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Rapid screening and identification of α ‐glucosidase inhibitors from mulberry leaves using enzyme‐immobilized magnetic beads coupled with HPLC/MS and NMR
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Novel Benzoic Acid Derivatives Bearing Quinazolin‐4(3 H )‐one Ring: Synthesis, Characterization, and Inhibition Effects on α‐Glucosidase and α‐Amylase
inferred← citeshttps://doi.org/10.1002/slct.202204149openalex-snapshot
Investigation of The Effect of Acylthiourea Derivatives on Diabetes‐Associated Enzymes
inferred← citeshttps://doi.org/10.1002/slct.202204196openalex-snapshot
HPLC analysis, Phytochemical Content, and Biological Effects of Centaurea kilae Against Some Metabolic Enzymes: In Vitro and In Silico Studies
inferred← citeshttps://doi.org/10.1002/slct.202204578openalex-snapshot
Metal‐Free Synthesis via Intramolecular Cyclization, Enzyme Inhibition Properties and Molecular Docking of Novel Isoindolinones
inferred← citeshttps://doi.org/10.1002/slct.202300170openalex-snapshot
Isofraxidin: Antioxidant, Anti‐carbonic Anhydrase, Anti‐cholinesterase, Anti‐diabetic, and in Silico Properties
inferred← citeshttps://doi.org/10.1002/slct.202300241openalex-snapshot
Synthesis, Characterization, Bioactivity Impacts of New Anthranilic Acid Hydrazones Containing Aryl Sulfonate Moiety as Fenamate Isosteres
inferred← citeshttps://doi.org/10.1002/slct.202300319openalex-snapshot
((E)‐N′(3,5‐di‐tert‐butil‐2‐hedroxybenzilidene)‐2‐hydroxybenzohydrazide (H3sahz) 2 Copper (II) Complex: Synthesis, Crystal Structures, in silico Evaluations, and Enzymatic Inhibition
inferred← citeshttps://doi.org/10.1002/slct.202301158openalex-snapshot
Synthesis and Evaluation of Quinazolin‐4(3 H )‐one Derivatives as Multitarget Metabolic Enzyme Inhibitors: A Biochemistry‐Oriented Drug Design
inferred← citeshttps://doi.org/10.1002/slct.202303054openalex-snapshot
In Vitro and in Silico Studies of 3‐Hydroxyflavone‐Based Sulfonate Esters: Potent Acetylcholinesterase, Carbonic Anhydrase and α‐Glycosidase Inhibitors
inferred← citeshttps://doi.org/10.1002/slct.202404087openalex-snapshot
Exploring Benzo[ b ][1,4]Thiazine Derivatives: Multitarget Inhibition, Structure–Activity Relationship, Molecular Docking, and ADMET Analysis
inferred← citeshttps://doi.org/10.1002/slct.202404467openalex-snapshot
Investigation of the Effect of Gingerol on α‐Glycosidase Cholinesterases and Monoamine Oxidase Enzymes: Antioxidant Activity and In Silico Study
inferred← citeshttps://doi.org/10.1002/slct.202405991openalex-snapshot
Isatis glauca Aucher Ex Boiss. Subsp. Glauca (Indigo) Extracts as Enzyme Inhibitors: A Biochemical Study
inferred← citeshttps://doi.org/10.1002/slct.202501545openalex-snapshot
Chemical Characterization by Chromatography Techniques and Comprehensive Biological Activities of Artvin Bee Products
inferred← citeshttps://doi.org/10.1002/slct.202503301openalex-snapshot
Investigation of Phenolic‐Flavonoid Contents, Antioxidant Capacities, and Enzyme Inhibitory Properties of Papaver Triniifolium Extracts
inferred← citeshttps://doi.org/10.1002/slct.202507164openalex-snapshot
Antioxidant and Enzyme Inhibitory Potential of Mespilus germanica L. Leaves: A Phytochemical and Molecular Docking Study
inferred← citeshttps://doi.org/10.1007/978-1-0716-0163-1_15openalex-snapshot
Ligand Fishing: An Approach for the Discovery of Inhibitors from Complex Biological Mixtures
inferred← citeshttps://doi.org/10.1007/978-1-4939-2447-9_11openalex-snapshot
Immobilized Magnetic Beads-Based Multi-Target Affinity Selection Coupled with HPLC-MS for Screening Active Compounds from Traditional Chinese Medicine and Natural Products
inferred← citeshttps://doi.org/10.1007/s00044-017-2014-7openalex-snapshot
α-Amylase and α-glucosidase inhibitory activities of the herbs of Artemisia dracunculus L. and its active constituents
inferred← citeshttps://doi.org/10.1007/s00044-024-03328-7openalex-snapshot
Design of novel benzimidazole-propane hydrazide derivatives as α-glucosidase and α-amylase inhibitors: in vitro and in silico studies
inferred← citeshttps://doi.org/10.1007/s00210-026-05249-1openalex-snapshot
Unnatural amino acid compounds as potent multi-target inhibitors of aldose reductase, α-glucosidase, and α-amylase: integrated in vitro, SAR, and molecular dynamics insights
inferred← citeshttps://doi.org/10.1007/s00217-025-04921-9openalex-snapshot
Exploring the multipharmacological potential of Rosa pisiformis: an integrated approach combining LC-MS/MS, GC-MS, enzyme inhibition, docking, and pathway enrichment
inferred← citeshttps://doi.org/10.1007/s00217-026-05265-8openalex-snapshot
In vitro and in silico investigation of Bingöl honey, the first and only Turkish polyfloral honey with European union geographical indication: comprehensive chemical characteristics and biological activities
inferred← citeshttps://doi.org/10.1007/s00253-019-10191-9openalex-snapshot
An overview of the biological production of 1-deoxynojirimycin: current status and future perspective
inferred← citeshttps://doi.org/10.1007/s10337-025-04414-7openalex-snapshot
Affinity Fishing of ACE Ligands from C. axillaris using Surface Functionalized Magnetic Nanoparticles
inferred← citeshttps://doi.org/10.1007/s10616-026-00955-3openalex-snapshot
Anticancer potential, antioxidant activity, chemical content, and enzyme inhibitory properties of Inula aschersoniana Janka, supported by an integrated network pharmacology study
inferred← citeshttps://doi.org/10.1007/s10616-026-01053-0openalex-snapshot
Integrated network pharmacology and in vitro/in silico evaluation of the bioactive potential of Gundelia komagenensis fırat extracts
inferred← citeshttps://doi.org/10.1007/s10811-013-0171-8openalex-snapshot
Macrocystis angustifolia is a potential source of enzyme inhibitors linked to type 2 diabetes and dementia
inferred← citeshttps://doi.org/10.1007/s11030-024-10911-yopenalex-snapshot
Investigation of cholinesterase and α-glucosidase enzyme activities, and molecular docking and dft studies for 1,2-disubstituted cyclopentane derivatives with phenyl and benzyl units
inferred← citeshttps://doi.org/10.1007/s11356-019-05915-3openalex-snapshot
The effects of naringin on different cyclophosphamide-induced organ toxicities in rats: investigation of changes in some metabolic enzyme activities
inferred← citeshttps://doi.org/10.1007/s11483-026-10129-5openalex-snapshot
Mechanistic Insights into the Biological Effects of Aronia melanocarpa Through In vitro Assays, Molecular Docking and Bioinformatic Analysis
inferred← citeshttps://doi.org/10.1007/s11694-019-00127-2openalex-snapshot
Sage (Salvia pilifera): determination of its polyphenol contents, anticholinergic, antidiabetic and antioxidant activities
inferred← citeshttps://doi.org/10.1007/s11694-021-00912-yopenalex-snapshot
Anticancer, anticholinesterase and antidiabetic activities of tunceli garlic (Allium tuncelianum): determining its phytochemical content by LC–MS/MS analysis
inferred← citeshttps://doi.org/10.1007/s11696-020-01375-zopenalex-snapshot
Biochemical constituent, enzyme inhibitory activity, and molecular docking analysis of an endemic plant species, Thymus migricus
inferred← citeshttps://doi.org/10.1007/s11696-026-04771-zopenalex-snapshot
Synthesis, enzyme inhibition, in silico molecular docking and DFT analysis of novel multi-functionalized thiourea and thiazolidinone benzenesulfonamides
inferred← citeshttps://doi.org/10.1007/s12010-019-03099-7openalex-snapshot
The Influence of Some Nonsteroidal Anti-inflammatory Drugs on Metabolic Enzymes of Aldose Reductase, Sorbitol Dehydrogenase, and α-Glycosidase: a Perspective for Metabolic Disorders
inferred← citeshttps://doi.org/10.1007/s12033-023-00766-3openalex-snapshot
Assessment of the Anti-Breast Cancer Effects of Urolithin with Molecular Docking Studies in the In Vitro Condition: Introducing a Novel Chemotherapeutic Drug
inferred← citeshttps://doi.org/10.1007/s13233-024-00247-9openalex-snapshot
Functionally substituted derivatives of novel thiourea and phenylthiourea as potent aldose reductase, α-amylase, and α-glycosidase inhibitors: in vitro and in silico studies
inferred← citeshttps://doi.org/10.1007/s13659-023-00424-wopenalex-snapshot
Flavonoids as dual-target inhibitors against α-glucosidase and α-amylase: a systematic review of in vitro studies
inferred← citeshttps://doi.org/10.1007/s13738-021-02331-8openalex-snapshot
Novel phenolic Mannich base derivatives: synthesis, bioactivity, molecular docking, and ADME-Tox Studies
inferred← citeshttps://doi.org/10.1007/s13738-025-03186-zopenalex-snapshot
Design, synthesis, and biological evaluation of 3-phenylimidazo[1,2-a]pyridine derivatives as diverse enzyme inhibitors
inferred← citeshttps://doi.org/10.1007/s13738-026-03367-4openalex-snapshot
Synthesis, single-crystal X-Ray, molecular docking studies, and metabolic enzyme inhibition properties of novel Co(II) metal complex
inferred← citeshttps://doi.org/10.1007/s44371-025-00301-0openalex-snapshot
Phytochemical profiling and pharmacological activities of ethanol and n-hexane extracts of Daniellia oliveri
inferred← citeshttps://doi.org/10.1007/s44371-026-00869-1openalex-snapshot
In vitro and in silico evaluation of antioxidant, anti-inflammatory, and antidiabetic activities of Allium schoenoprasum leaf extracts
inferred← citeshttps://doi.org/10.1016/b978-0-12-813280-7.00020-7openalex-snapshot
Enzyme and Bioactive Peptides—A Strategy for Discovery and Identification of Antihypertensive Peptides
inferred← citeshttps://doi.org/10.1016/b978-0-12-813822-9.00042-4openalex-snapshot
Traditional Herbal Products Used for the Management of Diabetes in Croatia: Linking Traditional Use With α-Glucosidase-Inhibitory Activity
inferred← citeshttps://doi.org/10.1016/b978-0-323-85748-2.00016-5openalex-snapshot
Role of magnetic polymer–coated nanoparticles in separation sciences
inferred← citeshttps://doi.org/10.1016/j.abb.2024.110099openalex-snapshot
Dynamics of small molecule-enzyme interactions: Novel benzenesulfonamides as multi-target agents endowed with inhibitory effects against some metabolic enzymes
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110368openalex-snapshot
Design, synthesis, and inhibition of α-glucosidase by novel l-phenylalanine-derived hydrazones: Kinetic, molecular docking, and dynamics studies
inferred← citeshttps://doi.org/10.1016/j.apjtm.2017.10.020openalex-snapshot
Phytochemical analysis and biological activities of Hertia cheirifolia L. roots extracts
inferred← citeshttps://doi.org/10.1016/j.apt.2020.05.020openalex-snapshot
Biogenic nano silver: Synthesis, characterization, antibacterial, antibiofilms, and enzymatic activity
inferred← citeshttps://doi.org/10.1016/j.arabjc.2021.103180openalex-snapshot
Photocatalytic degradation of Rhodamine B (RhB) dye in waste water and enzymatic inhibition study using cauliflower shaped ZnO nanoparticles synthesized by a novel One-pot green synthesis method
inferred← citeshttps://doi.org/10.1016/j.arabjc.2021.103193openalex-snapshot
Novel green synthesis, chemical characterization, toxicity, colorectal carcinoma, antioxidant, anti-diabetic, and anticholinergic properties of silver nanoparticles: A chemopharmacological study
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.103810openalex-snapshot
Assessment of antimicrobial and enzymes inhibition effects of Allium kastambulense with in silico studies: Analysis of its phenolic compounds and flavonoid contents
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.104626openalex-snapshot
Synthesis characterization and evaluation of novel triazole based analogs as a acetylcholinesterase and α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.152354openalex-snapshot
Novel heterocyclic organic compounds as DPP-4, α-amylase, and α-glucosidase inhibitors: Design, synthesis, and docking studies
inferred← citeshttps://doi.org/10.1016/j.bcab.2019.101441openalex-snapshot
Anticholinergic, antidiabetic and antioxidant activities of Anatolian pennyroyal (Mentha pulegium)-analysis of its polyphenol contents by LC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.bcab.2020.101711openalex-snapshot
Assessments of anticholinergic, antidiabetic, antioxidant activities and phenolic content of Stachys annua
inferred← citeshttps://doi.org/10.1016/j.bcab.2022.102417openalex-snapshot
Evaluation of the in vitro antioxidant, antidiabetic and anticholinergic properties of rosmarinic acid from rosemary (Rosmarinus officinalis L.)
inferred← citeshttps://doi.org/10.1016/j.bcab.2025.103646openalex-snapshot
Phytochemical analysis, molecular docking, in vitro cytotoxicity, enzyme inhibition and antioxidant activity of Viscum album subsp. austriacum in Turkey
inferred← citeshttps://doi.org/10.1016/j.bcp.2022.115376openalex-snapshot
Dipyridamole interacts with the N-terminal domain of HSP90 and antagonizes the function of the chaperone in multiple cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.08.003openalex-snapshot
Novel thymol bearing oxypropanolamine derivatives as potent some metabolic enzyme inhibitors – Their antidiabetic, anticholinergic and antibacterial potentials
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.10.012openalex-snapshot
Synthesis, characterization, crystal structure of the coordination polymer Zn(II) with thiosemicarbazone of glyoxalic acid and their inhibitory properties against some metabolic enzymes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.12.035openalex-snapshot
Synthesis and biological evaluation of novel tris-chalcones as potent carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.03.010openalex-snapshot
Synthesis and characterization of novel bromophenols: Determination of their anticholinergic, antidiabetic and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.102931openalex-snapshot
Novel eugenol bearing oxypropanolamines: Synthesis, characterization, antibacterial, antidiabetic, and anticholinergic potentials
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.102980openalex-snapshot
Synthesis of oxazolidinone from enantiomerically enriched allylic alcohols and determination of their molecular docking and biologic activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103134openalex-snapshot
Novel 2-aminopyridine liganded Pd(II) N-heterocyclic carbene complexes: Synthesis, characterization, crystal structure and bioactivity properties
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103298openalex-snapshot
Synthesis and investigation of polyhydroxylated pyrrolidine derivatives as novel chemotypes showing dual activity as glucosidase and aldose reductase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103313openalex-snapshot
Novel tribenzylaminobenzolsulphonylimine based on their pyrazine and pyridazines: Synthesis, characterization, antidiabetic, anticancer, anticholinergic, and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103333openalex-snapshot
ICP-MS and HPLC analyses, enzyme inhibition and antioxidant potential of Achillea schischkinii Sosn.
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103647openalex-snapshot
Cholinesterases, α-glycosidase, and carbonic anhydrase inhibition properties of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives: Synthetic analogues for the treatment of Alzheimer's disease and diabetes mellitus
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103762openalex-snapshot
Novel functionally substituted esters based on sodium diethyldithiocarbamate derivatives: Synthesis, characterization, biological activity and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103924openalex-snapshot
Synthesis, bioactivity and binding energy calculations of novel 3-ethoxysalicylaldehyde based thiosemicarbazone derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103969openalex-snapshot
Novel propanolamine derivatives attached to 2-metoxifenol moiety: Synthesis, characterization, biological properties, and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104002openalex-snapshot
Synthesis, α-glucosidase inhibition and in silico studies of some 4-(5-fluoro-2-substituted-1H-benzimidazol-6-yl)morpholine derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104171openalex-snapshot
Synthesis of nitrogen, phosphorus, selenium and sulfur-containing heterocyclic compounds – Determination of their carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase and α-glycosidase inhibition properties
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104216openalex-snapshot
Novel cyclic thiourea derivatives of aminoalcohols at the presence of AlCl3 catalyst as potent α-glycosidase and α-amylase inhibitors: Synthesis, characterization, bioactivity investigation and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104554openalex-snapshot
Probing 4-(diethylamino)-salicylaldehyde-based thiosemicarbazones as multi-target directed ligands against cholinesterases, carbonic anhydrases and α-glycosidase enzymes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105032openalex-snapshot
Fatty acid composition, enzyme inhibitory effect, antioxidant and anticancer activity of extract from Saponaria prostrata WILLD. subsp. anatolica HEDGE
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105069openalex-snapshot
Synthesis, biological activity and docking calculations of bis-naphthoquinone derivatives from Lawsone
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105566openalex-snapshot
Selenourea and thiourea derivatives of chiral and achiral enetetramines: Synthesis, characterization and enzyme inhibitory properties
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106115openalex-snapshot
Synthetic access to syn-functionalised chiral hydroxy pyrrolidines and pyrrolidones: Evaluation of α-glucosidase inhibition activity, docking studies and pharmacokinetics prediction
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106846openalex-snapshot
Discovery of novel 4,5-diphenyl-imidazol-α-aminophosphonate hybrids as promising anti-diabetic agents: Design, synthesis, in vitro, and in silico enzymatic studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107207openalex-snapshot
Pyrano[2,3-b]chromone derivatives as novel dual inhibitors of α-glucosidase and α-amylase: Design, synthesis, biological evaluation, and in silico studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109086openalex-snapshot
Effects of some 7-hydroxy coumarin compounds on coagulation factor Xa, urease and antidiabetic enzymes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110061openalex-snapshot
Novel pyridazinone-based N-phenylacetamides as α-glucosidase-selective and dual α-glucosidase/aldose reductase inhibitors: Synthesis, SAR analysis, and cytotoxicity evaluation
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.07.093openalex-snapshot
Hepatoprotective effect of Opuntia microdasys (Lehm.) Pfeiff flowers against diabetes type II induced in rats
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118264openalex-snapshot
Development of phenolic Mannich bases as α-glucosidase and aldose reductase inhibitors: In vitro and in silico approaches for managing diabetes mellitus and its complications
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128722openalex-snapshot
Polyphenolic compounds: Synthesis, assessment of antimicrobial effect and enzymes inhibition against important medicinal enzymes with computational details
inferred← citeshttps://doi.org/10.1016/j.bmcl.2025.130498openalex-snapshot
Synthesis of new Pyridazinone derivatives and their dual inhibitory activity on aldose reductase and α-glucosidase
inferred← citeshttps://doi.org/10.1016/j.bmcl.2026.130710openalex-snapshot
Novel 1H-pyrrole-2,5-dione derivatives as potential anti-diabetic agents: design, synthesis, in vitro, in ovo, and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bpc.2021.106629openalex-snapshot
Enzyme inhibitory function and phytochemical profile of Inula discoidea using in vitro and in silico methods
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110655openalex-snapshot
Novel coumarin-chalcone derivatives: Synthesis, characterization, antioxidant, cyclic voltammetry, molecular modelling and biological evaluation studies as acetylcholinesterase, α-glycosidase, and carbonic anhydrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.chmed.2020.03.003openalex-snapshot
Chemical constituents from acid hydrolyzates of Panax quinquefolius total saponins and their inhibition activity to α-glycosidase and protein tyrosine phosphatase 1B
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.03.002openalex-snapshot
Fabrication of enzyme-immobilized halloysite nanotubes for affinity enrichment of lipase inhibitors from complex mixtures
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.09.006openalex-snapshot
Advanced development in phytochemicals analysis of medicine and food dual purposes plants used in China (2011–2014)
inferred← citeshttps://doi.org/10.1016/j.chroma.2016.09.022openalex-snapshot
Screening of thrombin inhibitors from phenolic acids using enzyme-immobilized magnetic beads through direct covalent binding by ultrahigh-performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.chroma.2025.466469openalex-snapshot
Separation and enrichment of active components in Toddalia asiatica (L.) Lam.by carboxylated chitosan-modified magnetic metal-organic frameworks
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2021.127839openalex-snapshot
Effects of some phenolic compounds on the inhibition of α-glycosidase enzyme-immobilized on Pluronic®F127 micelles: An in vitro and in silico study
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2020.111400openalex-snapshot
A colorimetric method for screening α-glucosidase inhibitors from flavonoids using 3,3′,5,5′-tetramethylbenzidine as a chromogenic probe
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2022.100082openalex-snapshot
Nimesulide linked acyl thioureas potent carbonic anhydrase I, II and α-glucosidase inhibitors: Design, synthesis and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2022.110032openalex-snapshot
Production of α-glucosidase inhibitor in the intestines by Bacillus licheniformis
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.104209openalex-snapshot
In vitro and in silico based assessment of biological activity of endemic Allium species: LC-MS/MS analysis of onions
inferred← citeshttps://doi.org/10.1016/j.fbio.2025.106835openalex-snapshot
Comprehensive UPLC-MS/MS-based metabolic profiling, antioxidant potential, enzyme inhibition, and molecular docking studies of Ficus carica L. leaves: Potential for functional food applications
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.109368openalex-snapshot
Synthesis and biological evaluation of novel sesamol analogs targeting acetylcholinesterase, α-glycosidase, and carbonic anhydrase enzymes
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105343openalex-snapshot
Anti-hyperlipidemia on rats in vivo and new compounds from the seeds of Psoralea corylifolia
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106213openalex-snapshot
Untargeted metabolomics profiling of Morus alba twigs extract and antibacterial activity of pure metabolites
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