New Diterpenes and Diterpene Glycosides with Antibacterial Activity from Soft Coral ILemnalia bournei/I
Five new biflorane-type diterpenoids, biofloranates E–I (1–5), and two new bicyclic diterpene glycosides, lemnaboursides H–I (6–7), along with the known lemnabourside, were isolated from the South China Sea soft coral Lemnalia bournei. Their chemical structures and stereochemistry were determined ba...
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creator | Han, Xiao Wang, Huiting Li, Bing Chen, Xiaoyi Li, Te Yan, Xia Ouyang, Han Lin, Wenhan He, Shan |
description | Five new biflorane-type diterpenoids, biofloranates E–I (1–5), and two new bicyclic diterpene glycosides, lemnaboursides H–I (6–7), along with the known lemnabourside, were isolated from the South China Sea soft coral Lemnalia bournei. Their chemical structures and stereochemistry were determined based on extensive spectroscopic methods, including time-dependent density functional theory (TDDFT) ECD calculations, as well as a comparison of them with the reported values. The antibacterial activities of the isolated compounds were evaluated against five pathogenic bacteria, and all of these diterpenes and diterpene glycosides showed antibacterial activities against Staphylococcus aureus and Bacillus subtilis, with MICs ranging from 4 to 64 µg/mL. In addition, these compounds did not exhibit noticeable cytotoxicities on A549, Hela, and HepG2 cancer cell lines, at 20 μM. |
doi_str_mv | 10.3390/md22040157 |
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Their chemical structures and stereochemistry were determined based on extensive spectroscopic methods, including time-dependent density functional theory (TDDFT) ECD calculations, as well as a comparison of them with the reported values. The antibacterial activities of the isolated compounds were evaluated against five pathogenic bacteria, and all of these diterpenes and diterpene glycosides showed antibacterial activities against Staphylococcus aureus and Bacillus subtilis, with MICs ranging from 4 to 64 µg/mL. In addition, these compounds did not exhibit noticeable cytotoxicities on A549, Hela, and HepG2 cancer cell lines, at 20 μM.</description><identifier>ISSN: 1660-3397</identifier><identifier>EISSN: 1660-3397</identifier><identifier>DOI: 10.3390/md22040157</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Antibacterial agents ; Chemical properties ; Diterpenes ; Glycosides ; Health aspects ; Identification and classification ; Pharmaceutical research ; Soft corals</subject><ispartof>Marine drugs, 2024-04, Vol.22 (4)</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27915,27916</link.rule.ids></links><search><creatorcontrib>Han, Xiao</creatorcontrib><creatorcontrib>Wang, Huiting</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Chen, Xiaoyi</creatorcontrib><creatorcontrib>Li, Te</creatorcontrib><creatorcontrib>Yan, Xia</creatorcontrib><creatorcontrib>Ouyang, Han</creatorcontrib><creatorcontrib>Lin, Wenhan</creatorcontrib><creatorcontrib>He, Shan</creatorcontrib><title>New Diterpenes and Diterpene Glycosides with Antibacterial Activity from Soft Coral ILemnalia bournei/I</title><title>Marine drugs</title><description>Five new biflorane-type diterpenoids, biofloranates E–I (1–5), and two new bicyclic diterpene glycosides, lemnaboursides H–I (6–7), along with the known lemnabourside, were isolated from the South China Sea soft coral Lemnalia bournei. Their chemical structures and stereochemistry were determined based on extensive spectroscopic methods, including time-dependent density functional theory (TDDFT) ECD calculations, as well as a comparison of them with the reported values. The antibacterial activities of the isolated compounds were evaluated against five pathogenic bacteria, and all of these diterpenes and diterpene glycosides showed antibacterial activities against Staphylococcus aureus and Bacillus subtilis, with MICs ranging from 4 to 64 µg/mL. In addition, these compounds did not exhibit noticeable cytotoxicities on A549, Hela, and HepG2 cancer cell lines, at 20 μM.</description><subject>Antibacterial agents</subject><subject>Chemical properties</subject><subject>Diterpenes</subject><subject>Glycosides</subject><subject>Health aspects</subject><subject>Identification and classification</subject><subject>Pharmaceutical research</subject><subject>Soft corals</subject><issn>1660-3397</issn><issn>1660-3397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptjM1OwzAQhC0EEiVw4QkscU7rjfPjHKMCJVIEB3qv1o5djBIbJYaqb48lkOgB7WF255tZQm6BLTmv2Wrss4zlDIrqjCygLFka7er8ZL8kV_P8zhgvRJ0vyP5ZH-i9DXr60E7PFF3_d9LNcFR-tn0EBxveaOOClagitjjQRgX7ZcORmsmP9NWbQNd-iqDt9OhwsEil_5yctqv2mlwYHGZ986sJ2T4-bNdPafeyaddNl-7Lqk45qhKMFFIWBgE45L0AIUxkdSUYlGh6linIjZSgEQRkTOeFVgZRZlnFE3L383aPg95ZZ3yYUI12VrumqnlRcBYlIct_UnF6PVrlnTY2-ieFb0HlZ9U</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Han, Xiao</creator><creator>Wang, Huiting</creator><creator>Li, Bing</creator><creator>Chen, Xiaoyi</creator><creator>Li, Te</creator><creator>Yan, Xia</creator><creator>Ouyang, Han</creator><creator>Lin, Wenhan</creator><creator>He, Shan</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20240401</creationdate><title>New Diterpenes and Diterpene Glycosides with Antibacterial Activity from Soft Coral ILemnalia bournei/I</title><author>Han, Xiao ; Wang, Huiting ; Li, Bing ; Chen, Xiaoyi ; Li, Te ; Yan, Xia ; Ouyang, Han ; Lin, Wenhan ; He, Shan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g679-3ac61fb8bb5fa11314d8188f679978016afd02c14fbb1ea18120e45ecfaab2273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibacterial agents</topic><topic>Chemical properties</topic><topic>Diterpenes</topic><topic>Glycosides</topic><topic>Health aspects</topic><topic>Identification and classification</topic><topic>Pharmaceutical research</topic><topic>Soft corals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Xiao</creatorcontrib><creatorcontrib>Wang, Huiting</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Chen, Xiaoyi</creatorcontrib><creatorcontrib>Li, Te</creatorcontrib><creatorcontrib>Yan, Xia</creatorcontrib><creatorcontrib>Ouyang, Han</creatorcontrib><creatorcontrib>Lin, Wenhan</creatorcontrib><creatorcontrib>He, Shan</creatorcontrib><jtitle>Marine drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Xiao</au><au>Wang, Huiting</au><au>Li, Bing</au><au>Chen, Xiaoyi</au><au>Li, Te</au><au>Yan, Xia</au><au>Ouyang, Han</au><au>Lin, Wenhan</au><au>He, Shan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Diterpenes and Diterpene Glycosides with Antibacterial Activity from Soft Coral ILemnalia bournei/I</atitle><jtitle>Marine drugs</jtitle><date>2024-04-01</date><risdate>2024</risdate><volume>22</volume><issue>4</issue><issn>1660-3397</issn><eissn>1660-3397</eissn><abstract>Five new biflorane-type diterpenoids, biofloranates E–I (1–5), and two new bicyclic diterpene glycosides, lemnaboursides H–I (6–7), along with the known lemnabourside, were isolated from the South China Sea soft coral Lemnalia bournei. Their chemical structures and stereochemistry were determined based on extensive spectroscopic methods, including time-dependent density functional theory (TDDFT) ECD calculations, as well as a comparison of them with the reported values. The antibacterial activities of the isolated compounds were evaluated against five pathogenic bacteria, and all of these diterpenes and diterpene glycosides showed antibacterial activities against Staphylococcus aureus and Bacillus subtilis, with MICs ranging from 4 to 64 µg/mL. In addition, these compounds did not exhibit noticeable cytotoxicities on A549, Hela, and HepG2 cancer cell lines, at 20 μM.</abstract><pub>MDPI AG</pub><doi>10.3390/md22040157</doi></addata></record> |
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subjects | Antibacterial agents Chemical properties Diterpenes Glycosides Health aspects Identification and classification Pharmaceutical research Soft corals |
title | New Diterpenes and Diterpene Glycosides with Antibacterial Activity from Soft Coral ILemnalia bournei/I |
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