feng, Yongguang Bi, Fansheng Kong, Zhong Wang, Shaofan Tan.  (2023)  Sulfobutyl ether cyclodextrin inclusion complexes containing tea polyphenols: Preparation, characterization, antioxidant activity, α-glucosidase inhibition, and in vitro release property.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2023.136686]
8. Zeng Xiang, Dai Huijia, Liu Bing, Wen Yao.  (2023)  Optimization of the extraction process and hypoglycemic activity of Tieguanyin tea polyphenols.  Biomass Conversion and Biorefinery,      [PMID:] [10.1007/s13399-023-04821-6]
9. Dan Yang, Xin-yu-yao Ding, Hai-Xia Xu, Yu-Xian Guo, Qing-Feng Zhang.  (2023)  Chemical profile of Roselle extract and its inhibitory activities on three digestive enzymes in vitro and in vivo.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37714233] [10.1016/j.ijbiomac.2023.126902]
10. Qianqian Feng, Wei Yang, Zhiyun Peng, Guangcheng Wang.  (2023)  Utilizing bio-affinity ultrafiltration combined with UHPLC Q-Exactive Plus Orbitrap HRMS to detect potential α-glucosidase inhibitors in Oxalis corniculate L..  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37625761] [10.1016/j.ijbiomac.2023.126490]
11. Yue-Hua Chen, Si-Yu Li, Dan Wang, Wei Yuan, Kun Xu, Jia-Wei Wang, Ting-Guo Kang, Hui Zhang.  (2023)  Combinatorics-based chemical characterization and bioactivity comparison of different parts of traditional Chinese medicinal plants through LC-Q-TOF-MS/MS, multivariate statistical analysis and bioassay: Marsdenia tenacissima as an example.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:37598457] [10.1016/j.jchromb.2023.123850]
12. Jianjin GUO, Lu BAI, Chi-Tang HO, Sen GUO, Naisheng BAI.  (2023)  Chemical characterization, multivariate analysis and in vitro bioactivity evaluation of the roots of Fraxinus mandshurica.  CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.cjac.2023.100303]
13. Qinhao Guan, Lihua Tang, Liangliang Zhang, Lixin Huang, Man Xu, Yuan Wang, Meng Zhang.  (2023)  Molecular insights into α-glucosidase inhibition and antiglycation properties affected by the galloyl moiety in (−)-epigallocatechin-3-gallate.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  103  (15): (7381-7392).  [PMID:37390299] [10.1002/jsfa.12818]
14. Tao Gao, Shuang Liu, Huang-yang Luo, Ren Wu, Rui Yan, Ling-zhi He, Qing-yu Nie, Hua-li Tang, Guiju Sun.  (2023)  Purification, structural identification, antioxidant activity, and inhibitory effects on digestive enzymes of α-glucan from Chuanminshen violaceum.  Journal of Functional Foods,      [PMID:] [10.1016/j.jff.2023.105536]
15. Yichen Yin, Shiwei Sun, Hui Wang, Mengru Guo, Zhizhou Li, Chaoyi Lv, Zhao Yang, Wei Wang.  (2023)  Mechanism of interaction between urolithin A and α-glucosidase: Analysis by inhibition kinetics, fluorescence spectroscopy, isothermal titration calorimetry and molecular docking.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2023.135567]
16. Huan Li, Jichen Yang, Mengfan Wang, Xiangzhao Ma, Xin Peng.  (2023)  Studies on the inhibition of α-glucosidase by biflavonoids and their interaction mechanisms.  FOOD CHEMISTRY,      [PMID:37054519] [10.1016/j.foodchem.2023.136113]
17. Run Yu, Yue Li, Dun Si, Shulei Yan, Jingjing Liu, Jinping Si, Xinfeng Zhang.  (2023)  Identification, quantitative and bioactivity analyses of aroma and alcohol-soluble components in flowers of Gardenia jasminoides and its variety during different drying processes.  FOOD CHEMISTRY,      [PMID:37060668] [10.1016/j.foodchem.2023.135846]
18. Yao Wen, Caimei Su.  (2023)  Optimization of Ultrasonic Assisted Extraction and Bioactivity of Ophiopogon japonicus Polysaccharides by Response Surface Methodology.  STARCH-STARKE,      [PMID:] [10.1002/star.202200213]
19. Wen Yao, Zeng Xiang, Tan Hongyu, Liu Bing.  (2023)  Optimization of extraction process of total flavonoids from Cortex Lycii and its biological activities.  Biomass Conversion and Biorefinery,      [PMID:] [10.1007/s13399-023-03768-y]
20. Shuang Qi, Bo Jiang, Caoxing Huang, Yongcan Jin.  (2023)  Dual Regulation of Sulfonated Lignin to Prevent and Treat Type 2 Diabetes Mellitus.  BIOMACROMOLECULES,      [PMID:36608216] [10.1021/acs.biomac.2c01267]
21. Xi Peng, Kai Liu, Xing Hu, Deming Gong, Guowen Zhang.  (2022)  Hesperetin-Cu(II) complex as potential α-amylase and α-glucosidase inhibitor: Inhibition mechanism and molecular docking.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:36603279] [10.1016/j.saa.2022.122301]
22. Huihui Liu, Chang Zheng, Ziliang Li, Xiaoyang Xia, Dan Jiang, Wen Wang, Ruiying Zhang, Xia Xiang.  (2022)  Inhibitory mechanism of phenolic compounds in rapeseed oil on α-amylase and α-glucosidase: Spectroscopy, molecular docking, and molecular dynamic simulation.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:36542921] [10.1016/j.saa.2022.122251]
23. Xiu-Qing Song, Lin-Lin Tian, Tao Ye, Hu Liu, Hua Zhang.  (2022)  Steroid glycosides from the roots of Marsdenia tenacissima.  PHYTOCHEMISTRY,      [PMID:36347308] [10.1016/j.phytochem.2022.113506]
24. Jing Lei, Wei Li, Meng-Xi Fu, An-Qi Wang, Ding-Tao Wu, Huan Guo, Yi-Chen Hu, Ren-You Gan, Liang Zou, Ying Liu.  (2022)  Pressurized hot water extraction, structural properties, biological effects, and in vitro microbial fermentation characteristics of sweet tea polysaccharide.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:36243163] [10.1016/j.ijbiomac.2022.10.094]
25. Shan-Shan Zhang, Yu-Fei Hou, Shao-Jing Liu, Sen Guo, Chi-Tang Ho, Nai-Sheng Bai.  (2022)  Exploring Active Ingredients, Beneficial Effects, and Potential Mechanism of Allium tenuissimum L. Flower for Treating T2DM Mice Based on Network Pharmacology and Gut Microbiota.  Nutrients,  14  (19): (3980).  [PMID:36235633] [10.3390/nu14193980]
26. Chen Shanji, Tian Danmei, Wei Jihua, Li Cong, Ma Yihan, Gou Xiaoshuang, Shen Yiran, Chen Mei, Zhang Sihao, Li Jia, Wu Bin, Tang Jinshan.  (2022)  Citrinin Derivatives From Penicillium Citrinum Y34 That Inhibit α-Glucosidase and ATP-Citrate Lyase.  Frontiers in Marine Science,      [PMID:] [10.3389/fmars.2022.961356]
27. Wei Liu, Liang Ma, Liping Zhang, Yuchan Chen, Qingbo Zhang, Haibo Zhang, Weimin Zhang, Changsheng Zhang, Wenjun Zhang.  (2022)  Two New Phenylhydrazone Derivatives from the Pearl River Estuary Sediment-Derived Streptomyces sp. SCSIO 40020.  Marine Drugs,  20  (7): (449).  [PMID:35877742] [10.3390/md20070449]
28. Jiahe Fan, Chaoyi Lv, Zhizhou Li, Mengru Guo, Yichen Yin, Hui Wang, Wei Wang, Shiwei Sun.  (2022)  α-Glucosidase inhibitory effect of an anthraquinonoid produced by Fusarium incarnatum GDZZ-G2.  JOURNAL OF BASIC MICROBIOLOGY,  62  (11): (1360-1370).  [PMID:35736630] [10.1002/jobm.202200166]
29. Xiaoli Wang, Jichen Yang, Huan Li, Se Shi, Xin Peng.  (2022)  Mechanistic study and synergistic effect on inhibition of α-amylase by structurally similar flavonoids.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2022.119485]
30. Peng-Bo Duan, Ping-Ting Xiao, Xing Yang, Jin-Hua Hao, Kai Li, E-Hu Liu.  (2022)  Screening of hypoglycemic components in Platycladi Cacumen by phytochemical investigation, spectrum-effect relationship, and chemometric methods.  JOURNAL OF SEPARATION SCIENCE,  45  (14): (2591-2602).  [PMID:35593082] [10.1002/jssc.202200221]
31. Xinyue Zhang, Rizwan-ur Rehman, Songxue Wang, Yanglin Ji, Jing Li, Suwen Liu, Hao Wang.  (2022)  Blue honeysuckle extracts retarded starch digestion by inhibiting glycosidases and changing the starch structure.  Food & Function,  13  (11): (6072-6088).  [PMID:35550649] [10.1039/D2FO00459C]
32. Jie Liu, Fang-Fang Wang, Zheng-Meng Jiang, E-Hu Liu.  (2022)  Identification of antidiabetic components in Uncariae Rammulus Cum Uncis based on phytochemical isolation and spectrum–effect relationship analysis.  PHYTOCHEMICAL ANALYSIS,  33  (5): (659-669).  [PMID:35261095] [10.1002/pca.3118]
33. Shan-Shan Zhang, Niu-Niu Zhang, Sen Guo, Shao-Jing Liu, Yu-Fei Hou, Shiming Li, Chi-Tang Ho, Nai-Sheng Bai.  (2022)  Glycosides and flavonoids from the extract of Pueraria thomsonii Benth leaf alleviate type 2 diabetes in high-fat diet plus streptozotocin-induced mice by modulating the gut microbiota.  Food & Function,  13  (7): (3931-3945).  [PMID:35289350] [10.1039/D1FO04170C]
34. Ying Zhang, Yanna Pan, Jiaqi Li, Zeng Zhang, Yanming He, Hongjie Yang, Ping Zhou.  (2022)  Inhibition on α-Glucosidase Activity and Non-Enzymatic Glycation by an Anti-Oxidative Proteoglycan from Ganoderma lucidum.  MOLECULES,  27  (5): (1457).  [PMID:35268560] [10.3390/molecules27051457]
35. Hui Wang, Xiaoli Kang, Shiwei Sun, Yichen Yin, Kun Jiang, Guodong Tang, Xinning Tang, Wei Wang.  (2022)  Discovery of pyrogallol thermal reaction products from a model process of roasting coffee beans as potent α-glucosidase inhibitors.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2022.101583]
36. De-Fu Hong, Gui-Lin Hu, Xing-Rong Peng, Xiao-Yuan Wang, Yan-Bing Wang, Abdulbaset Al-Romaima, Zhong-Rong Li, Ming-Hua Qiu.  (2022)  Unusual ent-Kaurane Diterpenes from the Coffea Cultivar S288 Coffee Beans and Molecular Docking to α-Glucosidase.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:35005957] [10.1021/acs.jafc.1c06524]
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38. Chen Yu, Zi-Yi Yu, Yi-Ting Wen, Wei-Ming Chai, Lin-Jun Wang, Mei-Zhen Lin.  (2021)  Omeprazole inhibits α-glucosidase activity and the formation of nonenzymatic glycation products: Activity and mechanism.  JOURNAL OF BIOSCIENCE AND BIOENGINEERING,      [PMID:34802943] [10.1016/j.jbiosc.2021.10.007]
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126. Kaigang An, Xin Li, Jia Chen, Shuang Zhang, Jing Xiao, Qing Wang, Hongdeng Qiu.  (2024)  Deep eutectic solvent-assisted synthesis of La–Ce hybrid nanorods for the colorimetric determination of tetracycline in foods.  Analytical Methods,  16  (22): (3551-3561).  [PMID:38780040] [10.1039/D4AY00412D]
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128. Yi-Long Ma, Zi-Tong Wang, Dong-Mei Yang, Zhi Li, Qian-Lan Wu, Xin Guo, Ya-Fang Shang, Kiran Thakur, Zhao-Jun Wei.  (2024)  Effect of processing and simulated digestion on phenolics, antioxidant and hypoglycemic potential of winter jujube.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2024.116944]
129. Hao Xie, Wenwen Li, Linghe Zhang, Nurmamat Eliyas.  (2024)  Effects of Chemical Modification on the Structure and Biological Activities of Polysaccharides Extracted from Inonotus Obliquus by Microwave.  CHEMISTRY & BIODIVERSITY,      [PMID:38888110] [10.1002/cbdv.202400783]
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135. Jianing Ren, Jing Dai, Yue Chen, Zhenzhen Wang, Ruyi Sha, Jianwei Mao, Yangchen Mao.  (2024)  Hypoglycemic Activity of Rice Resistant-Starch Metabolites: A Mechanistic Network Pharmacology and In Vitro Approach.  Metabolites,  14  (4): (224).  [PMID:38668351] [10.3390/metabo14040224]
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137. Zhengming Xu, Kseniya Hileuskaya, Aliaksandr Kraskouski, Yujiao Yang, Zhe Huang, Zhengang Zhao.  (2024)  Inhibition of α-glucosidase activity and intestinal glucose transport to assess in vivo anti-hyperglycemia potential of dodecyl-acylated phlorizin and polydatin derivatives.  Food & Function,      [PMID:38511466] [10.1039/D3FO05233H]
138. Hai-Xia Xu, Qiao-Ting Xu, Zhong-Ping Yin, Ji-Guang Chen, Qing-Feng Zhang.  (2024)  Inhibitory activity of luteolin on α-glucosidase and pancreatic lipase in vitro and in vivo.  INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1111/ijfs.17115]
139. Qin Zhou, Yishi Wei, Yijing Liao, Xing Hu, Deming Gong, Guowen Zhang.  (2024)  Inhibitory mechanism of α-glucosidase by liquiritigenin and its combined effect with acarbose: Multi-spectroscopic analyses and molecular docking simulation.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.105659]
140. Qianqian Feng, Wei Yang, Xue Ma, Zhiyun Peng, Guangcheng Wang.  (2024)  Investigation on the anti-α-glucosidase mechanism of aspergillus triazolate A from Oxalis corniculate L..  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39270911] [10.1016/j.ijbiomac.2024.135457]
141. Donghui Wu, Qilin Zhao, Bing Zhang, Xianqing Tang, Yushu Li, Jian Sun, Xiurong Yang.  (2024)  Iron-Doped Polymer Dots with Enhanced Fluorescence and Dual Enzyme Activity for Versatile Bioassays.  ANALYTICAL CHEMISTRY,      [PMID:38324754] [10.1021/acs.analchem.3c04514]
142. Jing Xie, Li Zhang, Yu-Ying Bai, Wen-Jing Wang, Xia Hu, Shijun Li, Yang Tian.  (2024)  Isolation and purification of polyphenols, hypoglycemic and hypolipidemic and active constituent analysis of walnut septum polyphenols.  FOOD CHEMISTRY,      [PMID:39637665] [10.1016/j.foodchem.2024.142287]
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145. Jun-li Lv, Wen-qing Lai, Lei Pang, Xiao-ying Zhang, Kai-yi Zheng, Qiang Zhang, Zhan-peng Lu, Zhi-sheng Wang, Fasihul Lisan, Xue-yang Wang, Lu-feng Hu, Ming-jie Deng.  (2024)  Mode of action underlying toxicity of Camptothecin to Spodoptera frugiperda (Lepidoptera) larvae.  JOURNAL OF ASIA-PACIFIC ENTOMOLOGY,      [PMID:] [10.1016/j.aspen.2024.102322]
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148. Zhaolin Zhang, Qin Ruan, Xiaoming Sun, Jianfeng Yuan.  (2024)  Optimization of Enzymolysis Modification Conditions of Dietary Fiber from Bayberry Pomace and Its Structural Characteristics and Physicochemical and Functional Properties.  MOLECULES,  29  (14): (3415).  [PMID:39064993] [10.3390/molecules29143415]
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150. Wen Yao, Chen Jiawen.  (2024)  Optimization of Ultrasound-Assisted Deep Eutectic Solvent Extraction, Characterization, and Bioactivities of Polysaccharide from Pericarpium Citri Reticulatae.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,      [PMID:38904917] [10.1007/s12010-024-04990-8]
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152. Yi Wang, Ruge Lin, Laiming Zhang, Suqing Lan, Xingqian Ye, Haibo Pan, Shiguo Chen.  (2024)  Oxygen influences in vitro assessment for phenolic compounds: Digestive stability, α-glucosidase inhibitory activity and bioavailability.  FOOD CHEMISTRY,      [PMID:39608122] [10.1016/j.foodchem.2024.142165]
153. Wanxian Wang, Yanfang Liu, Dian Liu, Han Zhou, Yan Li, Wenjie Yuan, Suowen Xu, Jixia Wang, Xinmiao Liang, Jianping Weng.  (2024)  Profiling of Antidiabetic Bioactive Flavonoid Compounds from an Edible Plant Kudzu (Pueraria lobata).  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:38976778] [10.1021/acs.jafc.4c02564]
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155. Chuling Liu, Li Cheng, Mingtian Yang, Zhengli He, Yanan Jia, Li Xu, Yuansong Zhang.  (2025)  Screening for Safe and Efficient Monascus Strains with Functions of Lowering Blood Lipids, Blood Glucose, and Blood Pressure.  Foods,  14  (5): (835).  [PMID:40077539] [10.3390/foods14050835]
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157. Li Zhao, Shuang Luo, Zhiyun Peng, Guangcheng Wang.  (2025)  Studies on the inhibition mechanism of α-glucosidase by kaempferide: Enzyme kinetic, multi-spectroscopy and molecular docking techniques.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39908884] [10.1016/j.ijbiomac.2025.140637]
158. Wenhao Zhou, Huixian Chen, Yinghan Tian, Jiachuan Lei, Jianqing Yu.  (2024)  Study on antioxidant and antidiabetic components of Cirsium setosum based on molecular networking.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.104774]
159. Yifeng Chen, Huan Yi, Siyi Pan.  (2024)  Study on the extraction of Phycocyanin and the impact of in vitro simulated digestion on its anti-diabetic ability.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.105211]
160. Xiaonan Zhang, Xiaocheng Zhuang, Manxin Chen, Jingrong Wang, Zhuoyu Liu, Daxiong Qiu, Jinna Wang, Yan Huang, Weina Li, Zhiwei Liu.  (2024)  Tannin Acid/Fe3+ Composite Film Filled with Essential Oil Extracted from Melaleuca bracteata F. Muell Leaves for the Preservation of Mango.  CHEMISTRY & BIODIVERSITY,      [PMID:39530337] [10.1002/cbdv.202402221]
161. Yan-Yun Liu, Zheng-Ao Li, Yu-Zheng Zhou, Sen-Lin Wang, Zong-Peng Chen, Si-Xu Liu, Peng Zhan, Ying-Jun Zhou, Zan-Xian Xia, Xu Deng.  (2025)  TCM theory-inspired discovery of DNJ-flavonoid conjugates as broad-spectrum anti-SARS-CoV-2 agents by primarily targeting ER-associated glycoprotein folding process.  EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:40168909] [10.1016/j.ejmech.2025.117582]
162. Zhou Jian-Feng, Xu Hai-Xia, Yin Zhong-Ping, Chen Ji-Guang, Zhang Qing-Feng.  (2024)  The combination effects of quercetin on starch and digestive enzymes reduce postprandial blood glucose in rats.  EUROPEAN FOOD RESEARCH AND TECHNOLOGY,      [PMID:] [10.1007/s00217-023-04455-y]
163. Te Yu, Yonggang Dai, Zifei Wang, Yang Gao, Qiong Wu.  (2025)  Ultrasound-induced modifications of Auricularia auricula polysaccharides: Implications for antioxidant and glucose-lowering activities.  Food Chemistry-X,      [PMID:39974537] [10.1016/j.fochx.2025.102209]
164. Jianjin Guo, Chi-Tang Ho, Naisheng Bai.  (2024)  Utilizing HPLC-DAD, multivariate analysis, molecular docking, and in vitro validation methods to investigate phenolic compounds with potential antidiabetic properties in Fraxinus mandshurica.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111771]
165. Xiangxing Meng, Rui Liu, Jiao Xie, Liwei Li, Yu Kai, Jianhui Liu, Ye Zhang, Hao Wang.  (2024)  Valuation of the significant hypoglycemic activity of black currant anthocyanin extract by both starch structure transformation and glycosidase activity inhibition.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38714278] [10.1016/j.ijbiomac.2024.132112]
166. Deli Zou, Lei Liu, Fangshen Liu, Dahong Li, Huiming Hua.  (2024)  α-Glucosidase Inhibitory Components from Garcinia pedunculata Fruits.  CHEMISTRY & BIODIVERSITY,      [PMID:38459792] [10.1002/cbdv.202400409]
167. Hong-Jiao Zhang, Li-Wei He, Ke-Min Dong, Song-Yuan Li, Can Luo, Jia-Qi Han, Rui Li.  (2024)  β-Cyclodextrin functionalized persistent luminecence nanoparticle for autofluorescence-free detection of α-glucosidase activity and its inhibitor.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.112211]
168. Xu Wenyi, Guan Yinghua, Tian Liping, Fu Yu, Zhang Yinghui, Liu Yanhong, Hu Yanfei, Zhao Bowen, Wu Chongming.  (2025)  Lacticaseibacillus paracasei Glu-07: A Promising Probiotic Candidate for the Management of Type 2 Diabetes Mellitus.  CURRENT MICROBIOLOGY,  82  (9): (1-18).  [PMID:40694135] [10.1007/s00284-025-04391-y]
169. Yue Zhu, Yuting Ai, Jianfu Zhou, Xiaozhuan Jia, Shuying Liu, Bo Zhu, Yimin Qin, Jianping Jiang, Zhenzhong Yang.  (2025)  Unveiling bioactive components in Sargassum fusiforme via phytochemical and biological evaluation: A heterogeneous information ensemble approach.  Chinese Herbal Medicines,      [PMID:41399786] [10.1016/j.chmed.2025.08.002]
170. Lihong Zhang, Shuang Zhao, Jingxuan Wang, Jiaxin Zhang, Tian Zheng, Jingyi Li, Chuangui Ma, Jingxin Liu.  (2025)  Enzymatic degradation, structural characterization, and in vitro antioxidant, hypoglycemic, and anti-inflammatory activities of Sanghuang vaninii polysaccharides.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40865830] [10.1016/j.ijbiomac.2025.147114]
171. Wang Feifei, Wang Xinling, Wang Yu, Zhang Yin, Liu Tianxiang, Sun Jian.  (2025)  In situ formation of fluorescent non-conjugated polymer dots for α-glucosidase activity assay and inhibitor screening.  MICROCHIMICA ACTA,  192  (9): (1-10).  [PMID:40779177] [10.1007/s00604-025-07417-1]
172. Yu Wang, Qilin Zhao, Qi Fang, Jian Sun, Yan Du, Haji Akber Aisa.  (2025)  A cascade nanoreactor based on metal azolate framework integrated natural enzyme for α-glucosidase activity assay and inhibitor screening.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40344727] [10.1016/j.jcis.2025.137764]
173. Jing Jing, Li Huizhen, Li Cheng, Xu Mengjie, Zhao Yana, Cui Jianlan, Zhang Zhijun.  (2025)  Physicochemical, rheological properties, and hypoglycemic activities of polysaccharides from Hemerocallis citrina Baroni leaves and stems.  Journal of Food Measurement and Characterization,      [PMID:] [10.1007/s11694-025-03287-6]
174. Chen Chen, Yi Wen, Xilei Wang, Hong Cheng, Jianqing Yu.  (2025)  Molecular networking-based discovery of components with antioxidant and α-glucosidase inhibitory activities in burdock root.  FOOD CHEMISTRY,      [PMID:40592091] [10.1016/j.foodchem.2025.145278]
175. Qiong Wu, Xinru Wu, Zifei Wang, Zhitong Cai, Yonggang Dai.  (2025)  Fermentation-synergized physical modification: Enhancing physicochemical properties and bioactivities of soluble dietary fiber from peanut shells.  Food Chemistry-X,      [PMID:40606749] [10.1016/j.fochx.2025.102667]
176. Wen Yao, Chen Geping.  (2025)  Optimization of ultrasound-assisted deep eutectic solvent extraction, characterization, and bioactivities of polysaccharide from the fruit of Rosa roxburghii Tratt.  Journal of Food Measurement and Characterization,      [PMID:] [10.1007/s11694-025-03424-1]
177. Fang He, Shenglan Su, Ruihan Song, Yan Li, Luyan Zou, Zongjun Li, Yu Xiao, Aixiang Hou, Ke Li, Yuanliang Wang.  (2025)  Elucidating Key Components and Mechanisms Underlying the Synergistic Anti-Type 2 Diabetes Effect of Morus alba L. and Siraitia grosvenorii Combination: An Integrated In Vitro Enzymology, Untargeted Metabolomics, and Network Pharmacology Approach.  Antioxidants,  14  (9): (1065).  [PMID:41008970] [10.3390/antiox14091065]
178. Changyong Cai, Yunlan Chen, Zhonghai Tang, Zhijian Tan.  (2025)  Thermo-responsive ionic liquids-mediated extraction of Rosa roxburghii Tratt polysaccharides.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.135441]
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