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26 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
26343830 15 New arylalkanones from Horsfieldia macrobotrys, effective antidiabetic agents concomitantly inhibitinga-glucosidase and free radicals.EBI Chulalongkorn University
26287401 39 Lanostane Triterpenes from the Tibetan Medicinal Mushroom Ganoderma leucocontextum and Their Inhibitory Effects on HMG-CoA Reductase anda-Glucosidase.EBI Chinese Academy of Sciences
24973028 29 Synthesis and biological evaluation ofa-1-C-4'-arylbutyl-L-arabinoiminofuranoses, a new class ofa-glucosidase inhibitors.EBI Tohoku Pharmaceutical University
23811091 20 Quercitylcinnamates, a new series of antidiabetic bioconjugates possessinga-glucosidase inhibition and antioxidant.EBI Chulalongkorn University
23810673 107 Synthesis anda-glucosidase inhibitory activity evaluation of N-substituted aminomethyl--d-glucopyranosides.EBI Xi'an Jiaotong University
23466232 48 A new series of N2-substituted-5-(p-toluenesulfonylamino)phthalimide analogues asa-glucosidase inhibitors.EBI Xi'an Jiaotong University
23106358 96 a-1-C-butyl-1,4-dideoxy-1,4-imino-l-arabinitol as a second-generation iminosugar-based orala-glucosidase inhibitor for improving postprandial hyperglycemia.EBI University of Toyama
23031648 30 Role of the side chain stereochemistry in thea-glucosidase inhibitory activity of kotalanol, a potent naturala-glucosidase inhibitor. Part 2.EBI Kinki University
22818971 3 (+)-Pinoresinol is a putative hypoglycemic agent in defatted sesame (Sesamum indicum) seeds though inhibitinga-glucosidase.EBI Chulalongkorn University
21345683 42 Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potenta-glucosidase inhibitors.EBI Kinki University
18547114 18 Alpha-glucosidase inhibitor from Kothala-himbutu (Salacia reticulata WIGHT).EBI Fuji-Sangyo Co., Ltd.
18595718 51 In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures.EBI Hokuriku University
9651160 52 Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.EBI Hokuriku University
7966130 69 Nitrogen-in-the-ring pyranoses and furanoses: structural basis of inhibition of mammalian glycosidases.EBI Hokuriku University
22290077 3 Concise synthesis of (+)-conduritol F and inositol analogues from naturally available (+)-proto-quercitol and their glucosidase inhibitory activity.EBI Chulalongkorn University
22209731 81 Antidiabetogenic oligostilbenoids and 3-ethyl-4-phenyl-3,4-dihydroisocoumarins from the bark of Shorea roxburghii.EBI Kinki University
21454075 24 Biological evaluation of 3'-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3' position in the side chain on thea-glucosidase inhibitory activity.EBI Kinki University
21420866 29 Role of the side chain stereochemistry in thea-glucosidase inhibitory activity of kotalanol, a potent naturala-glucosidase inhibitor.EBI Kinki University
21397496 4 Selectivea-glucosidase substrates and inhibitors containing short aromatic peptidyl moieties.EBI Seoul National University
21185187 42 The synthesis and biological evaluation of 1-C-alkyl-L-arabinoiminofuranoses, a novel class ofa-glucosidase inhibitors.EBI Tohoku Pharmaceutical University
19835391 4 Total synthesis of (-)-uniflorine A.EBI Universit£ di Firenze
19362832 4 Synthetic studies in butenonyl C-glycosides: Preparation of polyfunctional alkanonyl glycosides and their enzyme inhibitory activity.EBI Central Drug Research Institute
15165148 13 Glycosidase-inhibiting pyrrolidines and pyrrolizidines with a long side chain in Scilla peruviana.EBI Hokuriku University
12502331 28 New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibirica.EBI Hokuriku University
11858756 25 New sugar-mimic alkaloids from the pods of Angylocalyx pynaertii.EBI Hokuriku University
9599261 12 Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis.EBI Hokuriku University