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Medicinal Chemistry (Shariqah (United Arab Emirates))|November 10, 2018
Synthesis, Anti-Varicella-Zoster Virus and Anti-Cytomegalovirus Activity of 4,5-Disubstituted 1,2,3-(1H)-TriazolesWei-Yuan Yuan, Xue Chen, Ning-Ning Liu, et al.Biological & Pharmaceutical Bulletin|April 5, 2016
Design, Synthesis, and Molecular Docking Studies of a Conjugated Thiadiazole-Thiourea Scaffold as Antituberculosis AgentsEsra Tatar, Sevgi Karakuş, Şükriye Güniz Küçükgüzel, et al.Antiviral Research|January 27, 2019
Antiviral activity spectrum of phenoxazine nucleoside derivativesLiubov I Kozlovskaya, Graciela Andrei, Alexey A Orlov, et al.Antiviral Research|June 29, 2024
CRISPR/Cas9-mediated genome editing of the thymidine kinase gene in a clinical HSV-1 isolate identifies F289S as novel acyclovir-resistant mutationShuxuan Zheng, Georges M G M Verjans, Anouk Evers, et al.Journal of Medicinal Chemistry|September 3, 2010
Synthesis of ester prodrugs of 9-(S)-[3-hydroxy-2-(phosphonomethoxy)propyl]-2,6-diaminopurine (HPMPDAP) as anti-poxvirus agentsMarcela Krecmerová, Antoín Holý, Graciela Andrei, et al.Ebiomedicine|November 30, 2024
A retrospective genomic characterisation of the 2022 mpox outbreak in Belgium, and in vitro assessment of three antiviral compoundsTony Wawina-Bokalanga, Bert Vanmechelen, Anne-Sophie Logist, et al.Molecular Diversity|June 30, 2026
Discovery of novel perillyl and myrtenyl nucleobase conjugates as dual anti-Alzheimer and antimicrobial agentsSaida Lachhab, Soukaina Elmoussaoui, Meriem Rafya, et al.European Journal of Medicinal Chemistry|November 4, 2022
Rational design of the zonulin inhibitor AT1001 derivatives as potential anti SARS-CoV-2Simone Di Micco, Rahila Rahimova, Marina Sala, et al.The Journal of Antimicrobial Chemotherapy|October 25, 2007
Preclinical development of bicyclic nucleoside analogues as potent and selective inhibitors of varicella zoster virusChristopher McGuigan, Ranjith N Pathirana, Marco Migliore, et al.Journal of Medicinal Chemistry|December 7, 2010
Novel antiviral C5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substratesDimitri Topalis, Ugo Pradère, Vincent Roy, et al.Pageof 26