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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Novel glitazones: design, synthesis, glucose uptake and structure-activity relationships.
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Novel glitazones: design, synthesis, glucose uptake and structure-activity relationships.

机译:新型格列酮:设计,合成,葡萄糖吸收和构效关系。

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摘要

Glitazones are known to exhibit antihyperglycemic activity by decreasing peripheral insulin resistance. In the present study, we have designed some novel glitazones based on the structure-activity relationships as possible PPAR-gamma agonists. The manually designed glitazones were synthesized by using the appropriate synthetic schemes and screened for their in vitro antihyperglycemic activity by estimating glucose uptake by rat hemi-diaphragm, both in the absence and in the presence of external insulin. Some of the glitazones exhibited good antihyperglycemic activity in presence of insulin. Illustration about their design, synthesis, evaluation, and structure-activity relationships is described.
机译:已知格列唑酮通过降低外周胰岛素抵抗表现出降血糖活性。在本研究中,我们基于结构-活性关系设计了一些新颖的格列酮,作为可能的PPAR-γ激动剂。通过使用适当的合成方案合成了人工设计的格列酮,并在不存在和存在外部胰岛素的情况下,通过估计大鼠半膜片摄取的葡萄糖来筛选它们的体外降血糖活性。某些格列酮在胰岛素存在下表现出良好的降血糖活性。描述了有关它们的设计,合成,评估和构效关系的图示。

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