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Acta Pharmaceutica Sinica ; (12): 716-724, 2012.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-276254

RESUMO

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.


Assuntos
Animais , Humanos , Compostos Benzidrílicos , Química , Farmacologia , Diabetes Mellitus Tipo 2 , Tratamento Farmacológico , Glucosídeos , Química , Farmacologia , Hipoglicemiantes , Química , Farmacologia , Estrutura Molecular , Monossacarídeos , Química , Farmacologia , Transportador 1 de Glucose-Sódio , Metabolismo , Transportador 2 de Glucose-Sódio , Metabolismo , Relação Estrutura-Atividade
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