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Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases
Alzheimer’s disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and Aβ species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics direc...
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Published in: | Journal of medicinal chemistry 2017-06, Vol.60 (12), p.5120-5145 |
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creator | Cornec, Anne-Sophie Monti, Ludovica Kovalevich, Jane Makani, Vishruti James, Michael J Vijayendran, Krishna G Oukoloff, Killian Yao, Yuemang Lee, Virginia M.-Y Trojanowski, John Q Smith, Amos B Brunden, Kurt R Ballatore, Carlo |
description | Alzheimer’s disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and Aβ species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure–activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. Several examples are brain-penetrant and exhibit balanced multitargeted in vitro activity in the low μM range. As brain-penetrant MT-stabilizing agents have proven effective against tau-mediated neurodegeneration in animal models, and because COX- and 5-LOX-derived eicosanoids are thought to contribute to Aβ plaque deposition, these 1,5-diarylimidazoles provide tools to explore novel multitargeted strategies for AD and other neurodegenerative diseases. |
doi_str_mv | 10.1021/acs.jmedchem.7b00475 |
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In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure–activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. Several examples are brain-penetrant and exhibit balanced multitargeted in vitro activity in the low μM range. As brain-penetrant MT-stabilizing agents have proven effective against tau-mediated neurodegeneration in animal models, and because COX- and 5-LOX-derived eicosanoids are thought to contribute to Aβ plaque deposition, these 1,5-diarylimidazoles provide tools to explore novel multitargeted strategies for AD and other neurodegenerative diseases.</description><identifier>ISSN: 0022-2623</identifier><identifier>EISSN: 1520-4804</identifier><identifier>DOI: 10.1021/acs.jmedchem.7b00475</identifier><identifier>PMID: 28530811</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Alzheimer Disease - drug therapy ; Animals ; Arachidonate 5-Lipoxygenase - metabolism ; Chemistry Techniques, Synthetic ; Cyclooxygenase Inhibitors - chemistry ; Cyclooxygenase Inhibitors - pharmacology ; Drug Evaluation, Preclinical - methods ; Female ; Humans ; Imidazoles - chemistry ; Imidazoles - pharmacology ; Leukotrienes - biosynthesis ; Lipoxygenase Inhibitors - chemistry ; Lipoxygenase Inhibitors - pharmacology ; Male ; Mice, Inbred Strains ; Microtubules - drug effects ; Microtubules - metabolism ; Molecular Targeted Therapy ; Neurodegenerative Diseases - drug therapy ; Prostaglandins - metabolism ; Rats ; Structure-Activity Relationship</subject><ispartof>Journal of medicinal chemistry, 2017-06, Vol.60 (12), p.5120-5145</ispartof><rights>Copyright © 2017 American Chemical Society</rights><rights>Copyright © 2017 American Chemical Society 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a449t-3357bdce08ef4a780e42fa4e663816a7e7e1413be70d3ea053f0062569a7e5853</citedby><cites>FETCH-LOGICAL-a449t-3357bdce08ef4a780e42fa4e663816a7e7e1413be70d3ea053f0062569a7e5853</cites><orcidid>0000-0002-2718-3850 ; 0000-0002-1712-8567</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28530811$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cornec, Anne-Sophie</creatorcontrib><creatorcontrib>Monti, Ludovica</creatorcontrib><creatorcontrib>Kovalevich, Jane</creatorcontrib><creatorcontrib>Makani, Vishruti</creatorcontrib><creatorcontrib>James, Michael J</creatorcontrib><creatorcontrib>Vijayendran, Krishna G</creatorcontrib><creatorcontrib>Oukoloff, Killian</creatorcontrib><creatorcontrib>Yao, Yuemang</creatorcontrib><creatorcontrib>Lee, Virginia M.-Y</creatorcontrib><creatorcontrib>Trojanowski, John Q</creatorcontrib><creatorcontrib>Smith, Amos B</creatorcontrib><creatorcontrib>Brunden, Kurt R</creatorcontrib><creatorcontrib>Ballatore, Carlo</creatorcontrib><title>Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases</title><title>Journal of medicinal chemistry</title><addtitle>J. Med. Chem</addtitle><description>Alzheimer’s disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and Aβ species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure–activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. Several examples are brain-penetrant and exhibit balanced multitargeted in vitro activity in the low μM range. As brain-penetrant MT-stabilizing agents have proven effective against tau-mediated neurodegeneration in animal models, and because COX- and 5-LOX-derived eicosanoids are thought to contribute to Aβ plaque deposition, these 1,5-diarylimidazoles provide tools to explore novel multitargeted strategies for AD and other neurodegenerative diseases.</description><subject>Alzheimer Disease - drug therapy</subject><subject>Animals</subject><subject>Arachidonate 5-Lipoxygenase - metabolism</subject><subject>Chemistry Techniques, Synthetic</subject><subject>Cyclooxygenase Inhibitors - chemistry</subject><subject>Cyclooxygenase Inhibitors - pharmacology</subject><subject>Drug Evaluation, Preclinical - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Imidazoles - chemistry</subject><subject>Imidazoles - pharmacology</subject><subject>Leukotrienes - biosynthesis</subject><subject>Lipoxygenase Inhibitors - chemistry</subject><subject>Lipoxygenase Inhibitors - pharmacology</subject><subject>Male</subject><subject>Mice, Inbred Strains</subject><subject>Microtubules - drug effects</subject><subject>Microtubules - metabolism</subject><subject>Molecular Targeted Therapy</subject><subject>Neurodegenerative Diseases - drug therapy</subject><subject>Prostaglandins - metabolism</subject><subject>Rats</subject><subject>Structure-Activity Relationship</subject><issn>0022-2623</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kctuFDEQRS0EIkPgDxDykk1Pyo9-DAukKCQk0kBYhLVV010948jdHmx3JLLKb-T3-BIcZhLBhlUt6t5bj8PYWwFzAVIcYRvn1wN17YaGeb0C0HX5jM1EKaHQDejnbAYgZSErqQ7YqxivAUAJqV6yA9mUChohZsx9mVyyCcOaEnX8YrAd3npH8QP_5hONyaLjVxsKuKUp2ZYvCbvIex_4sbvdkB0o_Lq7jxzHjl-mLORfaQq-ozWN2ZXsDfFPNhJGiq_Zix5dpDf7esi-n51enZwXy8vPFyfHywK1XqRCqbJedS1BQ73GugHSskdNVaUaUWFNNQkt1Ipq6BQhlKoHqGRZLXKvzKcdso-73O20evhQPiOgM9tgBww_jUdr_u2MdmPW_saUulHNQuWA9_uA4H9MFJMZbGzJORzJT9GIBYi61FUlslTvpG3wMQbqn8YIMA-gTAZlHkGZPahse_f3ik-mRzJZADvBH7ufwpg_9v_M37PNpl4</recordid><startdate>20170622</startdate><enddate>20170622</enddate><creator>Cornec, Anne-Sophie</creator><creator>Monti, Ludovica</creator><creator>Kovalevich, Jane</creator><creator>Makani, Vishruti</creator><creator>James, Michael J</creator><creator>Vijayendran, Krishna G</creator><creator>Oukoloff, Killian</creator><creator>Yao, Yuemang</creator><creator>Lee, Virginia M.-Y</creator><creator>Trojanowski, John Q</creator><creator>Smith, Amos B</creator><creator>Brunden, Kurt R</creator><creator>Ballatore, Carlo</creator><general>American Chemical Society</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2718-3850</orcidid><orcidid>https://orcid.org/0000-0002-1712-8567</orcidid></search><sort><creationdate>20170622</creationdate><title>Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases</title><author>Cornec, Anne-Sophie ; Monti, Ludovica ; Kovalevich, Jane ; Makani, Vishruti ; James, Michael J ; Vijayendran, Krishna G ; Oukoloff, Killian ; Yao, Yuemang ; Lee, Virginia M.-Y ; Trojanowski, John Q ; Smith, Amos B ; Brunden, Kurt R ; Ballatore, Carlo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a449t-3357bdce08ef4a780e42fa4e663816a7e7e1413be70d3ea053f0062569a7e5853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Alzheimer Disease - drug therapy</topic><topic>Animals</topic><topic>Arachidonate 5-Lipoxygenase - metabolism</topic><topic>Chemistry Techniques, Synthetic</topic><topic>Cyclooxygenase Inhibitors - chemistry</topic><topic>Cyclooxygenase Inhibitors - pharmacology</topic><topic>Drug Evaluation, Preclinical - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Imidazoles - chemistry</topic><topic>Imidazoles - pharmacology</topic><topic>Leukotrienes - biosynthesis</topic><topic>Lipoxygenase Inhibitors - chemistry</topic><topic>Lipoxygenase Inhibitors - pharmacology</topic><topic>Male</topic><topic>Mice, Inbred Strains</topic><topic>Microtubules - drug effects</topic><topic>Microtubules - metabolism</topic><topic>Molecular Targeted Therapy</topic><topic>Neurodegenerative Diseases - drug therapy</topic><topic>Prostaglandins - metabolism</topic><topic>Rats</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cornec, Anne-Sophie</creatorcontrib><creatorcontrib>Monti, Ludovica</creatorcontrib><creatorcontrib>Kovalevich, Jane</creatorcontrib><creatorcontrib>Makani, Vishruti</creatorcontrib><creatorcontrib>James, Michael J</creatorcontrib><creatorcontrib>Vijayendran, Krishna G</creatorcontrib><creatorcontrib>Oukoloff, Killian</creatorcontrib><creatorcontrib>Yao, Yuemang</creatorcontrib><creatorcontrib>Lee, Virginia M.-Y</creatorcontrib><creatorcontrib>Trojanowski, John Q</creatorcontrib><creatorcontrib>Smith, Amos B</creatorcontrib><creatorcontrib>Brunden, Kurt R</creatorcontrib><creatorcontrib>Ballatore, Carlo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cornec, Anne-Sophie</au><au>Monti, Ludovica</au><au>Kovalevich, Jane</au><au>Makani, Vishruti</au><au>James, Michael J</au><au>Vijayendran, Krishna G</au><au>Oukoloff, Killian</au><au>Yao, Yuemang</au><au>Lee, Virginia M.-Y</au><au>Trojanowski, John Q</au><au>Smith, Amos B</au><au>Brunden, Kurt R</au><au>Ballatore, Carlo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>2017-06-22</date><risdate>2017</risdate><volume>60</volume><issue>12</issue><spage>5120</spage><epage>5145</epage><pages>5120-5145</pages><issn>0022-2623</issn><eissn>1520-4804</eissn><abstract>Alzheimer’s disease (AD) is a complex, multifactorial disease in which different neuropathological mechanisms are likely involved, including those associated with pathological tau and Aβ species as well as neuroinflammation. In this context, the development of single multitargeted therapeutics directed against two or more disease mechanisms could be advantageous. Starting from a series of 1,5-diarylimidazoles with microtubule (MT)-stabilizing activity and structural similarities with known NSAIDs, we conducted structure–activity relationship studies that led to the identification of multitargeted prototypes with activities as MT-stabilizing agents and/or inhibitors of the cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) pathways. 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subjects | Alzheimer Disease - drug therapy Animals Arachidonate 5-Lipoxygenase - metabolism Chemistry Techniques, Synthetic Cyclooxygenase Inhibitors - chemistry Cyclooxygenase Inhibitors - pharmacology Drug Evaluation, Preclinical - methods Female Humans Imidazoles - chemistry Imidazoles - pharmacology Leukotrienes - biosynthesis Lipoxygenase Inhibitors - chemistry Lipoxygenase Inhibitors - pharmacology Male Mice, Inbred Strains Microtubules - drug effects Microtubules - metabolism Molecular Targeted Therapy Neurodegenerative Diseases - drug therapy Prostaglandins - metabolism Rats Structure-Activity Relationship |
title | Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer’s and Other Neurodegenerative Diseases |
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