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Research progress of sodium-glucose co-transporter 2 inhibitors for treatment of type 2 diabetes / 药学学报
Acta Pharmaceutica Sinica ; (12): 716-724, 2012.
Article in Chinese | WPRIM | ID: wpr-276254
ABSTRACT
Sodium-glucose co-transporters are a family of glucose transporter found in the intestinal mucosa of the small intestine (SGLT-2) and the proximal tubule of the nephron (SGLT-1 and SGLT-2). They contribute to renal glucose reabsorption and most of renal glucose (about 90%) is reabsorbed by SGLT-2 located in the proximal renal tubule. Selectively inhibiting activity of SGLT-2 is an innovative therapeutic strategy for treatment of type 2 diabetes by enhancing urinary glucose excretion from the body. Therefore SGLT-2 inhibitors are considered to be potential antidiabetic drugs with an unique mechanism. This review will highlight some recent advances and structure-activity relationships in the discovery and development of SGLT-2 inhibitors including O-glycoside, C-glycoside, C, O-spiro glycoside and non glycosides.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Structure-Activity Relationship / Benzhydryl Compounds / Molecular Structure / Chemistry / Diabetes Mellitus, Type 2 / Drug Therapy / Sodium-Glucose Transporter 1 / Sodium-Glucose Transporter 2 / Glucosides Limits: Animals / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Structure-Activity Relationship / Benzhydryl Compounds / Molecular Structure / Chemistry / Diabetes Mellitus, Type 2 / Drug Therapy / Sodium-Glucose Transporter 1 / Sodium-Glucose Transporter 2 / Glucosides Limits: Animals / Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article