<?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>2026-10-19T01:06:14Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11901" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/11901</identifier><datestamp>2026-10-18T21:13:18Z</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>Two new compounds from endemic Centaurea paphlagonica (Bornm.) Wagenitz and their cytotoxic activities</dc:title><dc:creator>Tüfekçi, Ali Rıza</dc:creator><dc:creator>Demirtaş, İbrahim</dc:creator><dc:creator>Akşit, Hüseyin</dc:creator><dc:creator>Arslan, Şevki</dc:creator><dc:creator>Kocabıyık, Kübra</dc:creator><dc:creator>Zeybek, Sibel</dc:creator><dc:creator>Ozen, Tevfik</dc:creator><dc:creator>Köksal, Ekrem</dc:creator><dc:subject>antiproliferative activity</dc:subject><dc:subject>Asteraceae</dc:subject><dc:subject>Centaurea paphlagonica</dc:subject><dc:subject>isolation</dc:subject><dc:subject>MTT</dc:subject><dc:subject>Antineoplastic Agents</dc:subject><dc:subject>Caco-2 Cells</dc:subject><dc:subject>Centaurea</dc:subject><dc:subject>Chlorogenic Acid</dc:subject><dc:subject>HEK293 Cells</dc:subject><dc:subject>Humans</dc:subject><dc:subject>Methyl Ethers</dc:subject><dc:subject>Plant Extracts</dc:subject><dc:subject>3 o feruloylquinic acid</dc:subject><dc:subject>3,4 dihydroxy benzoic acid</dc:subject><dc:subject>5 o caffeoylshikimic acid</dc:subject><dc:subject>8alpha o (2',3' dihydroxyisobutyryl)desacylcynaropicrin</dc:subject><dc:subject>alkaloid</dc:subject><dc:subject>catechol</dc:subject><dc:subject>Centaurea paphlagonica extract</dc:subject><dc:subject>chlorogenic acid methyl ester</dc:subject><dc:subject>cirsiliol</dc:subject><dc:subject>cynarine</dc:subject><dc:subject>desacylcynaropicrin</dc:subject><dc:subject>diosmetin 6 c beta glucopyranoside</dc:subject><dc:subject>flavonoid</dc:subject><dc:subject>flavonoid glycoside</dc:subject><dc:subject>glycoside</dc:subject><dc:subject>herbaceous agent</dc:subject><dc:subject>isoorientin</dc:subject><dc:description>Centaurea paphlagonica (Bornm.) Wagenitz is an endemic plant in Turkey. Pyrocatechol, vanillic acid, 3,4-dihydroxy benzoic acid, 5-O-caffeoylshikimic acid, tamarixetin, chlorogenic acid methyl ester, quercetin, 1,3-dicaffeoylquinic acid, tamarixetin-7-O-β-D-glucopyranoside, quercimetrin, daucosterin, paphlagonicanin B, tamarixetin-7-O-β-rutinoside, rutin, chlorogenic acid, isoorientin, orientin, 3-O-feruloylquinic acid, quercetagetin-3-methyl ether 6-O-β-glucopyranoside, diosmetin 6-C-β-glucopyranoside, quercetagetin 4′-methyl ether 7-O-β-glucopyranoside, paphlagonicanin A, nepetin, cirsiliol, desacylcynaropicrin, and 8α-O-(2′,3′-dihydroxyisobutyryl) desacylcynaropicrin were isolated from both flower and aerial parts of C. paphlagonica. These compounds were identified using 1D and 2D NMR methods and ESI-MS. The MTT assay assessed the antiproliferative activities of all isolated (known and new compounds) compounds on Caco-2, LNCaP, A549, HeLa, and HEK-293 cell lines. The 8α-O-(2′,3′-dihydroxyisobutyryl) desacylcynaropicrin demonstrated the highest activity against CaCo-2 and HeLa cancer cell lines. © 2023 John Wiley &amp; Sons Ltd.</dc:description><dc:publisher>John Wiley and Sons Inc</dc:publisher><dc:date>2024</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/11901</dc:identifier><dc:identifier>https://doi.org/10.1111/cbdd.14409</dc:identifier><dc:identifier>1747-0277</dc:identifier><dc:language>en</dc:language><dc:relation>Chemical Biology and Drug Design</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/11901</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>