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本文引用的文献

1
Investigations into the Nature of Halogen Bonding Including Symmetry Adapted Perturbation Theory Analyses.关于卤素键本质的研究,包括对称性自适应微扰理论分析。
J Chem Theory Comput. 2008 Feb;4(2):232-42. doi: 10.1021/ct700216w.
2
Br···O Complexes as Probes of Factors Affecting Halogen Bonding: Interactions of Bromobenzenes and Bromopyrimidines with Acetone.作为影响卤键形成因素探针的溴……O配合物:溴苯和溴嘧啶与丙酮的相互作用
J Chem Theory Comput. 2009 Jan 13;5(1):155-63. doi: 10.1021/ct8004134. Epub 2008 Dec 18.
3
On Extension of the Current Biomolecular Empirical Force Field for the Description of Halogen Bonds.对当前生物分子经验力场的扩展以描述卤素键。
J Chem Theory Comput. 2012 Apr 10;8(4):1325-33. doi: 10.1021/ct2008389. Epub 2012 Mar 20.
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Scalable Anisotropic Shape and Electrostatic Models for Biological Bromine Halogen Bonds.用于生物溴卤键的可扩展各向异性形状和静电模型。
J Chem Theory Comput. 2012 Jul 10;8(7):2461-73. doi: 10.1021/ct3001969. Epub 2012 Jun 13.
5
Treatment of Halogen Bonding in the OPLS-AA Force Field; Application to Potent Anti-HIV Agents.OPLS-AA力场中卤键的处理;在强效抗HIV药物中的应用。
J Chem Theory Comput. 2012 Oct 9;8(10):3895-3801. doi: 10.1021/ct300180w. Epub 2012 Apr 3.
6
Discovery of novel allosteric mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors possessing bidentate Ser212 interactions.发现新型变构丝裂原活化蛋白激酶激酶(MEK)1、2 抑制剂,具有双齿 Ser212 相互作用。
J Med Chem. 2012 May 24;55(10):4594-604. doi: 10.1021/jm2017094. Epub 2012 May 3.
7
Halogen-enriched fragment libraries as leads for drug rescue of mutant p53.富含卤素的片段文库作为拯救突变型 p53 药物的先导物。
J Am Chem Soc. 2012 Apr 18;134(15):6810-8. doi: 10.1021/ja301056a. Epub 2012 Apr 5.
8
AMBER empirical potential describes the geometry and energy of noncovalent halogen interactions better than advanced semiempirical quantum mechanical method PM6-DH2X.AMBER 经验势比高级半经验量子力学方法 PM6-DH2X 更能准确描述非共价卤键相互作用的几何形状和能量。
J Phys Chem B. 2012 Mar 22;116(11):3659-69. doi: 10.1021/jp3003905. Epub 2012 Mar 6.
9
Regioselective deiodination of thyroxine by iodothyronine deiodinase mimics: an unusual mechanistic pathway involving cooperative chalcogen and halogen bonding.碘代甲状腺原氨酸脱碘酶模拟物对甲状腺素的区域选择性脱碘:涉及协同的硫属元素和卤素键的不寻常的机制途径。
J Am Chem Soc. 2012 Mar 7;134(9):4269-79. doi: 10.1021/ja210478k. Epub 2012 Feb 22.
10
Halogen bonding at the active sites of human cathepsin L and MEK1 kinase: efficient interactions in different environments.人组织蛋白酶 L 和 MEK1 激酶活性部位的卤键相互作用:不同环境中的有效相互作用。
ChemMedChem. 2011 Nov 4;6(11):2048-54. doi: 10.1002/cmdc.201100353. Epub 2011 Sep 6.

卤素键(X 键):生物学视角。

Halogen bonding (X-bonding): a biological perspective.

机构信息

Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado 80523-1870, USA.

出版信息

Protein Sci. 2013 Feb;22(2):139-52. doi: 10.1002/pro.2201. Epub 2012 Dec 29.

DOI:10.1002/pro.2201
PMID:23225628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3588911/
Abstract

The concept of the halogen bond (or X-bond) has become recognized as contributing significantly to the specificity in recognition of a large class of halogenated compounds. The interaction is most easily understood as primarily an electrostatically driven molecular interaction, where an electropositive crown, or σ-hole, serves as a Lewis acid to attract a variety of electron-rich Lewis bases, in analogous fashion to a classic hydrogen bonding (H-bond) interaction. We present here a broad overview of X-bonds from the perspective of a biologist who may not be familiar with this recently rediscovered class of interactions and, consequently, may be interested in how they can be applied as a highly directional and specific component of the molecular toolbox. This overview includes a discussion for where X-bonds are found in biomolecular structures, and how their structure-energy relationships are studied experimentally and modeled computationally. In total, our understanding of these basic concepts will allow X-bonds to be incorporated into strategies for the rational design of new halogenated inhibitors against biomolecular targets or toward molecular engineering of new biological-based materials.

摘要

卤键(或 X 键)的概念已被认为对一大类卤化化合物的特异性识别有重要贡献。这种相互作用最容易被理解为主要是静电驱动的分子相互作用,其中正电冠或 σ 空穴作为路易斯酸,以类似于经典氢键(H 键)相互作用的方式吸引各种富电子路易斯碱。我们从可能不熟悉这种最近重新发现的相互作用类别的生物学家的角度,在这里广泛概述 X 键,因此可能有兴趣了解如何将它们作为分子工具包的高度定向和特定组成部分应用。本综述包括讨论 X 键在生物分子结构中的位置,以及它们的结构-能量关系如何通过实验和计算建模进行研究。总的来说,我们对这些基本概念的理解将使 X 键能够被纳入针对生物分子靶标的新型卤化抑制剂的合理设计或新型基于生物的材料的分子工程的策略中。