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促甲状腺激素释放激素类似物

Thyrotropin-releasing hormone analogs.

作者信息

Colson A O, Gershengorn M C

机构信息

Clinical Endocrinology Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 50 South Drive, Bldg 50/4134, Bethesda, MD 20892, USA.

出版信息

Mini Rev Med Chem. 2006 Feb;6(2):221-6. doi: 10.2174/138955706775476019.

Abstract

Thyrotropin releasing hormone (TRH: pyroglutamic acid-histidine-prolineamide) regulates the activity of cells in the anterior pituitary and within the central and peripheral nervous systems. TRH, which has been the subject of much research over the past three decades, exerts its effects by acting through class A G-protein coupled receptors. The recent discovery of a second receptor subtype has generated an interest in the discovery of receptor subtype-selective TRH analogs. In this review, we describe advances in the development of TRH analogs and in the understanding of their mechanism of interaction with TRH receptors. We also describe the recent breakthrough in the identification of analogs that bind selectively at TRH-R2.

摘要

促甲状腺激素释放激素(TRH:焦谷氨酸-组氨酸-脯氨酰胺)调节腺垂体以及中枢和外周神经系统中细胞的活性。在过去三十年里,TRH一直是大量研究的主题,它通过作用于A类G蛋白偶联受体发挥作用。最近发现的第二种受体亚型引发了人们对发现受体亚型选择性TRH类似物的兴趣。在这篇综述中,我们描述了TRH类似物开发方面的进展以及对其与TRH受体相互作用机制的理解。我们还描述了在鉴定选择性结合TRH-R2的类似物方面的最新突破。

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