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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis and biological evaluation of an orally active ghrelin agonist that stimulates food consumption and adiposity in rats.
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Synthesis and biological evaluation of an orally active ghrelin agonist that stimulates food consumption and adiposity in rats.

机译:口服活性促生长素释放肽激动剂的合成和生物学评估,该激动剂刺激大鼠进食和肥胖。

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摘要

2-(2-Amino-2-methyl-propionylamino)-5-phenyl-pentanoic acid {1-[1-(4-methoxy-phenyl)-1-methyl-2-oxo-2-pyrrolidin-1-yl-ethyl]-1H-imidaz ol-4-yl}-amide (LY444711, 6) is an orally active ghrelin agonist that binds with high affinity to and is a potent activator of the growth hormone secretagogue receptor 1a (GHS-R1a) receptor. In rat models of feeding behavior and pharmacology, 6 creates a positive energy balance and induces adiposity by stimulating food consumption and sparing fat utilization. As an orally active ghrelin agonist, 6 represents a new pharmacological tool to investigate the orexigenic role of ghrelin in regulating energy homeostasis.
机译:2-(2-氨基-2-甲基-丙酰基氨基)-5-苯基戊酸{1- [1-(4-甲氧基-苯基)-1-甲基-2-氧-2-吡咯烷-1-基-乙基] -1H-咪唑醇-4-基}-酰胺(LY444711,6)是一种口服活性促生长素释放肽激动剂,与生长激素促分泌素受体1a(GHS-R1a)受体具有很高的亲和力,是一种有效的激活剂。在大鼠的进食行为和药理模型中,6建立正能量平衡并通过刺激食物消耗和节省脂肪利用来诱发肥胖。作为一种口服活性ghrelin激动剂,6代表一种新的药理学工具,用于研究ghrelin在调节能量稳态中的致癌作用。

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