首页> 外文期刊>Chemistry Select >ss-Aminoalcohols as Potential Reactivators of Aged Sarin-/Soman-Inhibited Acetylcholinesterase
【24h】

ss-Aminoalcohols as Potential Reactivators of Aged Sarin-/Soman-Inhibited Acetylcholinesterase

机译:SS-氨基醇作为老年/soman抑制的乙酰胆碱酯酶的潜在反击剂

获取原文
获取原文并翻译 | 示例
           

摘要

Organophosphate nerve agents inhibit the enzyme acetylcholinesterase (AChE), which is involved in nerve signal transduction, by forming covalent adducts with its catalytic serine residue. AChE adducts with soman and sarin nerve agents undergo dealkylation, a process known as aging, within a few minutes and a few hours, respectively. This transformation is detrimental because it precludes reactivation of AChE with known oxime-based antidotes. Here, we designed a b-aminoalcohol molecule for aged AChE reactivation, using a multitiered computational approach. This approach includes highquality quantum mechanical/molecular mechanical calculations, providing reliable reactivation steps and energetics. The calculations suggest that the designed b-aminoalcohol can selectively reactivate aged sarin-/soman-inhibited AChE. Furthermore, unlike existing antidotes, the designed b-aminoalcohol lacks a permanent charge, making it potentially active in the central nervous system. The mechanistic insights of this study can help guide the development of new AChE reactivators with improved access to the central nervous system.
机译:通过形成与其催化丝氨酸残基的共价加合物,有机磷酸神经剂抑制参与神经信号转导的酶乙酰胆碱酯酶(ACHE)。与Soman和Sarin神经剂的疼痛加合物分别在几分钟和几个小时内经历了称为衰老的过程。这种转化是有害的,因为它阻止了与已知的基于氧电机的解毒剂对ACHE的重新激活。在这里,我们使用多层计算方法设计了一个用于老化的ACAE重新激活的B氨基醇分子。该方法包括高质量的量子机械/分子机械计算,提供可靠的重新激活步骤和能量学。计算表明,设计的B-氨基醇可以选择性地重新激活老化的沙林/SOMAN抑制的ACHE。此外,与现有的解毒剂不同,设计的B-氨基醇缺乏永久性电荷,使其在中枢神经系统中有可能活跃。这项研究的机械见解可以帮助指导新的疼痛反应剂的发展,并改善了中枢神经系统的访问。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号