<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bensaad, Mohamed Sabri</style></author><author><style face="normal" font="default" size="100%">Allaoua, Zina</style></author><author><style face="normal" font="default" size="100%">Kahoul, Mohamed Amine</style></author><author><style face="normal" font="default" size="100%">Diana C. G. A. Pinto</style></author><author><style face="normal" font="default" size="100%">Chawki Bensouici</style></author><author><style face="normal" font="default" size="100%">Salah Akkal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">GC-Ms, UHPLC&amp;ndash;MS/MSn Phytoconstituents Characterization and Physio-pharmacological Investigation of Silene colorata subsp. amphorina (Pomel) Batt. From Northeastern Algeria</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry &amp; Biodiversity</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2026</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/10.1002/cbdv.71578</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">23</style></volume><pages><style face="normal" font="default" size="100%">e71578</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Natural remedies combined with bioinformatics accelerate the formulation of safer, targeted drugs. This study provides a comprehensive description of the phytochemical and pharmacological aspects of Silene colorata. Binding profiles of eight identified compounds were simulated against α-amylase. GC-MS analysis revealed 57 compounds, mainly fatty acids and esters (73.65%), while UHPLC–MS/MS identified 2′,4′-dihydroxychalcone (20.72%), (epi)gallocatechin-C-hexoside (12.53%), apigetrin (10.10%), and hexahydroxyheptanoic acid (8.57%) as major components. The hydro-alcoholic extract showed a strong antiradical effect (IC50 = 7.57 ± 0.26 µg/mL by ABTS assay; A0.50 = 48.93 ± 3.88 µg/mL by phenanthroline assay). Its sun protection factor (SPF) was also the highest (40.561 ± 0.87). The chloroform fraction showed notable activity against α-amylase (IC50 = 22.86 ± 3.19 µg/mL) and butyrylcholinesterase (IC50 = 111.08 ± 4.72 µg/mL). The complex 3-tetradecyn-1-ol and α-amylase appeared more stable, but in an antagonistic manner (−4.8 kcal/mol). While this work reveals crucial findings, further in vivo studies are needed to confirm and expand on these results.</style></abstract><issue><style face="normal" font="default" size="100%">8</style></issue></record></records></xml>