Szövés Becslés Felismer mortier gyémánt med chem lett 2016 belső Ki Fúró
Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition - ScienceDirect
MDPI Docking | PDF | Drug Design | Docking (Molecular)
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal Chemistry
PDF) Anthocyanin composition, antioxidant efficiency, and -amylase inhibitor activity of different Hungarian sour cherry varieties (Prunus cerasus L.)
Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition - ScienceDirect
Identification of Human Toll-like Receptor 2-Agonistic Activity in Dihydropyridine–Quinolone Carboxamides | ACS Medicinal Chemistry Letters
PDF) Alpha-Amylase Modulation: Discovery of Inhibitors Using a Multi-Pharmacophore Approach for Virtual Screening | Jérémie Mortier - Academia.edu
Dietary Antioxidant Anthocyanins Mitigate Type II Diabetes through Improving the Disorder of Glycometabolism and Insulin Resistance | Journal of Agricultural and Food Chemistry
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How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information | Journal of Chemical Information and Modeling
Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition - ScienceDirect
Molecules | Free Full-Text | Truly Target-Focused Pharmacophore Modeling: A Novel Tool for Mapping Intermolecular Surfaces
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal Chemistry
PDF) Extending the investigation of 4-thiazolidinone derivatives as potential multi-target ligands of enzymes involved in diabetes mellitus and its long-term complications: A study with pancreatic α-amylase
Interaction of Structurally Diverse Phenolic Compounds with Porcine Pancreatic α-Amylase | Journal of Agricultural and Food Chemistry
IJMS | Free Full-Text | Comparison of the Modulating Effect of Anthocyanin-Rich Sour Cherry Extract on Occludin and ZO-1 on Caco-2 and HUVEC Cultures
Molecules | Free Full-Text | Evaluation of the Anti-Cancer Potential of Rosa damascena Mill. Callus Extracts against the Human Colorectal Adenocarcinoma Cell Line
IJMS | Free Full-Text | Comparison of the Modulating Effect of Anthocyanin-Rich Sour Cherry Extract on Occludin and ZO-1 on Caco-2 and HUVEC Cultures
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Pharmaceutics | Free Full-Text | Effects of Polyphenols on P-Glycoprotein (ABCB1) Activity
PDF) Inhibition studies on α-amylase using isothermal titration calorimetry
Virtual Screening Against Carbohydrate-Binding Proteins: Evaluation and Application to Bacterial Burkholderia ambifaria Lectin | Journal of Chemical Information and Modeling
From carbohydrates to drug-like fragments: Rational development of novel α-amylase inhibitors - ScienceDirect
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal Chemistry
Interaction of Structurally Diverse Phenolic Compounds with Porcine Pancreatic α-Amylase | Journal of Agricultural and Food Chemistry
How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information | Journal of Chemical Information and Modeling
Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition - ScienceDirect
PDF) Arginase Structure and Inhibition: Catalytic Site Plasticity Reveals New Modulation Possibilities
How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information | Journal of Chemical Information and Modeling
From Carbohydrates to Drug-Like Fragments: Rational Development of Novel α-Amylase Inhibitors