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A novel class ofa-glucosidase and HMG-CoA reductase inhibitors from Ganoderma leucocontextum and the anti-diabetic properties of ganomycin I in KK-A

Chinese Academy Of Sciences

Synthesis and characterization of novel, conjugated, fluorescent DNJ derivatives fora-glucosidase recognition.

Shibaura Institute Of Technology

Hydrophobic substituents increase the potency of salacinol, a potenta-glucosidase inhibitor from Ayurvedic traditional medicine 'Salacia'.

Kindai University

Design, synthesis and biological evaluation of 3'-benzylated analogs of 3'-epi-neoponkoranol as potenta-glucosidase inhibitors.

China Pharmaceutical University

New arylalkanones from Horsfieldia macrobotrys, effective antidiabetic agents concomitantly inhibitinga-glucosidase and free radicals.

Chulalongkorn University

Lanostane Triterpenes from the Tibetan Medicinal Mushroom Ganoderma leucocontextum and Their Inhibitory Effects on HMG-CoA Reductase anda-Glucosidase.

Chinese Academy Of Sciences

Synthesis and biological evaluation ofa-1-C-4'-arylbutyl-L-arabinoiminofuranoses, a new class ofa-glucosidase inhibitors.

Tohoku Pharmaceutical University

Amine-linked diquercitols as newa-glucosidase inhibitors.

Chulalongkorn University

Rat intestinal sucrase inhibition of constituents from the roots of Rosa rugosa Thunb.

Chungnam National University

Quercitylcinnamates, a new series of antidiabetic bioconjugates possessinga-glucosidase inhibition and antioxidant.

Chulalongkorn University

Synthesis anda-glucosidase inhibitory activity evaluation of N-substituted aminomethyl-ß-d-glucopyranosides.

Xi'An Jiaotong University

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.

University Of Toyama

Role of the side chain stereochemistry in thea-glucosidase inhibitory activity of kotalanol, a potent naturala-glucosidase inhibitor. Part 2.

Kinki University

Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potenta-glucosidase inhibitors.

Kinki University

Alpha-glucosidase inhibitor from Kothala-himbutu (Salacia reticulata WIGHT).

Fuji-Sangyo

In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures.

Hokuriku University

Iminosugar-producing Thai medicinal plants.

Hokuriku University

Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases.

Hokuriku University

2-Aminoresorcinol is a potent alpha-glucosidase inhibitor.

Hokkaido University

Biological properties of D- and L-1-deoxyazasugars.

Toyama Medical And Pharmaceutical University

Alpha-1-C-alkyl-1-deoxynojirimycin derivatives as potent and selective inhibitors of intestinal isomaltase: remarkable effect of the alkyl chain length on glycosidase inhibitory profile.

Universit£

Concise synthesis of (+)-conduritol F and inositol analogues from naturally available (+)-proto-quercitol and their glucosidase inhibitory activity.

Chulalongkorn University

Antidiabetogenic oligostilbenoids and 3-ethyl-4-phenyl-3,4-dihydroisocoumarins from the bark of Shorea roxburghii.

Kinki University

Docking and SAR studies of D- and L-isofagomine isomers as humanß-glucocerebrosidase inhibitors.

University Of Toyama

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.

Kinki University

Role of the side chain stereochemistry in thea-glucosidase inhibitory activity of kotalanol, a potent naturala-glucosidase inhibitor.

Kinki University

The synthesis and biological evaluation of 1-C-alkyl-L-arabinoiminofuranoses, a novel class ofa-glucosidase inhibitors.

Tohoku Pharmaceutical University

Total synthesis of (-)-uniflorine A.

Universit£

Fagomine isomers and glycosides from Xanthocercis zambesiaca.

Hokuriku University

 

New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases

TBA

New sugar-mimic alkaloids from the pods of Angylocalyx pynaertii.

Hokuriku University

Cernuosides A and B, two sucrase inhibitors from Pulsatilla cernua.

China Pharmaceutical University

Baicalein, an alpha-glucosidase inhibitor from Scutellaria baicalensis.

Hokkaido University

Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis.

Hokuriku University

N-alkylated nitrogen-in-the-ring sugars: conformational basis of inhibition of glycosidases and HIV-1 replication.

Hokuriku University