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
From carbohydrates to drug-like fragments: Rational development of novel α-amylase inhibitors - ScienceDirect
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
Interaction of Structurally Diverse Phenolic Compounds with Porcine Pancreatic α-Amylase | Journal of Agricultural and Food Chemistry
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
Interaction of Structurally Diverse Phenolic Compounds with Porcine Pancreatic α-Amylase | Journal of Agricultural and Food Chemistry
Molecules | Free Full-Text | Evaluation of the Anti-Cancer Potential of Rosa damascena Mill. Callus Extracts against the Human Colorectal Adenocarcinoma Cell Line
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
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal 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
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
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal Chemistry
Identification of Human Toll-like Receptor 2-Agonistic Activity in Dihydropyridine–Quinolone Carboxamides | ACS Medicinal Chemistry Letters
Order and Disorder: Differential Structural Impacts of Myricetin and Ethyl Caffeate on Human Amylase, an Antidiabetic Target | Journal of Medicinal Chemistry
Virtual Screening Against Carbohydrate-Binding Proteins: Evaluation and Application to Bacterial Burkholderia ambifaria Lectin | Journal of Chemical Information and Modeling
PDF) Anthocyanin composition, antioxidant efficiency, and -amylase inhibitor activity of different Hungarian sour cherry varieties (Prunus cerasus L.)
Molecules | Free Full-Text | Truly Target-Focused Pharmacophore Modeling: A Novel Tool for Mapping Intermolecular Surfaces
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
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Isolation of a New Phlorotannin, a Potent Inhibitor of Carbohydrate-Hydrolyzing Enzymes, from the Brown Alga Sargassum patens | 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
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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
How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information | Journal of Chemical Information and Modeling
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
How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information | Journal of Chemical Information and Modeling
PDF) Truly Target-Focused Pharmacophore Modeling: A Novel Tool for Mapping Intermolecular Surfaces
MDPI Docking | PDF | Drug Design | Docking (Molecular)
PDF) Arginase Structure and Inhibition: Catalytic Site Plasticity Reveals New Modulation Possibilities
