PMID

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

Kindai University

Synthesis of novel inhibitors ofa-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies.

Universiti Teknologi Mara (Uitm)

Identification and development of biphenyl substituted iminosugars as improved dual glucosylceramide synthase/neutral glucosylceramidase inhibitors.

Leiden University

Probing the active-site requirements of human intestinal N-terminal maltase-glucoamylase: Synthesis and enzyme inhibitory activities of a six-membered ring nitrogen analogue of kotalanol and its de-O-sulfonated derivative.

Simon Fraser University

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

Toyama Medical and Pharmaceutical University

Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.

Hokuriku University

Synthesis and alpha-D-glucosidase inhibitory activity of N-substituted valiolamine derivatives as potential oral antidiabetic agents.

TBA

 

Synthesis of potent -D-glucocerebrosidase inhibitors: N-alkyl--valienamines

TBA

Selectivity of 3'-O-methylponkoranol for inhibition of N- and C-terminal maltase glucoamylase and sucrase isomaltase, potential therapeutics for digestive disorders or their sequelae.

Simon Fraser University

Probing the active-site requirements of human intestinal N-terminal maltase glucoamylase: the effect of replacing the sulfate moiety by a methyl ether in ponkoranol, a naturally occurringa-glucosidase inhibitor.

Simon Fraser University

Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor.

Simon Fraser University

Dual-action lipophilic iminosugar improves glycemic control in obese rodents by reduction of visceral glycosphingolipids and buffering of carbohydrate assimilation.

Leiden University

 

New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases

TBA

Synthesis of andrographolide derivatives: a new family of alpha-glucosidase inhibitors.

Zhengzhou University

Studies on the novel alpha-glucosidase inhibitory activity and structure-activity relationships for andrographolide analogues.

Zhengzhou University

Synergetic inhibition of genistein and D-glucose on alpha-glucosidase.

Sun Yat-Sen (Zhongshan) University

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

Hokuriku University

Bioactive Asarone-Derived Phenylpropanoids from the Rhizome of Acorus tatarinowii Schott.

College of Pharmacy/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of Tcm and New Drugs Research