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This study identifies quinoxaline derivatives as novel inhibitors of the LRP5/6-sclerostin interaction, which is crucial for regulating the Wnt/b-catenin signaling pathway and has implications for osteoporosis treatment. Through pharmacophore-based virtual screening and docking simulations, the compound BMD4503 was optimized to enhance its binding affinity and disrupt sclerostin

Author
900chp
Language
EN

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