<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-19T02:47:30Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/13130" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/13130</identifier><datestamp>2026-10-18T20:56:45Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Isolation, characterization and antiproliferative activity of secondary metabolites from tanacetum alyssifolium (Bornm.) grierson</dc:title><dc:creator>Köksal, Ekrem</dc:creator><dc:creator>Ulutaş, Yakup</dc:creator><dc:creator>Şimşek, Samed</dc:creator><dc:creator>Bayraktar, Taha</dc:creator><dc:creator>Altay, Ahmet</dc:creator><dc:creator>Çatır, Mustafa</dc:creator><dc:creator>Demirtaş, İbrahim</dc:creator><dc:creator>Tüfekçi, Ali Rıza</dc:creator><dc:creator>Kandemir, Ali</dc:creator><dc:creator>Alp, Cemalettin</dc:creator><dc:creator>Anwer Alemdar, Mohammed B.</dc:creator><dc:creator>Akşit, Hüseyin</dc:creator><dc:subject>Cytotoxicity</dc:subject><dc:subject>MCF-7 cell line</dc:subject><dc:subject>Sesquiterpene lactones</dc:subject><dc:subject>Tanacetum alyssifolium</dc:subject><dc:subject>2,4 dihydroxy 6 methoxy acetophenone</dc:subject><dc:subject>acetophenone derivative</dc:subject><dc:subject>altissin</dc:subject><dc:subject>axillarin</dc:subject><dc:subject>coumarin derivative</dc:subject><dc:subject>doxorubicin</dc:subject><dc:subject>drug metabolite</dc:subject><dc:subject>flavonoid</dc:subject><dc:subject>fraxetin</dc:subject><dc:subject>fraxidin</dc:subject><dc:subject>isofraxidin</dc:subject><dc:subject>isofraxidin 7 glucoside</dc:subject><dc:subject>luteolin 7 glucoside</dc:subject><dc:subject>picein</dc:subject><dc:subject>rutoside</dc:subject><dc:subject>sesquiterpene lactone</dc:subject><dc:subject>tamirin</dc:subject><dc:subject>tanachin</dc:subject><dc:subject>tatridin A</dc:subject><dc:subject>unclassified drug</dc:subject><dc:subject>aerial plant part</dc:subject><dc:subject>antiproliferative activity</dc:subject><dc:subject>Article</dc:subject><dc:subject>controlled study</dc:subject><dc:subject>drug isolation</dc:subject><dc:subject>drug structure</dc:subject><dc:description>Secondary metabolites of Tanacetum alyssifolium (Bornm.) Grierson (Asteraceae) were investigated for the first time. Thirteen compounds including axillarin (1), Luteolin-7-O-β-glucoside (8) and rutin (13) as flavonoids, fraxetin (7), isofraxidin (9), isofraxidin-7-O-glucoside (11) and fraxidin (12) as coumarins, tatridin A (2), altissin (3), tamirin (4) and tanachin (5) as sesquiterpene lactones and 2,4-dihydroxy-6-methoxy acetophenone (6) and picein (10) as acetophenone derivatives were isolated from the methanol extract of the species. The structures of all isolated compounds were elucidated by 1D and 2D-NMR techniques and by comparing with the literature data. In addition, in vitro cytotoxic activity of all isolated compounds was evaluated against breast cancer MCF-7 cell line by XTT assay. Sesquiterpene lactones; tatridin A (2), tamirin (4) and tanachin (5) were found to be the most cytotoxic molecules against MCF-7 cell line. © 2020 ACG Publications.</dc:description><dc:publisher>ACG Publications</dc:publisher><dc:date>2021</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/13130</dc:identifier><dc:identifier>https://doi.org/10.25135/rnp.201.20.07.1702</dc:identifier><dc:identifier>1307-6167</dc:identifier><dc:language>en</dc:language><dc:relation>Records of Natural Products</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/13130</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>