摘要
在药物化学中很少有一个配体可以用来研究在药理学过程中的两个独立现象。镇痛药和其他同型二聚体配体的发现给科学家们提供了一个工具,不仅探究了如何提高配体的功效,也探究了受体的异源和同源二聚体之间可能的相互作用。作为一个直型配体,镇痛药可以让科学家通过直接修改其残基从而影响其与受体message-address相互作用进而增加疗效。为了提高疗效,这就引领了对配体linker的探索,正是对连接物的修改,从而发现受体系统二聚化的发生是对信号转导的二次调制。最近,通过bitopicity的发现,linker的优点似乎是调节相应受体进而增加配体的结合和信号转导。这是在结合linker末端处的配体之前,通过可能的轻微的受体构象变化而完成的。这些进展是由已故的Andrzej W. Lipkowski教授所做的工作。本文为镇痛药奠基,同时祝贺Lipkowski教授在这个领域所作出的贡献。
关键词: Biphalin
Current Medicinal Chemistry
Title:Biphalin: The Foundation of Bivalent Ligands
Volume: 23 Issue: 29
Author(s): Scott M. Cowell, Yeon Sun Lee
Affiliation:
关键词: Biphalin
摘要: Seldom in medicinal chemistry does one ligand present the ability to study two separate phenomena in a pharmacological process. The discovery of biphalin with other homodimeric ligands has given scientists a tool that not only explores how to increase the efficacy of the ligand, but also explore the possible interactions of hetero and homo dimerization of the receptors themselves. As a straight ligand, biphalin has allowed scientists to increase efficacy by direct modification of the residues to affect the message-address interactions with receptors. This led to the exploration of ligand linkers to increase efficacy and it was this modification of the linkers led to discoveries that suggested dimerization of receptor system occurs as a secondary modulation of signal transduction. Even more recently, exploration of the advances in linkers through the discovery of bitopicity seems to modulate the actual receptors to increase the binding and signal transdcution of the ligand. This is accomplished by possible slight conformational changes in the receptors before binding of the ligand located at the end of the linker. These advances were made by the work of the late Prof. Andrzej W. Lipkowski. This review gives the foundation of biphalin and in turn celebrates the contributions of Prof. Lipkowski made in this area.
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Cite this article as:
Scott M. Cowell, Yeon Sun Lee , Biphalin: The Foundation of Bivalent Ligands, Current Medicinal Chemistry 2016; 23 (29) . https://dx.doi.org/10.2174/0929867323666160510122731
DOI https://dx.doi.org/10.2174/0929867323666160510122731 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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