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New Sesquiterpene Glycosides from the Flowers of IAster koraiensis/I and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation
In total, four new eudesmane-type sesquiterpene glycosides, askoseosides A–D (1–4), and 18 known compounds (5–22) were isolated from the flowers of Aster koraiensis via chromatographic techniques. Chemical structures of the isolated compounds were identified by spectroscopic/spectrometric methods, i...
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Published in: | Plants 2023, Vol.12 (8) |
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creator | Seo, Young-Hye Kim, Ji-Young Ryu, Seung-Mok Hwang, Sun-Young Lee, Mee-Hyun Kim, Nahyun Son, Hojun Lee, A-Yeong Kim, Hyo-Seon Moon, Byeong-Cheol Jang, Dae-Sik Lee, Jun |
description | In total, four new eudesmane-type sesquiterpene glycosides, askoseosides A–D (1–4), and 18 known compounds (5–22) were isolated from the flowers of Aster koraiensis via chromatographic techniques. Chemical structures of the isolated compounds were identified by spectroscopic/spectrometric methods, including NMR and HRESIMS, and the absolute configuration of the new compounds (1 and 2) was performed by electronic circular dichroism (ECD) studies. Further, the anticancer activities of the isolated compounds (1–22) were evaluated using the epidermal growth factor (EGF)-induced as well as the 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced cell transformation assay. Among the 22 compounds, compounds 4, 9, 11, 13–15, 17, 18, and 22 significantly inhibited both EGF- and TPA-induced colony growth. In particular, askoseoside D (4, EGF: 57.8%; TPA: 67.1%), apigenin (9, EGF: 88.6%; TPA: 80.2%), apigenin-7-O-β-d-glucuronopyranoside (14, EGF: 79.2%; TPA: 70.7%), and 1-(3′,4′-dihydroxycinnamoyl) cyclopentane-2,3-diol (22, EGF: 60.0%; TPA: 72.1%) showed higher potent activities. |
doi_str_mv | 10.3390/plants12081726 |
format | report |
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Chemical structures of the isolated compounds were identified by spectroscopic/spectrometric methods, including NMR and HRESIMS, and the absolute configuration of the new compounds (1 and 2) was performed by electronic circular dichroism (ECD) studies. Further, the anticancer activities of the isolated compounds (1–22) were evaluated using the epidermal growth factor (EGF)-induced as well as the 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced cell transformation assay. Among the 22 compounds, compounds 4, 9, 11, 13–15, 17, 18, and 22 significantly inhibited both EGF- and TPA-induced colony growth. In particular, askoseoside D (4, EGF: 57.8%; TPA: 67.1%), apigenin (9, EGF: 88.6%; TPA: 80.2%), apigenin-7-O-β-d-glucuronopyranoside (14, EGF: 79.2%; TPA: 70.7%), and 1-(3′,4′-dihydroxycinnamoyl) cyclopentane-2,3-diol (22, EGF: 60.0%; TPA: 72.1%) showed higher potent activities.</description><identifier>ISSN: 2223-7747</identifier><identifier>EISSN: 2223-7747</identifier><identifier>DOI: 10.3390/plants12081726</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Botanical research ; Chromatography ; Compositae ; Epidermal growth factor ; Genetic aspects ; Physiological aspects ; Sesquiterpenes ; Spectra ; Structure</subject><ispartof>Plants, 2023, Vol.12 (8)</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Seo, Young-Hye</creatorcontrib><creatorcontrib>Kim, Ji-Young</creatorcontrib><creatorcontrib>Ryu, Seung-Mok</creatorcontrib><creatorcontrib>Hwang, Sun-Young</creatorcontrib><creatorcontrib>Lee, Mee-Hyun</creatorcontrib><creatorcontrib>Kim, Nahyun</creatorcontrib><creatorcontrib>Son, Hojun</creatorcontrib><creatorcontrib>Lee, A-Yeong</creatorcontrib><creatorcontrib>Kim, Hyo-Seon</creatorcontrib><creatorcontrib>Moon, Byeong-Cheol</creatorcontrib><creatorcontrib>Jang, Dae-Sik</creatorcontrib><creatorcontrib>Lee, Jun</creatorcontrib><title>New Sesquiterpene Glycosides from the Flowers of IAster koraiensis/I and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation</title><title>Plants</title><description>In total, four new eudesmane-type sesquiterpene glycosides, askoseosides A–D (1–4), and 18 known compounds (5–22) were isolated from the flowers of Aster koraiensis via chromatographic techniques. Chemical structures of the isolated compounds were identified by spectroscopic/spectrometric methods, including NMR and HRESIMS, and the absolute configuration of the new compounds (1 and 2) was performed by electronic circular dichroism (ECD) studies. Further, the anticancer activities of the isolated compounds (1–22) were evaluated using the epidermal growth factor (EGF)-induced as well as the 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced cell transformation assay. Among the 22 compounds, compounds 4, 9, 11, 13–15, 17, 18, and 22 significantly inhibited both EGF- and TPA-induced colony growth. In particular, askoseoside D (4, EGF: 57.8%; TPA: 67.1%), apigenin (9, EGF: 88.6%; TPA: 80.2%), apigenin-7-O-β-d-glucuronopyranoside (14, EGF: 79.2%; TPA: 70.7%), and 1-(3′,4′-dihydroxycinnamoyl) cyclopentane-2,3-diol (22, EGF: 60.0%; TPA: 72.1%) showed higher potent activities.</description><subject>Botanical research</subject><subject>Chromatography</subject><subject>Compositae</subject><subject>Epidermal growth factor</subject><subject>Genetic aspects</subject><subject>Physiological aspects</subject><subject>Sesquiterpenes</subject><subject>Spectra</subject><subject>Structure</subject><issn>2223-7747</issn><issn>2223-7747</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2023</creationdate><recordtype>report</recordtype><sourceid/><recordid>eNqVT8FOwzAMjRBITLArZ_9AtzYdbXespnX0MiHROwqtQw1pMuKMib_gkwmCA1dsS35-eu9JFuImSxd5vk6XB6Ns4EymVVbK4kzMpJR5Upar8vwPvhRz5pc0VhUnK2bic48neEB-O1JAf0CLsDMfvWMakEF7N0EYERrjTugZnIa25qiEV-cVoWXiZQvKDtCNSB5aO9ITBXIW6j7Qe4QxJ17bXZP86O7rpLXDsccBNmgMdF5Z1s5P6tt2LS60Mozz330lFs2229wlz8rgI1ntgld97AEn6p1FTZGv43OrYl3dyvzfhi9raGWH</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Seo, Young-Hye</creator><creator>Kim, Ji-Young</creator><creator>Ryu, Seung-Mok</creator><creator>Hwang, Sun-Young</creator><creator>Lee, Mee-Hyun</creator><creator>Kim, Nahyun</creator><creator>Son, Hojun</creator><creator>Lee, A-Yeong</creator><creator>Kim, Hyo-Seon</creator><creator>Moon, Byeong-Cheol</creator><creator>Jang, Dae-Sik</creator><creator>Lee, Jun</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20230401</creationdate><title>New Sesquiterpene Glycosides from the Flowers of IAster koraiensis/I and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation</title><author>Seo, Young-Hye ; Kim, Ji-Young ; Ryu, Seung-Mok ; Hwang, Sun-Young ; Lee, Mee-Hyun ; Kim, Nahyun ; Son, Hojun ; Lee, A-Yeong ; Kim, Hyo-Seon ; Moon, Byeong-Cheol ; Jang, Dae-Sik ; Lee, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_infotracacademiconefile_A7474698523</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Botanical research</topic><topic>Chromatography</topic><topic>Compositae</topic><topic>Epidermal growth factor</topic><topic>Genetic aspects</topic><topic>Physiological aspects</topic><topic>Sesquiterpenes</topic><topic>Spectra</topic><topic>Structure</topic><toplevel>online_resources</toplevel><creatorcontrib>Seo, Young-Hye</creatorcontrib><creatorcontrib>Kim, Ji-Young</creatorcontrib><creatorcontrib>Ryu, Seung-Mok</creatorcontrib><creatorcontrib>Hwang, Sun-Young</creatorcontrib><creatorcontrib>Lee, Mee-Hyun</creatorcontrib><creatorcontrib>Kim, Nahyun</creatorcontrib><creatorcontrib>Son, Hojun</creatorcontrib><creatorcontrib>Lee, A-Yeong</creatorcontrib><creatorcontrib>Kim, Hyo-Seon</creatorcontrib><creatorcontrib>Moon, Byeong-Cheol</creatorcontrib><creatorcontrib>Jang, Dae-Sik</creatorcontrib><creatorcontrib>Lee, Jun</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seo, Young-Hye</au><au>Kim, Ji-Young</au><au>Ryu, Seung-Mok</au><au>Hwang, Sun-Young</au><au>Lee, Mee-Hyun</au><au>Kim, Nahyun</au><au>Son, Hojun</au><au>Lee, A-Yeong</au><au>Kim, Hyo-Seon</au><au>Moon, Byeong-Cheol</au><au>Jang, Dae-Sik</au><au>Lee, Jun</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>New Sesquiterpene Glycosides from the Flowers of IAster koraiensis/I and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation</atitle><jtitle>Plants</jtitle><date>2023-04-01</date><risdate>2023</risdate><volume>12</volume><issue>8</issue><issn>2223-7747</issn><eissn>2223-7747</eissn><abstract>In total, four new eudesmane-type sesquiterpene glycosides, askoseosides A–D (1–4), and 18 known compounds (5–22) were isolated from the flowers of Aster koraiensis via chromatographic techniques. Chemical structures of the isolated compounds were identified by spectroscopic/spectrometric methods, including NMR and HRESIMS, and the absolute configuration of the new compounds (1 and 2) was performed by electronic circular dichroism (ECD) studies. Further, the anticancer activities of the isolated compounds (1–22) were evaluated using the epidermal growth factor (EGF)-induced as well as the 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced cell transformation assay. Among the 22 compounds, compounds 4, 9, 11, 13–15, 17, 18, and 22 significantly inhibited both EGF- and TPA-induced colony growth. In particular, askoseoside D (4, EGF: 57.8%; TPA: 67.1%), apigenin (9, EGF: 88.6%; TPA: 80.2%), apigenin-7-O-β-d-glucuronopyranoside (14, EGF: 79.2%; TPA: 70.7%), and 1-(3′,4′-dihydroxycinnamoyl) cyclopentane-2,3-diol (22, EGF: 60.0%; TPA: 72.1%) showed higher potent activities.</abstract><pub>MDPI AG</pub><doi>10.3390/plants12081726</doi></addata></record> |
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subjects | Botanical research Chromatography Compositae Epidermal growth factor Genetic aspects Physiological aspects Sesquiterpenes Spectra Structure |
title | New Sesquiterpene Glycosides from the Flowers of IAster koraiensis/I and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation |
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