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dc.contributor.authorObadawo, Babatunde Samuelvi
dc.contributor.otherAsogwa, Uchennavi
dc.contributor.otherAli, Abdualbaset Ahmedvi
dc.date.accessioned2023-03-28T04:03:05Z-
dc.date.available2023-03-28T04:03:05Z-
dc.date.issued2022-
dc.identifier.issn2522-8307vi
dc.identifier.urihttp://tailieuso.tlu.edu.vn/handle/DHTL/12625-
dc.description.abstractCoxsackievirus group B (CVBs) are common enteroviruses associated with several diseases from etiologically to inflammatory cardiomyopathies and constitute a severe cause of mortality in newborn resulting in severe meningitis, fulminant infection, myocarditis, and encephalitis. While Berberian (BBR) is an effective antivirus and possesses potentials of suppressing CVB replication, Zeng et al. explored a structural modification of BBR by incorporating a substituted primary amine enhance antiviral potency and safety. Based on data set from Zeng et al., we attempted to propose a QSAR model that can predict the bioactivity of unknown compounds as anti-CVB1.vi
dc.description.urihttps://link.springer.com/article/10.1186/s42269-022-00698-zvi
dc.languageen_USvi
dc.relation.ispartofseriesBulletin of the National Research Centre, Volume 46 (2022), Article number: 14vi
dc.subjectBerberian (BBR)vi
dc.subjectCoxsackievirus B (CVBs)vi
dc.subjectQSARvi
dc.titleQSAR studies of BBR analogues against coxsackievirus B1vi
dc.typeBBvi
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