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Recent Advances in Synthetic α‐Glucosidase Inhibitors
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0470862092openalex-snapshot
International Textbook of Diabetes Mellitus
inferredcites →https://doi.org/10.1002/ange.200351002openalex-snapshot
Nitrogen Inversion as a Diastereomeric Relay in Azasugar Synthesis: The First Synthesis of Adenophorine
inferredcites →https://doi.org/10.1002/anie.200351002openalex-snapshot
Nitrogen Inversion as a Diastereomeric Relay in Azasugar Synthesis: The First Synthesis of Adenophorine
inferredcites →https://doi.org/10.1002/ejoc.201402521openalex-snapshot
Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ϵ‐Lactone, and Cyclitols from Biocatalytically Derived β‐Hydroxy Esters as Chiral Precursors
inferredcites →https://doi.org/10.1002/ejoc.201501453openalex-snapshot
Fluorinated Radicamine A and B: Synthesis and Glycosidase Inhibition
inferredcites →https://doi.org/10.1007/s00044-014-1293-5openalex-snapshot
Design, synthesis, and biological evaluation of quinazoline derivatives as α-glucosidase inhibitors
inferredcites →https://doi.org/10.1007/s00044-016-1614-yopenalex-snapshot
Syntheses, in vitro evaluation and molecular docking studies of 5-bromo-2-aryl benzimidazoles as α-glucosidase inhibitors
inferredcites →https://doi.org/10.1007/s00044-016-1700-1openalex-snapshot
Comparative enzyme inhibition study of 1-deazapurines
inferredcites →https://doi.org/10.1016/j.bioorg.2016.08.011openalex-snapshot
A simple and efficient synthesis of novel inhibitors of alpha-glucosidase based on benzimidazole skeleton and molecular docking studies
inferredcites →https://doi.org/10.1016/j.bmc.2011.01.052openalex-snapshot
Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2011.02.028openalex-snapshot
Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor
inferredcites →https://doi.org/10.1016/j.bmc.2012.09.006openalex-snapshot
Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor. Part 2
inferredcites →https://doi.org/10.1016/j.bmc.2013.05.055openalex-snapshot
C-(α-d-Glucopyranosyl)-phenyldiazomethanes—irreversible inhibitors of α-glucosidase
inferredcites →https://doi.org/10.1016/j.bmc.2013.06.002openalex-snapshot
Synthesis and α-glucosidase inhibitory activity evaluation of N-substituted aminomethyl-β-d-glucopyranosides
inferredcites →https://doi.org/10.1016/j.bmc.2014.01.038openalex-snapshot
Synthesis, nitric oxide release, and α-glucosidase inhibition of nitric oxide donating apigenin and chrysin derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2015.10.038openalex-snapshot
2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2016.08.024openalex-snapshot
Molecular docking studies and synthesis of novel bisbenzimidazole derivatives as inhibitors of α-glucosidase
inferredcites →https://doi.org/10.1016/j.bmcl.2010.06.059openalex-snapshot
Docking and SAR studies of salacinol derivatives as α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2010.11.112openalex-snapshot
The synthesis and biological evaluation of 1-C-alkyl-l-arabinoiminofuranoses, a novel class of α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2011.02.109openalex-snapshot
Biological evaluation of 3′-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3′ position in the side chain on the α-glucosidase inhibitory activity
inferredcites →https://doi.org/10.1016/j.bmcl.2014.09.064openalex-snapshot
Amine-linked diquercitols as new α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2015.05.016openalex-snapshot
Discovery of xanthine oxidase inhibitors and/or α-glucosidase inhibitors by carboxyalkyl derivatization based on the flavonoid of apigenin
inferredcites →https://doi.org/10.1016/j.bmcl.2015.08.059openalex-snapshot
Synthesis, α-glucosidase inhibitory and molecular docking studies of prenylated and geranylated flavones, isoflavones and chalcones
inferredcites →https://doi.org/10.1016/j.carres.2011.12.026openalex-snapshot
Synthesis of 1,2,3-triazole glycoconjugates as inhibitors of α-glucosidases
inferredcites →https://doi.org/10.1016/j.carres.2014.06.015openalex-snapshot
Synthesis and evaluation of α-, β-glucosidase inhibition of 1-N-carboxamide-1-azafagomines and 5-epi-1-azafagomines
inferredcites →https://doi.org/10.1016/j.carres.2015.04.005openalex-snapshot
Synthesis of novel poly-hydroxyl functionalized acridine derivatives as inhibitors of α-Glucosidase and α-Amylase
inferredcites →https://doi.org/10.1016/j.ejmech.2011.06.003openalex-snapshot
Toward potent α-glucosidase inhibitors based on xanthones: A closer look into the structure–activity correlations
inferredcites →https://doi.org/10.1016/j.ejmech.2013.01.036openalex-snapshot
Fungal transformation of cedryl acetate and α-glucosidase inhibition assay, quantum mechanical calculations and molecular docking studies of its metabolites
inferredcites →https://doi.org/10.1016/j.ejmech.2013.05.047openalex-snapshot
Quercitylcinnamates, a new series of antidiabetic bioconjugates possessing α-glucosidase inhibition and antioxidant
inferredcites →https://doi.org/10.1016/j.ejmech.2014.04.018openalex-snapshot
Dual inhibition of the α-glucosidase and butyrylcholinesterase studied by Molecular Field Topology Analysis
inferredcites →https://doi.org/10.1016/j.ejmech.2015.10.017openalex-snapshot
Synthesis of novel flavone hydrazones: In-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies
inferredcites →https://doi.org/10.1016/j.ejmech.2016.01.029openalex-snapshot
Design, synthesis and biological evaluation of 3′-benzylated analogs of 3′-epi-neoponkoranol as potent α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.153openalex-snapshot
(+)-proto-Quercitol, a natural versatile chiral building block for the synthesis of the α-glucosidase inhibitors, 5-amino-1,2,3,4-cyclohexanetetrols
inferredcites →https://doi.org/10.1016/j.tetlet.2010.10.173openalex-snapshot
4-C-Me-DAB and 4-C-Me-LAB—enantiomeric alkyl-branched pyrrolidine iminosugars—are specific and potent α-glucosidase inhibitors; acetone as the sole protecting group
inferredcites →https://doi.org/10.1016/j.tetlet.2013.08.022openalex-snapshot
Synthesis and biological evaluation of carbohydrate appended hydrazinocyclopentenes with potent glycation and α-glucosidase inhibition activities
inferredcites →https://doi.org/10.1016/j.tetlet.2013.09.044openalex-snapshot
Synthetic study on neoponkoranol and its side chain epimer as potent α-glucosidase inhibitors, optimization of protecting group
inferredcites →https://doi.org/10.1016/j.tetlet.2013.11.110openalex-snapshot
Synthesis of novel zerumbone derivatives via regioselective palladium catalyzed decarboxylative coupling reaction: a new class of α-glucosidase inhibitors
inferredcites →https://doi.org/10.1016/s1056-8727(01)00148-9openalex-snapshot
Secretion of GIP in responders to acarbose in obese Type 2(NIDDM) patients
inferredcites →https://doi.org/10.1021/acs.joc.5b00133openalex-snapshot
Synthesis and Evaluation of Hydroxymethylaminocyclitols as Glycosidase Inhibitors
inferredcites →https://doi.org/10.1021/acs.joc.5b00342openalex-snapshot
Design and Synthesis of Labystegines, Hybrid Iminosugars from LAB and Calystegine, as Inhibitors of Intestinal α-Glucosidases: Binding Conformation and Interaction for ntSI
inferredcites →https://doi.org/10.1021/acs.joc.5b00571openalex-snapshot
Fluorinated and Conformationally Fixed Derivatives of l -HomoDMDP: Synthesis and Glycosidase Inhibition
inferredcites →https://doi.org/10.1021/acs.orglett.5b01505openalex-snapshot
Hydroxymethyl-Branched Polyhydroxylated Indolizidines: Novel Selective α-Glucosidase Inhibitors
inferredcites →https://doi.org/10.1021/jo3009534openalex-snapshot
α-Geminal Dihydroxymethyl Piperidine and Pyrrolidine Iminosugars: Synthesis, Conformational Analysis, Glycosidase Inhibitory Activity, and Molecular Docking Studies
inferredcites →https://doi.org/10.1021/jo4005487openalex-snapshot
C-Branched Iminosugars: α-Glucosidase Inhibition by Enantiomers of isoDMDP, isoDGDP, and isoDAB– l -isoDMDP Compared to Miglitol and Miglustat
inferredcites →https://doi.org/10.1021/jo4010553openalex-snapshot
Total Synthesis and Glycosidase Inhibition of Broussonetine I and J2
inferredcites →https://doi.org/10.1038/161707a0openalex-snapshot
Nature of Forces between Large Molecules of Biological Interest*
inferredcites →https://doi.org/10.1039/c2cc34144aopenalex-snapshot
In silico design, synthesis and evaluation of 3′-O-benzylated analogs of salacinol, a potent α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine “Salacia”
inferredcites →https://doi.org/10.1039/c2ob25943eopenalex-snapshot
Chemoenzymatic synthesis, structural study and biological activity of novel indolizidine and quinolizidine iminocyclitols
inferredcites →https://doi.org/10.1046/j.1463-1326.2002.00219.xopenalex-snapshot
The effects of miglitol on glucagon‐like peptide‐1 secretion and appetite sensations in obese type 2 diabetics
inferredcites →https://doi.org/10.1046/j.1464-5491.2000.00309.xopenalex-snapshot
Socio‐economic status, obesity and prevalence of Type 1 and Type 2 diabetes mellitus
inferredcites →https://doi.org/10.1074/jbc.m112.351858openalex-snapshot
Modulation of Starch Digestion for Slow Glucose Release through “Toggling” of Activities of Mucosal α-Glucosidases
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a009728openalex-snapshot
Estimating Prevalence of Type 1 and Type 2 Diabetes in a Population of African Americans with Diabetes Mellitus
inferredcites →https://doi.org/10.1111/dme.12791openalex-snapshot
Current prevalence of Type 1 and Type 2 diabetes in adults and children in the UK
inferredcites →https://doi.org/10.1111/j.1365-2362.1994.tb02418.xopenalex-snapshot
Significance of testing platelet functions in vitro
inferredcites →https://doi.org/10.1128/jvi.75.19.8987-8998.2001openalex-snapshot
Study of the Mechanism of Antiviral Action of Iminosugar Derivatives against Bovine Viral Diarrhea Virus
inferredcites →https://doi.org/10.1271/bbb.61.1233openalex-snapshot
Molecular Mechanism inα-Glucosidase and Glucoamylase
inferredcites →https://doi.org/10.1530/acta.0.1120361openalex-snapshot
Effects of Acarbose on the relationship between changes in GIP and insulin responses to meals in normal subjects
inferredcites →https://doi.org/10.2337/diacare.28.11.2613openalex-snapshot
Incidence of Type 1 and Type 2 Diabetes in Adults Aged 30–49 Years
inferredcites →https://doi.org/10.3109/14756366.2012.727812openalex-snapshot
Pyrimidine-fused heterocycle derivatives as a novel class of inhibitors for α-glucosidase
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ardp.202200421openalex-snapshot
Pyrazole scaffold‐based derivatives: A glimpse of α‐glucosidase inhibitory activity, SAR, and route of synthesis
inferred← citeshttps://doi.org/10.1002/asia.201900203openalex-snapshot
2‐Phenylquinoline–Sugar Hybrids as Photoswitchable α‐Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.1002/cbdv.202502336openalex-snapshot
Antioxidant, Antidiabetic, and Antiobesity Properties of Stachys cretica subsp. anatolica and Its LC–MS/MS Analysis: In Vitro and In Silico Studies
inferred← citeshttps://doi.org/10.1002/cbdv.202502599openalex-snapshot
Comparative Metabolomic Profiling and Antihyperglycemic Activity of Artabotrys hexapetalus and Artabotrys siamensis Leaf Extracts: In Vitro and In Silico Studies
inferred← citeshttps://doi.org/10.1002/cmdc.202500263openalex-snapshot
Adamantane‐Appended 1,2,3‐Triazole Hybrids: Synthesis and α‐Glucosidase Inhibition Studies through Experimental and In Silico Approach
inferred← citeshttps://doi.org/10.1002/jbm.a.37213openalex-snapshot
Development and evaluation of 1‐deoxynojirimycin sustained‐release delivery system: In vitro and in vivo characterization studies
inferred← citeshttps://doi.org/10.1002/open.202400014openalex-snapshot
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline–pyrazolopyrimidine hybrids and Quinoline‐4‐Arylamines
inferred← citeshttps://doi.org/10.1002/ps.5322openalex-snapshot
From synthetic control to natural products: a focus on N‐heterocycles
inferred← citeshttps://doi.org/10.1002/slct.202001657openalex-snapshot
Screening of α‐Glucosidase Inhibitors from Houttuynia cordata and Evaluation of the Binding Mechanisms
inferred← citeshttps://doi.org/10.1002/slct.202102119openalex-snapshot
Synthesis of New Valinol‐Derived Sultam Triazoles as α ‐Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.1002/slct.202405463openalex-snapshot
Dihydropyrimidinone Based Chromones as New α‐Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.1002/vjch.202400186openalex-snapshot
Bile acids: Can the position of hydroxyl substitution influence antidiabetic potency?
inferred← citeshttps://doi.org/10.1007/5584_2020_516openalex-snapshot
Glucose Lowering Treatment Modalities of Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.1007/s00044-021-02814-6openalex-snapshot
Design, synthesis, in vitro evaluation, and docking studies on ibuprofen derived 1,3,4-oxadiazole derivatives as dual α-glucosidase and urease inhibitors
inferred← citeshttps://doi.org/10.1007/s00044-024-03314-zopenalex-snapshot
Benzothiazole derivatives as effective α-glucosidase inhibitors: an insight study of structure-activity relationships and molecular targets
inferred← citeshttps://doi.org/10.1007/s00044-026-03563-0openalex-snapshot
Synthesis and structure–activity relationship studies of 1,2,4-triazole–benzoxazepine hybrids as α-glucosidase inhibitors: molecular docking and biological evaluation
inferred← citeshttps://doi.org/10.1007/s10719-020-09955-7openalex-snapshot
New approach to prepare fluorogenic branched dextrins for assaying glycogen debranching enzyme
inferred← citeshttps://doi.org/10.1007/s10904-024-03233-xopenalex-snapshot
Biochemical Characterization and Green Synthesis of Silver Nanoparticles (AgNPs) from Costus spicatus for Potential Anti-Diabetic Target in Streptozocin (STZ) Induced Diabetic Rats
inferred← citeshttps://doi.org/10.1007/s11030-020-10137-8openalex-snapshot
Synthesis of 4-alkylaminoimidazo[1,2-a]pyridines linked to carbamate moiety as potent α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1007/s11030-024-10831-xopenalex-snapshot
Exploring chalcone-sulfonyl piperazine hybrids as anti-diabetes candidates: design, synthesis, biological evaluation, and molecular docking study
inferred← citeshttps://doi.org/10.1007/s11033-021-06294-0openalex-snapshot
Exploring the recent molecular targets for diabetes and associated complications
inferred← citeshttps://doi.org/10.1016/b978-0-08-102922-0.00005-5openalex-snapshot
Current pharmacotherapy options for type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.ab.2019.113567openalex-snapshot
Validation of the ADVIA Centaur® XP system for the determination of insulin and its application
inferred← citeshttps://doi.org/10.1016/j.arabjc.2021.103651openalex-snapshot
Dicyanoanilines as potential and dual inhibitors of α-amylase and α-glucosidase enzymes: Synthesis, characterization, in vitro, in silico, and kinetics studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103128openalex-snapshot
Synthesis, in-vitro α-glucosidase inhibition, antioxidant, in-vivo antidiabetic and molecular docking studies of pyrrolidine-2,5-dione and thiazolidine-2,4-dione derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103945openalex-snapshot
Benzofuran-selenadiazole hybrids as novel α-glucosidase and cyclooxygenase-2 inhibitors with antioxidant and cytotoxic properties
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105073openalex-snapshot
A facile approach synthesis of benzoylaryl benzimidazole as potential α-amylase and α-glucosidase inhibitor with antioxidant activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105506openalex-snapshot
Synthesis of new clioquinol derivatives as potent α-glucosidase inhibitors; molecular docking, kinetic and structure–activity relationship studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106028openalex-snapshot
Flavone-1,2,3-triazole derivatives as potential α-glucosidase inhibitors: Synthesis, enzyme inhibition, kinetic analysis and molecular docking study
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106298openalex-snapshot
2,5-Disubstituted furan derivatives containing imidazole, triazole or tetrazole moiety as potent α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106709openalex-snapshot
Arylureidoaurones: Synthesis, in vitro α-glucosidase, and α-amylase inhibition activity
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110185openalex-snapshot
Effects of Bidens gardneri Baker leaves aqueous extract in glucose homeostasis of rats
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.127979openalex-snapshot
Dibenzazepine-linked isoxazoles: New and potent class of α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.128449openalex-snapshot
Towards multi-target antidiabetic agents: In vitro and in vivo evaluation of 3,5-disubstituted indolin-2-one derivatives as novel α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129173openalex-snapshot
Synthesis and biological evaluation of 2,5-disubstituted furan derivatives containing 1,3-thiazole moiety as potential α‐glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.carres.2017.09.009openalex-snapshot
The convergent synthesis and anticancer activity of broussonetinines related analogues
inferred← citeshttps://doi.org/10.1016/j.carres.2023.108746openalex-snapshot
Synthesis and evaluation of ent-Conduramine C-1 derivatives as α-glucosidase inhibitors via CSI-mediated amination reaction
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.07.022openalex-snapshot
Adipocyte fatty acid binding protein 4 (FABP4) inhibitors. A comprehensive systematic review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.07.073openalex-snapshot
A comprehensive review on xanthone derivatives as α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.04.025openalex-snapshot
Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114230openalex-snapshot
Design, synthesis and glycosidase inhibition of C-4 branched LAB and DAB derivatives
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106479openalex-snapshot
Discovery of antioxidants and α-glycosidase inhibitors from an endophytic fungus Penicillium brefeldianum F4a
inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.137528openalex-snapshot
Bacuri (Platonia insignis Mart.): Nutritional values, volatile compounds, rheological properties, health benefits, and potential products
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e37467openalex-snapshot
A review on the in vitro and in vivo screening of α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2017.11.151openalex-snapshot
Potential of Potentilla inclinata and its polyphenolic compounds in α-glucosidase inhibition: Kinetics and interaction mechanism merged with docking simulations
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.01.189openalex-snapshot
Investigation the interaction between procyanidin dimer and α-amylase: Spectroscopic analyses and molecular docking simulation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.02.105openalex-snapshot
Investigation the interaction between procyanidin dimer and α-glucosidase: Spectroscopic analyses and molecular docking simulation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.10.018openalex-snapshot
Construction of Fe3O4@α-glucosidase magnetic nanoparticles for ligand fishing of α-glucosidase inhibitors from a natural tonic Epimedii Folium
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.130920openalex-snapshot
Understanding changes in holocellulose and lignin compounds in wooden structure of veneers: Molecular insights post hydrothermal treatment and aging
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2019.109364openalex-snapshot
Design, properties and applications of fluorinated and fluoroalkylated N-containing monosaccharides and their analogues
inferred← citeshttps://doi.org/10.1016/j.jmgm.2023.108447openalex-snapshot
Discovery of the new alpha-glucosidase inhibitor with therapeutic potential in type 2 diabetes mellitus by a novel high-throughput virtual screening and free energy evaluation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131768openalex-snapshot
Design and synthesis of new benzylidene-quinazolinone hybrids as potential anti-diabetic agents: In vitro α-glucosidase inhibition, and docking studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134339openalex-snapshot
Synthesis, in-vitro α-glucosidase inhibition and molecular docking studies of 1,3,4-thiadiazole-5,6-diphenyl-1,2,4-triazine hybrids: Potential leads in the search of new antidiabetic drugs
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.134954openalex-snapshot
Synthesis and molecular modeling studies of naphthazarin derivatives as novel selective inhibitors of α-glucosidase and α-amylase
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135115openalex-snapshot
Recent developments in synthetic α-glucosidase inhibitors: A comprehensive review with structural and molecular insight
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137714openalex-snapshot
Synthesis of benzimidazoles containing piperazine ring as potential therapeutic agents against diabetes mellitus and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140000openalex-snapshot
Insights into the role of potent thiadiazole based Schiff base derivatives in targeting type-II diabetes: A combine in-vitro and in-silico approaches
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.141057openalex-snapshot
Synthesis, in vitro and in silico evaluation of indole linked carbohydrazides and 1,3,4-oxadiazoles as new α-glycosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143612openalex-snapshot
Semi-synthesis, biological evaluation and molecular docking studies of novel Benzylidene-2,4-thiazolidinedione derivatives from natural maslinic acid
inferred← citeshttps://doi.org/10.1016/j.procbio.2019.01.011openalex-snapshot
Exploring the effect of salvianolic acid C on α-glucosidase: Inhibition kinetics, interaction mechanism and molecular modelling methods
inferred← citeshttps://doi.org/10.1016/j.procbio.2025.04.011openalex-snapshot
Structure-guided discovery of natural α-glucosidase inhibitors from food sources for blood sugar regulation
inferred← citeshttps://doi.org/10.1016/j.saa.2019.03.109openalex-snapshot
Integrated multi-spectroscopic and molecular modelling techniques to probe the interaction mechanism between salvianolic acid A and α‑glucosidase
inferred← citeshttps://doi.org/10.1017/s2040174418000545openalex-snapshot
Placental imprinted gene expression mediates the effects of maternal psychosocial stress during pregnancy on fetal growth
inferred← citeshttps://doi.org/10.1021/acs.biochem.8b00731openalex-snapshot
Studies with Guanidinium- and Amidinium-Based Inhibitors Suggest Minimal Stabilization of Allylic Carbocation Intermediates by Dehydrosqualene and Squalene Synthases
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00485openalex-snapshot
Diastereoselective Synthesis, Glycosidase Inhibition, and Docking Study of C-7-Fluorinated Casuarine and Australine Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02577openalex-snapshot
Total Synthesis and Biological Evaluation of Asterriquinol D Dimethyl Ether, Candidusin D, Kumbicins A–B, and Petromurins C–D as α-Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01869openalex-snapshot
Total Synthesis of Nocarterphenyls A-B and 2-Dehydroxymethylnocarterphenyl A, Formal Synthesis of Nocarterphenyl D, and Biological Evaluation of Nocarterphenyls as α-Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.1021/acsomega.0c03871openalex-snapshot
Discovery of Novel Coumarin Analogs against the α-Glucosidase Protein Target of Diabetes Mellitus: Pharmacophore-Based QSAR, Docking, and Molecular Dynamics Simulation Studies
inferred← citeshttps://doi.org/10.1021/acsomega.2c01469openalex-snapshot
Stereoselective Synthesis of Nojirimycin α-C-Glycosides from a Bicyclic Acyliminium Intermediate: A Convenient Entry to N,C-Biantennary Glycomimetics
inferred← citeshttps://doi.org/10.1021/acssynbio.2c00571openalex-snapshot
Exploring the Substrate Specificity of a Sugar Transporter with Biosensors and Cheminformatics
inferred← citeshttps://doi.org/10.1039/c8gc00987bopenalex-snapshot
Catalyst-free three-component synthesis of highly functionalized 2,3-dihydropyrroles
inferred← citeshttps://doi.org/10.1039/c8ra04772copenalex-snapshot
Exploring the interaction between Salvia miltiorrhiza and α-glucosidase: insights from computational analysis and experimental studies
inferred← citeshttps://doi.org/10.1039/c9fo02806dopenalex-snapshot
Exploring the structure–activity relationship and interaction mechanism of flavonoids and α-glucosidase based on experimental analysis and molecular docking studies
inferred← citeshttps://doi.org/10.1039/d2ob01772eopenalex-snapshot
Design, synthesis, spectroscopic characterization, computational analysis, and in vitro α-amylase and α-glucosidase evaluation of 3-aminopyridin-2(1 H )-one based novel monothiooxamides and 1,3,4-thiadiazoles
inferred← citeshttps://doi.org/10.1039/d2ra00067aopenalex-snapshot
A review on α-glucosidase inhibitory activity of first row transition metal complexes: a futuristic strategy for treatment of type 2 diabetes
inferred← citeshttps://doi.org/10.1039/d2ra02697jopenalex-snapshot
Heterocyclic compounds as a magic bullet for diabetes mellitus: a review
inferred← citeshttps://doi.org/10.1039/d3nj00889dopenalex-snapshot
Design, synthesis and evaluation of l -quebrachitol derivatives against α-glycosidase
inferred← citeshttps://doi.org/10.1039/d3ob00404jopenalex-snapshot
Design and synthesis of iso- allo -DNJ and l -isoDALDP derivatives: pursuit of potent and selective inhibitors of α-glucosidase
inferred← citeshttps://doi.org/10.1039/d3ra01790gopenalex-snapshot
Synthesis, ADMT prediction, and in vitro and in silico α-glucosidase inhibition evaluations of new quinoline–quinazolinone–thioacetamides
inferred← citeshttps://doi.org/10.1039/d3ra02916fopenalex-snapshot
Design, synthesis, in silico , and in vitro evaluation of benzylbenzimidazolone derivatives as potential drugs on α-glucosidase and glucokinase as pharmacological targets
inferred← citeshttps://doi.org/10.1039/d4nj02535kopenalex-snapshot
Synthesis and biological evaluation of β-lactams as potent antidiabetic agents
inferred← citeshttps://doi.org/10.1039/d4tb02466dopenalex-snapshot
Intrinsic fluorescence hydrogels for ON/OFF screening of antidiabetic drugs: assessing α-glucosidase inhibition by acarbose
inferred← citeshttps://doi.org/10.1039/d6ra05668gopenalex-snapshot
Discovery of 4-aminochalcone-based dual α-glucosidase and aldose reductase inhibitors: in vitro , in vivo , and in silico studies
inferred← citeshttps://doi.org/10.1080/07391102.2024.2427373openalex-snapshot
Design, synthesis, biological evaluation, and molecular modeling studies of some quinazolin-4(3 H )-one-benzenesulfonamide hybrids as potential α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1080/14756366.2017.1363743openalex-snapshot
New quinoxalinone inhibitors targeting secreted phospholipase A2 and α-glucosidase
inferred← citeshttps://doi.org/10.1080/14756366.2020.1826941openalex-snapshot
Synthesis,in vitroinhibitory activity, kinetic study and molecular docking of novelN-alkyl–deoxynojirimycin derivatives as potential α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1080/17568919.2026.2732256openalex-snapshot
Exploring the antidiabetic potential of DHA-salicylaldehyde-chalcone endowed 1,2,3-triazole hybrids: synthesis, α-glucosidase inhibition and molecular modeling studies
inferred← citeshttps://doi.org/10.1107/s205698902000701xopenalex-snapshot
1-Ethyl 2-methyl 3,4-bis(acetyloxy)pyrrolidine-1,2-dicarboxylate: crystal structure, Hirshfeld surface analysis and computational chemistry
inferred← citeshttps://doi.org/10.1111/cbdd.13805openalex-snapshot
Discovery of potent α‐glucosidase inhibitors through structure‐based virtual screening of an in‐house azole collection
inferred← citeshttps://doi.org/10.1111/cbdd.14614openalex-snapshot
Synthesis of Novel Soritin Sulfonamide Derivatives as Potential α‐Glucosidase Inhibitor and Their Molecular Docking Studies
inferred← citeshttps://doi.org/10.1155/bmri/5193886openalex-snapshot
Heterocycle‐Tethered Aurones: Synthesis and Evaluation of α ‐Glucosidase Inhibition
inferred← citeshttps://doi.org/10.1186/s13065-023-00973-8openalex-snapshot
Synthesis, α-Glucosidase inhibitory activity and docking studies of Novel Ethyl 1,2,3-triazol-4-ylmethylthio-5,6-diphenylpyridazine-4-carboxylate derivatives
inferred← citeshttps://doi.org/10.13057/biodiv/d220929openalex-snapshot
Polyphenol content and pharmacological activities of Capsicum frutescens and C. chinense genotypes
inferred← citeshttps://doi.org/10.1371/journal.pone.0220379openalex-snapshot
Triazoloquinazolines as a new class of potent α-glucosidase inhibitors: in vitro evaluation and docking study
inferred← citeshttps://doi.org/10.2147/dddt.s334325openalex-snapshot
New Insights of Anti-Hyperglycemic Agents and Traditional Chinese Medicine on Gut Microbiota in Type 2 Diabetes
inferred← citeshttps://doi.org/10.2174/0113892037287976231212104607openalex-snapshot
An Update on Dipeptidyl Peptidase-IV Inhibiting Peptides
inferred← citeshttps://doi.org/10.2174/0115680266299494240326083936openalex-snapshot
The Role of Selenium Nanoparticles in Addressing Diabetic Complications: A Comprehensive Study
inferred← citeshttps://doi.org/10.2174/0115733998261903230921102620openalex-snapshot
Novel Approaches for the Management of Type 2 Diabetes Mellitus: An Update
inferred← citeshttps://doi.org/10.2174/0929867324666171106162259openalex-snapshot
Spirolactones: Recent Advances in Natural Products, Bioactive Compounds and Synthetic Strategies
inferred← citeshttps://doi.org/10.2174/1570180817999201104125018openalex-snapshot
Design and Synthesis of Novel 5-Arylisoxazole-1,3,4-thiadiazole Hybrids as α-Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.2174/1573408018666220627114552openalex-snapshot
In Silico Design, Synthesis and Evaluation of Hydroxyxanthone Derivatives as Potential Anti-diabetic Agents Targeting α-glucosidase
inferred← citeshttps://doi.org/10.2174/1573409914666181022142553openalex-snapshot
Effects of Hydroxyl Group on the Interaction of Carboxylated Flavonoid Derivatives with S. Cerevisiae α-Glucosidase
inferred← citeshttps://doi.org/10.25073/2588-1132/vnumps.4334openalex-snapshot
Potent Natural Inhibitors of Alpha-Glucosidase and the Application of Aspergillus spp. in Diabetes type 2 Drugs: a Review
inferred← citeshttps://doi.org/10.33483/jfpau.1760832openalex-snapshot
QUINOXALINE DERIVATIVES AS -GLUCOSIDASE INHIBITORS: SYNTHESIS AND BIOLOGICAL EVALUATION
inferred← citeshttps://doi.org/10.3389/fchem.2021.639279openalex-snapshot
Discovery of New α-Glucosidase Inhibitors: Structure-Based Virtual Screening and Biological Evaluation
inferred← citeshttps://doi.org/10.3389/fchem.2022.927624openalex-snapshot
Responsive Fluorescent Coumarin–Cinnamic Acid Conjugates for α-Glucosidase Detection
inferred← citeshttps://doi.org/10.3389/fendo.2025.1575087openalex-snapshot
Effect of acarbose and vildagliptin on plasma trimethylamine N-oxide levels in patients with type 2 diabetes mellitus: a 6-month, two-arm randomized controlled trial
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1050869openalex-snapshot
Metabolites extracted from microorganisms as potential inhibitors of glycosidases (α-glucosidase and α-amylase): A review
inferred← citeshttps://doi.org/10.3389/fphar.2019.00777openalex-snapshot
Head-to-Head Comparison of the Hypoglycemic Efficacy and Safety Between Dipeptidyl Peptidase-4 Inhibitors and α-Glucosidase Inhibitors in Patients With Type 2 Diabetes Mellitus: A Meta-Analysis of Randomized Controlled Trials
inferred← citeshttps://doi.org/10.3390/antiox11030553openalex-snapshot
Potential Mechanisms of the Improvement of Glucose Homeostasis in Type 2 Diabetes by Pomegranate Juice
inferred← citeshttps://doi.org/10.3390/biom10030418openalex-snapshot
Synthesis, In Vitro Evaluation and Molecular Docking of the 5-Acetyl-2-aryl-6-hydroxybenzo[b]furans against Multiple Targets Linked to Type 2 Diabetes
inferred← citeshttps://doi.org/10.3390/futurepharmacol6010002openalex-snapshot
From Painkillers to Antidiabetics: Structural Modification of NSAID Scaffolds for Drug Repurposing
inferred← citeshttps://doi.org/10.3390/genes11101116openalex-snapshot
Identification of QTLs Controlling α-Glucosidase Inhibitory Activity in Pepper (Capsicum annuum L.) Leaf and Fruit Using Genotyping-by-Sequencing Analysis
inferred← citeshttps://doi.org/10.3390/ijms221810050openalex-snapshot
Effectiveness of Magnolol, a Lignan from Magnolia Bark, in Diabetes, Its Complications and Comorbidities—A Review
inferred← citeshttps://doi.org/10.3390/md21020104openalex-snapshot
Enzyme Inhibitors from Gorgonians and Soft Corals
inferred← citeshttps://doi.org/10.3390/molecules24203712openalex-snapshot
Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues
inferred← citeshttps://doi.org/10.3390/molecules24234340openalex-snapshot
Synthesis and Comparative Structure–Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants
inferred← citeshttps://doi.org/10.3390/molecules26195840openalex-snapshot
Fishing of α-Glucosidase’s Ligands from Aloe vera by α-Glucosidase Functionalized Magnetic Nanoparticles
inferred← citeshttps://doi.org/10.3390/molecules26237223openalex-snapshot
Pharmacological Chaperone Therapy for Pompe Disease
inferred← citeshttps://doi.org/10.3390/molecules27217376openalex-snapshot
Research Advances of Bioactive Sesquiterpenoids Isolated from Marine-Derived Aspergillus sp.
inferred← citeshttps://doi.org/10.3390/molecules28186641openalex-snapshot
Drug Discovery Based on Fluorine-Containing Glycomimetics
inferred← citeshttps://doi.org/10.3390/molecules29051179openalex-snapshot
Synthesis and Biological Evaluation of New Dihydrofuro[3,2-b]piperidine Derivatives as Potent α-Glucosidase Inhibitors
inferred← citeshttps://doi.org/10.3390/ph16101392openalex-snapshot
Synthesis and Biological Evaluation of Some New 3-Aryl-2-thioxo-2,3-dihydroquinazolin-4(1H)-ones and 3-Aryl-2-(benzylthio)quinazolin-4(3H)-ones as Antioxidants; COX-2, LDHA, α-Glucosidase and α-Amylase Inhibitors; and Anti-Colon Carcinoma and Apoptosis-Inducing Agents
inferred← citeshttps://doi.org/10.3390/ph16121677openalex-snapshot
Green Synthesis and Characterization of Silver Nanoparticles Using Azadirachta indica Seeds Extract: In Vitro and In Vivo Evaluation of Anti-Diabetic Activity
inferred← citeshttps://doi.org/10.3390/ph17030377openalex-snapshot
Synthesis, Computational Study, and In Vitro α-Glucosidase Inhibitory Action of 1,3,4-Thiadiazole Derivatives of 3-Aminopyridin-2(1H)-ones
inferred← citeshttps://doi.org/10.3390/pharmaceutics15020457openalex-snapshot
Synthesis, Molecular Docking, and Bioactivity Study of Novel Hybrid Benzimidazole Urea Derivatives: A Promising α-Amylase and α-Glucosidase Inhibitor Candidate with Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/plants9010002openalex-snapshot
Alpha Glucosidase Inhibitory Activities of Plants with Focus on Common Vegetables
inferred← citeshttps://doi.org/10.36899/japs.2024.3.0743openalex-snapshot
PHARMACOLOGICAL AND BIOLOGICAL EVALUATION OF METHANOL EXTRACTS OF SELECTED CHOLISTANI PLANTS
inferred← citeshttps://doi.org/10.3923/pjbs.2020.132.138openalex-snapshot
Hypoglycemic Potential of Supplementation with a Vegetable and Legume Juice Formula in Type 2 Diabetic Patients
inferred← citeshttps://doi.org/10.4155/fmc-2018-0141openalex-snapshot
3-Benzyl(phenethyl)-2-thioxobenzo[ g ]quinazolines as a New Class of Potent α-Glucosidase Inhibitors: Synthesis and Molecular Docking Study
inferred← citeshttps://doi.org/10.4155/fmc-2022-0289openalex-snapshot
Inhibition of α-glucosidase Enzyme By ‘click'-inspired Pharmacophore Framework 1,3,4-thiadiazole–1,2,3-triazole Hybrids
inferred← citeshttps://doi.org/10.48198/njpas/22.b07openalex-snapshot
Gas Chromatography-Mass Spectroscopic Profile, In vitro Antidiabetic and Radical Scavenging Potentials of Polyalthia longifolia leaf phenolic extract
inferred← citeshttps://doi.org/10.6084/m9.figshare.23583480openalex-snapshot
Additional file 1 of Synthesis, α-Glucosidase inhibitory activity and docking studies of Novel Ethyl 1,2,3-triazol-4-ylmethylthio-5,6-diphenylpyridazine-4-carboxylate derivatives
inferred← citeshttps://doi.org/10.7831/ras.10.0_206openalex-snapshot
Quality Aspects Related to Meat Analogue Based on Microbiology, Plants and Insects Protein
inferred← citeshttps://doi.org/10.7841/ksbbj.2023.38.3.177openalex-snapshot
Antioxidant and Anti-obesity Activities of Roasted Camellia japonica Leaves Extract
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