{"title":"数据驱动的卟啉几何洞察:非平面性和芳香性分析的可解释人工智能。","authors":"Shachar Fite,Zeev Gross","doi":"10.1021/acs.jcim.5c00518","DOIUrl":null,"url":null,"abstract":"Porphyrins are involved in numerous and very different chemical and biological processes, due to the sensitivity of their application-relevant properties to subtle structural changes. Applying modern machine learning methodology is very appealing for discovering structure-activity relationships that can be used for design of tailor-made porphyrins for specific purposes. For achieving this goal, a high-quality set consisting of 425 metal porphyrins was established via curation of 7590 porphyrin structures from the Cambridge crystallographic database. Using data-driven techniques for analyzing nonplanarity and \"structural aromaticity\" allowed for validation of common knowledge in the field as well as discovery of new relations. Aromaticity was found to be influenced differently by distinct nonplanar distortions. Nonplanarity is more sensitive to macrocycle substitutions than to metal or axial ligand effects, while ruffled distortions are dominated by axial ligand size and metal properties. These findings offer new insights into structure-property relationships in porphyrins, providing a data-driven foundation for targeted synthesis to tune aromaticity and nonplanarity. Despite data set limitations, this work demonstrates the value of machine learning in uncovering complex chemical trends.","PeriodicalId":44,"journal":{"name":"Journal of Chemical Information and Modeling ","volume":"11 1","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Data-Driven Insights into Porphyrin Geometry: Interpretable AI for Non-Planarity and Aromaticity Analyses.\",\"authors\":\"Shachar Fite,Zeev Gross\",\"doi\":\"10.1021/acs.jcim.5c00518\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Porphyrins are involved in numerous and very different chemical and biological processes, due to the sensitivity of their application-relevant properties to subtle structural changes. Applying modern machine learning methodology is very appealing for discovering structure-activity relationships that can be used for design of tailor-made porphyrins for specific purposes. For achieving this goal, a high-quality set consisting of 425 metal porphyrins was established via curation of 7590 porphyrin structures from the Cambridge crystallographic database. Using data-driven techniques for analyzing nonplanarity and \\\"structural aromaticity\\\" allowed for validation of common knowledge in the field as well as discovery of new relations. Aromaticity was found to be influenced differently by distinct nonplanar distortions. Nonplanarity is more sensitive to macrocycle substitutions than to metal or axial ligand effects, while ruffled distortions are dominated by axial ligand size and metal properties. These findings offer new insights into structure-property relationships in porphyrins, providing a data-driven foundation for targeted synthesis to tune aromaticity and nonplanarity. Despite data set limitations, this work demonstrates the value of machine learning in uncovering complex chemical trends.\",\"PeriodicalId\":44,\"journal\":{\"name\":\"Journal of Chemical Information and Modeling \",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-04-20\",\"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://doi.org/10.1021/acs.jcim.5c00518\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Information and Modeling ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.jcim.5c00518","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Data-Driven Insights into Porphyrin Geometry: Interpretable AI for Non-Planarity and Aromaticity Analyses.
Porphyrins are involved in numerous and very different chemical and biological processes, due to the sensitivity of their application-relevant properties to subtle structural changes. Applying modern machine learning methodology is very appealing for discovering structure-activity relationships that can be used for design of tailor-made porphyrins for specific purposes. For achieving this goal, a high-quality set consisting of 425 metal porphyrins was established via curation of 7590 porphyrin structures from the Cambridge crystallographic database. Using data-driven techniques for analyzing nonplanarity and "structural aromaticity" allowed for validation of common knowledge in the field as well as discovery of new relations. Aromaticity was found to be influenced differently by distinct nonplanar distortions. Nonplanarity is more sensitive to macrocycle substitutions than to metal or axial ligand effects, while ruffled distortions are dominated by axial ligand size and metal properties. These findings offer new insights into structure-property relationships in porphyrins, providing a data-driven foundation for targeted synthesis to tune aromaticity and nonplanarity. Despite data set limitations, this work demonstrates the value of machine learning in uncovering complex chemical trends.
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.