ArticleJournal of advanced research2026
Computational discovery and repurposing of chloramphenicol succinate as a potent P2Y
Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
10 authors.
Funding
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Abstract
introductionThe P2Y
objectivesThis study aimed to computationally identify FDA-approved or experimental drugs as novel P2Y
methodsA multi-step computational pipeline integrated structure-based virtual screening (SBVS) of DrugBank drug compounds, molecular docking (Glide XP/AutoDock Vina), molecular dynamics (MD) simulations, and MM/GBSA binding free energy calculations. Top candidates underwent in vitro P2Y
resultsChloramphenicol succinate (DB07565), an antibiotic, emerged as a potent P2Y
conclusionThis study demonstrates that computational repurposing successfully identifies DB07565 as a high-affinity P2Y
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Registered trials
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