<?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>2026-10-19T00:02:53Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10235" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10235</identifier><datestamp>2026-10-18T20:43:03Z</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>Analytical profiling of vescalagin: Antioxidant Capacity and multi-enzyme inhibition spectrum</dc:title><dc:creator>Gulcin, İlhami</dc:creator><dc:creator>Durmaz, Lokman</dc:creator><dc:creator>Karagecili, Hasan</dc:creator><dc:creator>Ozden, Eda Mehtap</dc:creator><dc:creator>Erturk, Adem</dc:creator><dc:creator>Bingol, Zeynebe</dc:creator><dc:subject>Acetylcholinesterase</dc:subject><dc:subject>Antioxidant activity</dc:subject><dc:subject>Butyrylcholinesterase</dc:subject><dc:subject>Carbonic anhydrase</dc:subject><dc:subject>Polyphenolic compound</dc:subject><dc:subject>Vescalagin</dc:subject><dc:subject>α-glycosidase</dc:subject><dc:description>Vescalagin have been isolated from Camu-camu (Myrciaria dubia). Vescalagin compound was a found to be the main C-glycosidic ellagitannin with a bridging open ring d -glucose. A variety of techniques were used to assess vescalagin's antioxidant capacity, including its capacity to reduce potassium ferric cyanide, scavenge N,N-dimethyl-p-phenylenediamine dihydrochloride radicals (DMPD•+), scavenge 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radicals (ABTS•+), scavenge 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH·), and reduce cupric ions (Cu2+). Likewise, butylated hydroxyanisole (BHA), Trolox, α-tocopherol, and butylated hydroxytoluene (BHT) were employed as reference antioxidants for assessment. For DPPH radical scavenging, vescalagin had an IC50 value of 9.65 μg/mL (r2: 0.9225), while the IC50 values for BHA, BHT, α-Tocopherol, and Trolox were 10.10, 25.95, 11.31, and 7.05 μg/mL properly. The resarch revealed that vescalagin reacted better than BHA, α-tocopherol, and BHT with regard to DPPH· scavenging, but nearly similiar to Trolox. Vescalagin was also shown to be a polyphenolic secondary metabolite that inhibited a number of metabolic enzymes, particularly α-glycosidase, carbonic anhydrases I and II (CA I and II), butyrylcholinesterase (BChE), and acetylcholinesterase (AChE). The Ki values of vescalagin showed 5.87, 3.89, 11.75, 16.23, and 16.08 nM towards AChE, BChE, hCA I, hCA II, and α-glycosidase, respectively. These enzymes are linked to several ilness such as diabetes, Alzheimer disease (AD), epilepsy and glaucoma. The obtained findings clearly indicate that vescalagin can be used as a reference polyphenolic antioxidant or enzyme inhibitor in analytical and screening assays. © 2026 The Author(s).</dc:description><dc:publisher>Elsevier B.V.</dc:publisher><dc:date>2026</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/10235</dc:identifier><dc:identifier>https://doi.org/10.1016/j.talo.2026.100624</dc:identifier><dc:identifier>2666-8319</dc:identifier><dc:language>en</dc:language><dc:relation>Talanta Open</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/10235</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>