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Natural sesquiterpenoid oligomers: A chemical perspective
Sesquiterpenoid oligomers, biogenetically assembled by at least two monomeric sesquiterpenoid units via diverse pathways, represent a unique class of natural products with distinct bioactivities. Herein, we provide a review covering the dimeric, trimeric, and tetrameric sesquiterpenoids categorized...
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Published in: | European journal of medicinal chemistry 2020-10, Vol.203, p.112622-112622, Article 112622 |
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container_title | European journal of medicinal chemistry |
container_volume | 203 |
creator | Zhao, Wen-Yu Yan, Juan-Juan Liu, Tian-Tian Gao, Jian Huang, Hui-Lian Sun, Cheng-Peng Huo, Xiao-Kui Deng, Sa Zhang, Bao-Jing Ma, Xiao-Chi |
description | Sesquiterpenoid oligomers, biogenetically assembled by at least two monomeric sesquiterpenoid units via diverse pathways, represent a unique class of natural products with distinct bioactivities. Herein, we provide a review covering the dimeric, trimeric, and tetrameric sesquiterpenoids categorized by reaction types in biosynthesis from a chemical perspective. Emphasis is focused on the biosynthetic oligomerization pathways of these interesting molecules and their related biological functions, which will supply inspiration for the total synthesis or biomimetic synthesis of more oligomeric sesquiterpenoids and further pharmacological investigations.
[Display omitted]
•Dimeric, trimeric, and tetrameric sesquiterpenoids are covered in the review.•Sesquiterpenoid oligomers are categorized by reaction types in biosynthetic pathways.•An attempt has been made to describe the mechanistic hypotheses in biosynthesis.•Natural sesquiterpenoid oligomers exhibit various bioactivities with potential. |
doi_str_mv | 10.1016/j.ejmech.2020.112622 |
format | article |
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[Display omitted]
•Dimeric, trimeric, and tetrameric sesquiterpenoids are covered in the review.•Sesquiterpenoid oligomers are categorized by reaction types in biosynthetic pathways.•An attempt has been made to describe the mechanistic hypotheses in biosynthesis.•Natural sesquiterpenoid oligomers exhibit various bioactivities with potential.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2020.112622</identifier><identifier>PMID: 32688203</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Bioactivities ; Biomimetic synthesis ; Biosynthetic pathways ; Drug Design ; Humans ; Polymerization ; Sesquiterpenes - chemistry ; Sesquiterpenes - pharmacology ; Sesquiterpenoid oligomers</subject><ispartof>European journal of medicinal chemistry, 2020-10, Vol.203, p.112622-112622, Article 112622</ispartof><rights>2020 Elsevier Masson SAS</rights><rights>Copyright © 2020 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-ac06d43696ea52b3f14796ad1f5ba6003b43650b7b9e840558bee6b4908f44c3</citedby><cites>FETCH-LOGICAL-c362t-ac06d43696ea52b3f14796ad1f5ba6003b43650b7b9e840558bee6b4908f44c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32688203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Wen-Yu</creatorcontrib><creatorcontrib>Yan, Juan-Juan</creatorcontrib><creatorcontrib>Liu, Tian-Tian</creatorcontrib><creatorcontrib>Gao, Jian</creatorcontrib><creatorcontrib>Huang, Hui-Lian</creatorcontrib><creatorcontrib>Sun, Cheng-Peng</creatorcontrib><creatorcontrib>Huo, Xiao-Kui</creatorcontrib><creatorcontrib>Deng, Sa</creatorcontrib><creatorcontrib>Zhang, Bao-Jing</creatorcontrib><creatorcontrib>Ma, Xiao-Chi</creatorcontrib><title>Natural sesquiterpenoid oligomers: A chemical perspective</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>Sesquiterpenoid oligomers, biogenetically assembled by at least two monomeric sesquiterpenoid units via diverse pathways, represent a unique class of natural products with distinct bioactivities. Herein, we provide a review covering the dimeric, trimeric, and tetrameric sesquiterpenoids categorized by reaction types in biosynthesis from a chemical perspective. Emphasis is focused on the biosynthetic oligomerization pathways of these interesting molecules and their related biological functions, which will supply inspiration for the total synthesis or biomimetic synthesis of more oligomeric sesquiterpenoids and further pharmacological investigations.
[Display omitted]
•Dimeric, trimeric, and tetrameric sesquiterpenoids are covered in the review.•Sesquiterpenoid oligomers are categorized by reaction types in biosynthetic pathways.•An attempt has been made to describe the mechanistic hypotheses in biosynthesis.•Natural sesquiterpenoid oligomers exhibit various bioactivities with potential.</description><subject>Animals</subject><subject>Bioactivities</subject><subject>Biomimetic synthesis</subject><subject>Biosynthetic pathways</subject><subject>Drug Design</subject><subject>Humans</subject><subject>Polymerization</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - pharmacology</subject><subject>Sesquiterpenoid oligomers</subject><issn>0223-5234</issn><issn>1768-3254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLw0AQgBdRbK3-A5EcvaTuO4kHoRRfUPTS-7K7mdgtSZPuJgX_vVtSPXoamPnm9SF0S_CcYCIftnPYNmA3c4ppTBEqKT1DU5LJPGVU8HM0xZSyVFDGJ-gqhC3GWEiML9GEUZnnFLMpKj50P3hdJwHCfnA9-A52rSuTtnZfbQM-PCaLxG6gcTZSXUx0YHt3gGt0Uek6wM0pztD65Xm9fEtXn6_vy8UqtUzSPtUWy5IzWUjQghpWEZ4VUpekEkbHa5iJRYFNZgrIORYiNwDS8ALnFeeWzdD9OLbz7X6A0KvGBQt1rXfQDkFRTkVeZIxkEeUjan0bgodKdd412n8rgtXRmdqq0Zk6OlOjs9h2d9owmAbKv6ZfSRF4GgGIbx4ceBWsg52F0vnoQpWt-3_DDxjCfes</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Zhao, Wen-Yu</creator><creator>Yan, Juan-Juan</creator><creator>Liu, Tian-Tian</creator><creator>Gao, Jian</creator><creator>Huang, Hui-Lian</creator><creator>Sun, Cheng-Peng</creator><creator>Huo, Xiao-Kui</creator><creator>Deng, Sa</creator><creator>Zhang, Bao-Jing</creator><creator>Ma, Xiao-Chi</creator><general>Elsevier Masson SAS</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></search><sort><creationdate>20201001</creationdate><title>Natural sesquiterpenoid oligomers: A chemical perspective</title><author>Zhao, Wen-Yu ; Yan, Juan-Juan ; Liu, Tian-Tian ; Gao, Jian ; Huang, Hui-Lian ; Sun, Cheng-Peng ; Huo, Xiao-Kui ; Deng, Sa ; Zhang, Bao-Jing ; Ma, Xiao-Chi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-ac06d43696ea52b3f14796ad1f5ba6003b43650b7b9e840558bee6b4908f44c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Bioactivities</topic><topic>Biomimetic synthesis</topic><topic>Biosynthetic pathways</topic><topic>Drug Design</topic><topic>Humans</topic><topic>Polymerization</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - pharmacology</topic><topic>Sesquiterpenoid oligomers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Wen-Yu</creatorcontrib><creatorcontrib>Yan, Juan-Juan</creatorcontrib><creatorcontrib>Liu, Tian-Tian</creatorcontrib><creatorcontrib>Gao, Jian</creatorcontrib><creatorcontrib>Huang, Hui-Lian</creatorcontrib><creatorcontrib>Sun, Cheng-Peng</creatorcontrib><creatorcontrib>Huo, Xiao-Kui</creatorcontrib><creatorcontrib>Deng, Sa</creatorcontrib><creatorcontrib>Zhang, Bao-Jing</creatorcontrib><creatorcontrib>Ma, Xiao-Chi</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><jtitle>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Wen-Yu</au><au>Yan, Juan-Juan</au><au>Liu, Tian-Tian</au><au>Gao, Jian</au><au>Huang, Hui-Lian</au><au>Sun, Cheng-Peng</au><au>Huo, Xiao-Kui</au><au>Deng, Sa</au><au>Zhang, Bao-Jing</au><au>Ma, Xiao-Chi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural sesquiterpenoid oligomers: A chemical perspective</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>203</volume><spage>112622</spage><epage>112622</epage><pages>112622-112622</pages><artnum>112622</artnum><issn>0223-5234</issn><eissn>1768-3254</eissn><abstract>Sesquiterpenoid oligomers, biogenetically assembled by at least two monomeric sesquiterpenoid units via diverse pathways, represent a unique class of natural products with distinct bioactivities. 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[Display omitted]
•Dimeric, trimeric, and tetrameric sesquiterpenoids are covered in the review.•Sesquiterpenoid oligomers are categorized by reaction types in biosynthetic pathways.•An attempt has been made to describe the mechanistic hypotheses in biosynthesis.•Natural sesquiterpenoid oligomers exhibit various bioactivities with potential.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>32688203</pmid><doi>10.1016/j.ejmech.2020.112622</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Bioactivities Biomimetic synthesis Biosynthetic pathways Drug Design Humans Polymerization Sesquiterpenes - chemistry Sesquiterpenes - pharmacology Sesquiterpenoid oligomers |
title | Natural sesquiterpenoid oligomers: A chemical perspective |
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