Topological, hydrophobicity, and other descriptors on α-glucosidase inhibition: a QSAR study on xanthone derivatives
Author:
Affiliation:
1. REQUIMTE, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 687 Rua do Campo Alegre, Porto, Portugal
Publisher
Informa UK Limited
Subject
Drug Discovery,Pharmacology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.3109/14756366.2010.549089
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1. Computer-aided Molecular Design of Novel Glucosidase Inhibitors for AIDS Treatment
2. The alpha-glucosidase inhibitor N-butyldeoxynojirimycin inhibits human immunodeficiency virus entry at the level of post-CD4 binding
3. Inhibition of alpha-glucosidase I of the glycoprotein-processing enzymes by 6-O-butanoyl castanospermine (MDL 28,574) and its consequences in human immunodeficiency virus-infected T cells
4. Toward the Virtual Screening of α-Glucosidase Inhibitors with the Homology-Modeled Protein Structure
5. Synthesis and evaluation of the α-glucosidase inhibitory activity of 3-[4-(phenylsulfonamido)benzoyl]-2H-1-benzopyran-2-one derivatives
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