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Identification of novel indole derivatives as highly potent AMPK activators with anti-diabetic profiles.
Tamura, Yuusuke; Morita, Ippei; Hinata, Yu; Kojima, Eiichi; Ozasa, Hiroki; Ikemoto, Hidaka; Asano, Mutsumi; Wada, Toshihiro; Hayasaki-Kajiwara, Yoko; Iwasaki, Takanori; Matsumura, Kenichi.
Afiliação
  • Tamura Y; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan. Electronic address: yuusuke.tamura@shionogi.co.jp.
  • Morita I; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Hinata Y; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Kojima E; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Ozasa H; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Ikemoto H; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Asano M; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Wada T; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Hayasaki-Kajiwara Y; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Iwasaki T; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
  • Matsumura K; Shionogi Pharmaceutical Research Center, Shionogi & Co., Ltd., 1-1, Futabacho 3-chome, Toyonaka, Osaka 561-0825, Japan.
Bioorg Med Chem Lett ; 68: 128769, 2022 07 15.
Article em En | MEDLINE | ID: mdl-35513222
ABSTRACT
AMP-activated protein kinase (AMPK) has been shown to play an important role in the beneficial effects of exercise on glucose and lipid metabolism in skeletal muscle and liver. Therefore, activation of AMPK has been proposed as an attractive strategy for the treatment of metabolic disorders, such as type 2 diabetes. Many of existing AMPK activators bearing diverse chemical structure were reported. However, there have been few reports of direct AMPK activator with high potency for ß2-AMPK isoform, which is thought to be important for glucose homeostasis, and their chemical structure is limited to benzimidazole core. We describe herein our efforts for identification of novel AMPK activator. Our newly designed 4-azaindole derivative 16g exhibited single-digit nM in vitro activity, and chronic treatment with 16g led to dose-dependent improvement in HbA1c as well as decrease in hepatic lipid accumulation in diabetic animal model.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Proteínas Quinases Ativadas por AMP Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Proteínas Quinases Ativadas por AMP Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2022 Tipo de documento: Article