Journal of Agricultural and Food Chemistry · 2022 · 10 citations · 43 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsAntiviral AgentsAntiviral PharmacologyLigand-based DesignMolecular SimilarityQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisAntiviral Agent SelectionAntiviral Drug DesignAntiviral Mechanisms Of ActionAntiviral Structure-activity RelationshipsComputational Structure-activity ModelingDefense Response MechanismsStructure - Activity Relationship OptimizationStructure-activity Relationship Modeling
A series of cytosine derivatives containing a sulfonamide moiety were designed and synthesized, and their antiviral activities against pepper mild mottle virus (PMMoV) were systematically evaluated. Then, a three-dimensional quantitative structure-activity relationship (3D-QSAR) model was constructed to study the structure-activity relationship according to the pEC50 of the compounds’ protective activities. Next, compound A32 with preferable antiviral activity on PMMoV was obtained based on the CoMSIA and CoMFA models, with an EC50 of 19.5 μg/mL, which was superior to the template molecule A25 (21.3 μg/mL) and ningnanmycin (214.0 μg/mL). In addition, further studies showed that the antiviral activity of compound A32 against PMMoV was in accord with the up-regulation of proteins expressed in the defense response and carbon fixation in photosynthetic organisms. These results indicated that cytosine derivatives containing a sulfonamide moiety could be used as novel potential antiviral agents for further research and development.
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Nicola Chirico, Paola Gramatica · Journal of Chemical Information and Modeling · 2011 · 752 citations · Full text
Virus Diseases of Peppers (Capsicum spp.) and Their Control
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Synthesis and Antiviral Activity of 5‑(4‑Chlorophenyl)-1,3,4-Thiadiazole Sulfonamides
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