QSAR as a Small-Deformation Theory of Effective Free-Energy Landscapes

IF 6.4 2区 化学 Q1 CHEMISTRY, MEDICINAL
Jun-ichi Okada, Katsuhito Fujiu
{"title":"QSAR as a Small-Deformation Theory of Effective Free-Energy Landscapes","authors":"Jun-ichi Okada,&nbsp;Katsuhito Fujiu","doi":"10.1021/acs.jcim.6c01230","DOIUrl":null,"url":null,"abstract":"<p>Quantitative structure–activity relationships\r\n(QSARs) remain\r\nwidely used in medicinal chemistry, yet their physical interpretation\r\nis often limited and the meaning of their applicability domain (AD)\r\nis commonly treated in statistical or descriptor-space terms. Here\r\nwe propose a conceptual framework in which QSAR is interpreted as\r\na small-deformation theory of effective free-energy landscapes. Ligand\r\nbinding or chemical substitution is represented as a perturbation\r\nof an effective free-energy landscape defined over reduced state variables,\r\nand the resulting free-energy response is expressed as a contracted\r\nobservable over the equilibrium ensemble of the reference system via\r\na Zwanzig-type perturbation formula. At the phenomenological level,\r\nthis response reduces to a low-order expansion in descriptor space,\r\nfrom which conventional linear QSAR emerges as the leading-order approximation.\r\nWithin the assumed effective description and under stated regularity\r\nconditions, the corresponding first-order coefficients are given exactly\r\nby the ensemble-averaged sensitivities of the free-energy landscape\r\nto descriptor perturbations, without requiring a cumulant truncation.\r\nThe AD acquires a physical meaning as the region in which a local\r\nlow-order expansion of the free-energy response remains valid. In\r\nthe small-deformation regime, this same region further corresponds\r\nto ligand-induced landscape perturbations that remain local, smooth,\r\nand sufficiently weak over the reference ensemble. Conversely, in\r\nsystems for which an effective-landscape description is appropriate,\r\nQSAR breakdown may be associated with phenomena such as activity cliffs,\r\ninduced fit, and state-dependent binding, which can involve qualitative\r\nreorganization or rapid reweighting of the effective landscape. For\r\na specified thermodynamic system, the second-cumulant term provides\r\na non-positive variance correction to the leading-order ensemble-average\r\nfree-energy response, arising from the variance of the landscape perturbation\r\nover the reference ensemble. This correction reflects a fluctuation-assisted\r\neffect in which configurational heterogeneity within the pre-existing\r\nensemble allows Boltzmann reweighting to redistribute statistical\r\nweight toward microstates more strongly influenced by the perturbation.\r\nIndependently, the exact free-energy response is no greater than the\r\nleading-order ensemble-average estimate, consistent with Jensen’s\r\ninequality. The present framework is conceptual. Its interpretation\r\nof QSAR coefficients as ensemble-averaged sensitivities of the free-energy\r\nlandscape requires additional assumptions and state-resolved information\r\nbeyond conventional compound-level QSAR data, and it does not by itself\r\nprovide a prospective AD method.</p>","PeriodicalId":44,"journal":{"name":"Journal of Chemical Information and Modeling ","volume":"66 19","pages":"12576–12586"},"PeriodicalIF":6.4000,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Information and Modeling ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jcim.6c01230","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/9 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Quantitative structure–activity relationships (QSARs) remain widely used in medicinal chemistry, yet their physical interpretation is often limited and the meaning of their applicability domain (AD) is commonly treated in statistical or descriptor-space terms. Here we propose a conceptual framework in which QSAR is interpreted as a small-deformation theory of effective free-energy landscapes. Ligand binding or chemical substitution is represented as a perturbation of an effective free-energy landscape defined over reduced state variables, and the resulting free-energy response is expressed as a contracted observable over the equilibrium ensemble of the reference system via a Zwanzig-type perturbation formula. At the phenomenological level, this response reduces to a low-order expansion in descriptor space, from which conventional linear QSAR emerges as the leading-order approximation. Within the assumed effective description and under stated regularity conditions, the corresponding first-order coefficients are given exactly by the ensemble-averaged sensitivities of the free-energy landscape to descriptor perturbations, without requiring a cumulant truncation. The AD acquires a physical meaning as the region in which a local low-order expansion of the free-energy response remains valid. In the small-deformation regime, this same region further corresponds to ligand-induced landscape perturbations that remain local, smooth, and sufficiently weak over the reference ensemble. Conversely, in systems for which an effective-landscape description is appropriate, QSAR breakdown may be associated with phenomena such as activity cliffs, induced fit, and state-dependent binding, which can involve qualitative reorganization or rapid reweighting of the effective landscape. For a specified thermodynamic system, the second-cumulant term provides a non-positive variance correction to the leading-order ensemble-average free-energy response, arising from the variance of the landscape perturbation over the reference ensemble. This correction reflects a fluctuation-assisted effect in which configurational heterogeneity within the pre-existing ensemble allows Boltzmann reweighting to redistribute statistical weight toward microstates more strongly influenced by the perturbation. Independently, the exact free-energy response is no greater than the leading-order ensemble-average estimate, consistent with Jensen’s inequality. The present framework is conceptual. Its interpretation of QSAR coefficients as ensemble-averaged sensitivities of the free-energy landscape requires additional assumptions and state-resolved information beyond conventional compound-level QSAR data, and it does not by itself provide a prospective AD method.

QSAR:有效自由能景观的小变形理论
定量构效关系(qsar)仍然广泛应用于药物化学,但其物理解释往往是有限的,其适用域(AD)的含义通常用统计或描述空间术语来处理。在这里,我们提出了一个概念框架,其中QSAR被解释为有效自由能景观的小变形理论。配体结合或化学取代被表示为在简化状态变量上定义的有效自由能景观的扰动,由此产生的自由能响应通过zwanzig型扰动公式表示为参考系统平衡系综上的收缩观测值。在现象学水平上,这种响应降低到描述符空间中的低阶展开,由此传统的线性QSAR作为首阶近似出现。在假设的有效描述和规定的正则性条件下,相应的一阶系数由自由能景观对描述扰动的集合平均灵敏度精确给出,而不需要累积截断。AD具有物理意义,即自由能响应的局部低阶展开仍然有效的区域。在小变形状态下,这个区域进一步对应于配体引起的景观扰动,这些扰动在参考系综上保持局部、光滑和足够弱。相反,在有效景观描述合适的系统中,QSAR分解可能与活动悬崖、诱导拟合和状态依赖结合等现象有关,这些现象可能涉及有效景观的定性重组或快速重加权。对于一个特定的热力学系统,第二次累积项提供了一个非正方差校正的领先级系综平均自由能响应,由景观扰动对参考系综的方差引起。这种修正反映了一种波动辅助效应,在这种效应中,预先存在的系综中的构型异质性允许玻尔兹曼重加权,将统计权重重新分配给受扰动影响更强的微观状态。独立地,精确的自由能响应不大于首阶总体平均估计,与詹森不等式一致。目前的框架是概念性的。它将QSAR系数解释为自由能景观的整体平均灵敏度,需要额外的假设和状态分辨信息,而不是传统的化合物水平QSAR数据,而且它本身并不能提供一个有前景的AD方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书