Molecular Field Extrema as Descriptors of Biological Activity: Definition and Validation
The paper describes the generation of four types of three-dimensional molecular field descriptors or ‘field points' as extrema of electrostatic, steric, and hydrophobic fields. These field points are used to define the properties necessary for a molecule to bind in a characteristic way into a s...
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Veröffentlicht in: | Journal of chemical information and modeling 2006-03, Vol.46 (2), p.665-676 |
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creator | Cheeseright, Tim Mackey, Mark Rose, Sally Vinter, Andy |
description | The paper describes the generation of four types of three-dimensional molecular field descriptors or ‘field points' as extrema of electrostatic, steric, and hydrophobic fields. These field points are used to define the properties necessary for a molecule to bind in a characteristic way into a specified active site. The hypothesis is that compounds showing a similar field point pattern are likely to bind at the same target site regardless of structure. The methodology to test this idea is illustrated using HIV NNRTI and thrombin ligands and validated across seven other targets. From the in silico comparisons of field point overlays, the experimentally observed binding poses of these ligands in their respective sites can be reproduced from pairwise comparisons. |
doi_str_mv | 10.1021/ci050357s |
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From the in silico comparisons of field point overlays, the experimentally observed binding poses of these ligands in their respective sites can be reproduced from pairwise comparisons.</description><identifier>ISSN: 1549-9596</identifier><identifier>EISSN: 1549-960X</identifier><identifier>DOI: 10.1021/ci050357s</identifier><identifier>PMID: 16562997</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Algorithms ; Anti-HIV Agents - chemistry ; Drug Design ; Models, Biological ; Models, Chemical ; Molecular biology ; Molecular Conformation ; Molecular Structure ; Structure-Activity Relationship ; Thrombin - antagonists & inhibitors</subject><ispartof>Journal of chemical information and modeling, 2006-03, Vol.46 (2), p.665-676</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>Copyright American Chemical Society Mar 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a308t-bf28508a86fbdca4d5b8e45b3adf66e50984924f3146aa5bbf97e9b723801163</citedby><cites>FETCH-LOGICAL-a308t-bf28508a86fbdca4d5b8e45b3adf66e50984924f3146aa5bbf97e9b723801163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ci050357s$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ci050357s$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2751,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16562997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheeseright, Tim</creatorcontrib><creatorcontrib>Mackey, Mark</creatorcontrib><creatorcontrib>Rose, Sally</creatorcontrib><creatorcontrib>Vinter, Andy</creatorcontrib><title>Molecular Field Extrema as Descriptors of Biological Activity: Definition and Validation</title><title>Journal of chemical information and modeling</title><addtitle>J. Chem. Inf. Model</addtitle><description>The paper describes the generation of four types of three-dimensional molecular field descriptors or ‘field points' as extrema of electrostatic, steric, and hydrophobic fields. These field points are used to define the properties necessary for a molecule to bind in a characteristic way into a specified active site. The hypothesis is that compounds showing a similar field point pattern are likely to bind at the same target site regardless of structure. The methodology to test this idea is illustrated using HIV NNRTI and thrombin ligands and validated across seven other targets. From the in silico comparisons of field point overlays, the experimentally observed binding poses of these ligands in their respective sites can be reproduced from pairwise comparisons.</description><subject>Algorithms</subject><subject>Anti-HIV Agents - chemistry</subject><subject>Drug Design</subject><subject>Models, Biological</subject><subject>Models, Chemical</subject><subject>Molecular biology</subject><subject>Molecular Conformation</subject><subject>Molecular Structure</subject><subject>Structure-Activity Relationship</subject><subject>Thrombin - antagonists & inhibitors</subject><issn>1549-9596</issn><issn>1549-960X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpl0E1rFDEYB_BQLH2zB7-ABMGCh9G8TJJJb-3abZX6Al1E8BCeySSSmp2syYy0N69-TT-JU3ZtQU9JeH48-fNH6AklLylh9JUNRBAuVNlCe1TUutKSfH709y603EX7pVwTwrmWbAftUikk01rtoS_vUnR2jJDxPLjY4bObIbslYCj4tSs2h9WQcsHJ49OQYvoaLER8YofwIwy3x79__pqYD30YQuox9B3-BDF0cPd8jLY9xOION-cBWszPFrOL6vLD-ZvZyWUFnDRD1XrWCNJAI33bWag70TauFi2HzkvpBNFNrVntOa0lgGhbr5XTrWK8IZRKfoCO1mtXOX0fXRnMMhTrYoTepbEYqZRmUqsJPvsHXqcx91M0w6hkXKtaTOjFGtmcSsnOm1UOS8i3hhJz17a5b3uyTzcLx3bpuge5qXcC1RqEMrib-znkb1MqroRZfLwycyVnp2-bC_N-8s_XHmx5CPf_x38Ae-2V1w</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Cheeseright, Tim</creator><creator>Mackey, Mark</creator><creator>Rose, Sally</creator><creator>Vinter, Andy</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SC</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>7X8</scope></search><sort><creationdate>20060301</creationdate><title>Molecular Field Extrema as Descriptors of Biological Activity: Definition and Validation</title><author>Cheeseright, Tim ; Mackey, Mark ; Rose, Sally ; Vinter, Andy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a308t-bf28508a86fbdca4d5b8e45b3adf66e50984924f3146aa5bbf97e9b723801163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Algorithms</topic><topic>Anti-HIV Agents - chemistry</topic><topic>Drug Design</topic><topic>Models, Biological</topic><topic>Models, Chemical</topic><topic>Molecular biology</topic><topic>Molecular Conformation</topic><topic>Molecular Structure</topic><topic>Structure-Activity Relationship</topic><topic>Thrombin - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheeseright, Tim</creatorcontrib><creatorcontrib>Mackey, Mark</creatorcontrib><creatorcontrib>Rose, Sally</creatorcontrib><creatorcontrib>Vinter, Andy</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Computer and Information Systems Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of chemical information and modeling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheeseright, Tim</au><au>Mackey, Mark</au><au>Rose, Sally</au><au>Vinter, Andy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Field Extrema as Descriptors of Biological Activity: Definition and Validation</atitle><jtitle>Journal of chemical information and modeling</jtitle><addtitle>J. Chem. Inf. Model</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>46</volume><issue>2</issue><spage>665</spage><epage>676</epage><pages>665-676</pages><issn>1549-9596</issn><eissn>1549-960X</eissn><abstract>The paper describes the generation of four types of three-dimensional molecular field descriptors or ‘field points' as extrema of electrostatic, steric, and hydrophobic fields. These field points are used to define the properties necessary for a molecule to bind in a characteristic way into a specified active site. The hypothesis is that compounds showing a similar field point pattern are likely to bind at the same target site regardless of structure. The methodology to test this idea is illustrated using HIV NNRTI and thrombin ligands and validated across seven other targets. 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source | MEDLINE; American Chemical Society Journals |
subjects | Algorithms Anti-HIV Agents - chemistry Drug Design Models, Biological Models, Chemical Molecular biology Molecular Conformation Molecular Structure Structure-Activity Relationship Thrombin - antagonists & inhibitors |
title | Molecular Field Extrema as Descriptors of Biological Activity: Definition and Validation |
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