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Synthesis of phenyloxyisobutyric acid derivatives and their antidiabetic activity in vitro / 药学学报
Acta Pharmaceutica Sinica ; (12): 108-114, 2006.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-408803
Responsible library: WPRO
ABSTRACT
Aim To design and synthesize new phenyloxyisobutyric acid analogues as antidiabetic compounds. Methods Eight new target compounds were synthesized by combination of lipophilic moieties and acidic moiety with nucleophilic replacement or Mitsunobu condensation. The eight compounds were confirmed by 1H NMR, 13C NMR, IR and MS. Results In vitro insulin-sensitizing activity (3T3-L1adipocyte) demonstrated, that the cultured glucose concentration of up-clear solution detected with GODpioglitazone, compounds A and B were added to the insulin-resistant system. Conclusion In vitro insulin-sensitizing activity of target compound A is in between that of rosiglitazone and pioglitazone, and activity of target compound B is slightly less than that of pioglitazone.

Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2006 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2006 Document type: Article
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