• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用分子建模软件估算染料和荧光探针QSAR研究通用描述符的替代方法。2. log P与亲水/亲脂指数之间的相关性以及估算两亲性程度的新方法。

Alternative methods for estimating common descriptors for QSAR studies of dyes and fluorescent probes using molecular modeling software. 2. Correlations between log P and the hydrophilic/lipophilic index, and new methods for estimating degrees of amphiphilicity.

作者信息

Dapson Richard W, Horobin Richard W

机构信息

Dapson & Dapson, LLC , 6951 East AB Avenue, Richland, Michigan.

出版信息

Biotech Histochem. 2013 Nov;88(8):489-97. doi: 10.3109/10520295.2013.811287. Epub 2013 Aug 1.

DOI:10.3109/10520295.2013.811287
PMID:23901949
Abstract

The log P descriptor, despite its usefulness, can be difficult to use, especially for researchers lacking skills in physical chemistry. Moreover this classic measure has been determined in numerous ways, which can result in inconsistant estimates of log P values, especially for relatively complex molecules such as fluorescent probes. Novel measures of hydrophilicity/lipophilicity (the Hydrophilic/Lipophilic Index, HLI) and amphiphilicity (hydrophilic/lipophilic indices for the head group and tail, HLIT and HLIHG, respectively) therefore have been devised. We compare these descriptors with measures based on log P, the standard method for quantitative structure activity relationships (QSAR) studies. HLI can be determined using widely available molecular modeling software, coupled with simple arithmetic calculations. It is based on partial atomic charges and is intended to be a stand-alone measure of hydrophilicity/lipophilicity. Given the wide application of log P, however, we investigated the correlation between HLI and log P using a test set of 56 fluorescent probes of widely different physicochemical character. Overall correlation was poor; however, correlation of HLI and log P for probes of narrowly specified charge types, i.e., non-ionic compounds, anions, conjugated cations, or zwitterions, was excellent. Values for probes with additional nonconjugated quaternary cations, however, were less well correlated. The newly devised HLI can be divided into domain-specific descriptors, HLIT and HLIHG in amphiphilic probes. Determinations of amphiphilicity, made independently by the authors using their respective methods, showed excellent agreement. Quantifying amphiphilicity from partial log P values of the head group (head group hydrophilicity; HGH) and tail (amphiphilicity index; AI) has proved useful for understanding fluorescent probe action. The same limitations of log P apply to HGH and AI, however. The novel descriptors, HLIT and HLIHG, offer analogous advantages to those seen with HLI over log P. The high correlation between log P and HLI, and the concordance between the two systems for assessing amphiphilicity, provide a powerful tool for QSAR studies. It is possible now to select a probe with missing fragments, and thus no log P, AI or HGH; and to estimate these important descriptors from parameters derived from HLI.

摘要

尽管log P描述符很有用,但使用起来可能很困难,尤其是对于缺乏物理化学技能的研究人员。此外,这种经典的测量方法有多种确定方式,这可能导致log P值的估计不一致,特别是对于荧光探针等相对复杂的分子。因此,人们设计了亲水性/亲脂性的新测量方法(亲水/亲脂指数,HLI)和两亲性(分别针对头部基团和尾部基团的亲水/亲脂指数,HLIT和HLIHG)。我们将这些描述符与基于log P的测量方法进行比较,log P是定量构效关系(QSAR)研究的标准方法。HLI可以使用广泛可用的分子建模软件并结合简单的算术计算来确定。它基于部分原子电荷,旨在作为亲水性/亲脂性的独立测量方法。然而,鉴于log P的广泛应用,我们使用一组56种具有广泛不同物理化学性质的荧光探针测试集研究了HLI与log P之间的相关性。总体相关性较差;然而,对于特定电荷类型的探针,即非离子化合物、阴离子、共轭阳离子或两性离子,HLI与log P的相关性非常好。然而,具有额外非共轭季铵阳离子的探针的值相关性较差。新设计的HLI可以分为两亲性探针中特定域的描述符HLIT和HLIHG。作者使用各自的方法独立进行的两亲性测定显示出极好的一致性。从头部基团(头部基团亲水性;HGH)和尾部(两亲性指数;AI)的部分log P值量化两亲性已被证明有助于理解荧光探针的作用。然而,log P的同样局限性也适用于HGH和AI。新颖的描述符HLIT和HLIHG与HLI相比log P具有类似的优势。log P与HLI之间的高度相关性以及两个评估两亲性系统之间的一致性为QSAR研究提供了一个强大的工具。现在有可能选择一个缺少片段,因此没有log P、AI或HGH的探针;并从HLI导出的参数估计这些重要描述符。

相似文献

1
Alternative methods for estimating common descriptors for QSAR studies of dyes and fluorescent probes using molecular modeling software. 2. Correlations between log P and the hydrophilic/lipophilic index, and new methods for estimating degrees of amphiphilicity.使用分子建模软件估算染料和荧光探针QSAR研究通用描述符的替代方法。2. log P与亲水/亲脂指数之间的相关性以及估算两亲性程度的新方法。
Biotech Histochem. 2013 Nov;88(8):489-97. doi: 10.3109/10520295.2013.811287. Epub 2013 Aug 1.
2
Alternative methods for estimating common descriptors for QSAR studies of dyes and fluorescent probes using molecular modeling software: 1. Concepts and procedures.使用分子建模软件估算染料和荧光探针的QSAR研究通用描述符的替代方法:1. 概念与程序。
Biotech Histochem. 2013 Nov;88(8):477-88. doi: 10.3109/10520295.2013.811286. Epub 2013 Aug 1.
3
Predicting small molecule fluorescent probe localization in living cells using QSAR modeling. 2. Specifying probe, protocol and cell factors; selecting QSAR models; predicting entry and localization.使用定量构效关系(QSAR)建模预测小分子荧光探针在活细胞中的定位。2. 确定探针、实验方案和细胞因素;选择QSAR模型;预测进入和定位情况。
Biotech Histochem. 2013 Nov;88(8):461-76. doi: 10.3109/10520295.2013.780635. Epub 2013 Jun 13.
4
Uptake and localization mechanisms of fluorescent and colored lipid probes. 1. Physicochemistry of probe uptake and localization, and the use of QSAR models for selectivity prediction.荧光和有色脂质探针的摄取与定位机制。1. 探针摄取与定位的物理化学性质,以及定量构效关系模型在选择性预测中的应用。
Biotech Histochem. 2011 Dec;86(6):379-93. doi: 10.3109/10520295.2010.515489. Epub 2010 Sep 6.
5
Identifying apoptotic cells with the 3-hydroxyflavone derivative F2N12S, a ratiometric fluorescent small molecule probe selective for plasma membranes: a possible general mechanism for selective uptake into apoptotic cells.用3-羟基黄酮衍生物F2N12S鉴定凋亡细胞,F2N12S是一种对质膜具有选择性的比率荧光小分子探针:这是一种可能的选择性摄取进入凋亡细胞的普遍机制。
Biotech Histochem. 2011 Aug;86(4):255-61. doi: 10.3109/10520291003723426. Epub 2010 Apr 6.
6
Fluorescent cationic probes for nuclei of living cells: why are they selective? A quantitative structure-activity relations analysis.用于活细胞核的荧光阳离子探针:它们为何具有选择性?定量构效关系分析。
Histochem Cell Biol. 2006 Aug;126(2):165-75. doi: 10.1007/s00418-006-0156-7. Epub 2006 Feb 7.
7
Selective labeling of lipid droplets in aldehyde fixed cell monolayers by lipophilic fluorochromes.通过亲脂性荧光染料对醛固定细胞单层中的脂滴进行选择性标记。
Biotech Histochem. 2010 Oct;85(5):277-83. doi: 10.3109/10520290903196183.
8
How to Target Small-Molecule Fluorescent Imaging Probes to the Plasma Membrane-The Influence and QSAR Modelling of Amphiphilicity, Lipophilicity, and Flip-Flop.如何将小分子荧光成像探针靶向质膜——两亲性、亲脂性和翻转的影响及定量构效关系建模。
Molecules. 2023 Nov 14;28(22):7589. doi: 10.3390/molecules28227589.
9
Some molecular descriptors for non-specific chromosomal genotoxicity based on hydrophobic interactions.基于疏水相互作用的非特异性染色体遗传毒性的一些分子描述符。
Arch Toxicol. 2008 May;82(5):333-8. doi: 10.1007/s00204-007-0256-8. Epub 2007 Nov 9.
10
Predicting small molecule fluorescent probe localization in living cells using QSAR modeling. 1. Overview and models for probes of structure, properties and function in single cells.使用定量构效关系(QSAR)建模预测小分子荧光探针在活细胞中的定位。1. 单细胞中结构、性质和功能探针的概述及模型
Biotech Histochem. 2013 Nov;88(8):440-60. doi: 10.3109/10520295.2013.780634. Epub 2013 Jun 13.

引用本文的文献

1
Benchmark of different charges for prediction of the partitioning coefficient through the hydrophilic/lipophilic index.通过亲水/亲脂性指数预测分配系数的不同电荷基准。
J Mol Model. 2018 May 31;24(6):141. doi: 10.1007/s00894-018-3692-x.