Suppr超能文献

氟在药物化学中的应用。

Applications of Fluorine in Medicinal Chemistry.

作者信息

Gillis Eric P, Eastman Kyle J, Hill Matthew D, Donnelly David J, Meanwell Nicholas A

机构信息

Department of Discovery Chemistry, Bristol-Myers Squibb Research and Development , 5 Research Parkway, Wallingford, Connecticut 06492, United States.

Discovery Chemistry Platforms, PET Radiochemical Synthesis, Bristol-Myers Squibb Research and Development , P.O. Box 4000, Princeton, New Jersey 08543, United States.

出版信息

J Med Chem. 2015 Nov 12;58(21):8315-59. doi: 10.1021/acs.jmedchem.5b00258. Epub 2015 Jul 22.

Abstract

The role of fluorine in drug design and development is expanding rapidly as we learn more about the unique properties associated with this unusual element and how to deploy it with greater sophistication. The judicious introduction of fluorine into a molecule can productively influence conformation, pKa, intrinsic potency, membrane permeability, metabolic pathways, and pharmacokinetic properties. In addition, (18)F has been established as a useful positron emitting isotope for use with in vivo imaging technology that potentially has extensive application in drug discovery and development, often limited only by convenient synthetic accessibility to labeled compounds. The wide ranging applications of fluorine in drug design are providing a strong stimulus for the development of new synthetic methodologies that allow more facile access to a wide range of fluorinated compounds. In this review, we provide an update on the effects of the strategic incorporation of fluorine in drug molecules and applications in positron emission tomography.

摘要

随着我们对这种独特元素相关的独特性质以及如何更巧妙地运用它有了更多了解,氟在药物设计与开发中的作用正在迅速扩展。将氟明智地引入分子中可以有效地影响构象、pKa值、内在活性、膜通透性、代谢途径以及药代动力学性质。此外,氟-18已被确立为一种有用的正电子发射同位素,可用于体内成像技术,这在药物发现和开发中可能有广泛应用,通常仅受限于标记化合物合成的便利性。氟在药物设计中的广泛应用为新合成方法的开发提供了强大动力,这些新方法能让人们更轻松地获得各种含氟化合物。在本综述中,我们提供了关于在药物分子中战略性引入氟的作用以及在正电子发射断层扫描中的应用的最新情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验