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Xiao-Li Xu

Researcher at China Pharmaceutical University

Publications -  84
Citations -  1563

Xiao-Li Xu is an academic researcher from China Pharmaceutical University. The author has contributed to research in topics: Virtual screening & Docking (molecular). The author has an hindex of 21, co-authored 78 publications receiving 1138 citations.

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Discovery of potent Keap1-Nrf2 protein-protein interaction inhibitor based on molecular binding determinants analysis.

TL;DR: This work successfully designed and characterized the most potent protein-protein interaction (PPI) inhibitor of Keap1-Nrf2, compound 2, with K(D) value of 3.59 nM binding to Keap 1 for the first time to single-digit nanomolar.
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NRF2 promotes breast cancer cell proliferation and metastasis by increasing RhoA/ROCK pathway signal transduction.

TL;DR: Findings indicate that NRF2 silencing-mediated reduction of RhoA expression contributes, at least in part, to the poor outcome of breast cancer patients with highNRF2 expression.
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Heat Shock Protein 90 Inhibitors: An Update on Achievements, Challenges, and Future Directions.

TL;DR: This review summarizes the recent progress in Hsp90 inhibitors and suggests novel HSp90 inhibitory strategies that are expected to breakthrough with satisfactory efficacy and safety profiles.
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Structure-Activity and Structure-Property Relationship and Exploratory in Vivo Evaluation of the Nanomolar Keap1-Nrf2 Protein-Protein Interaction Inhibitor

TL;DR: Compound 18e could reduce the level of circulating pro-inflammatory cytokines induced by LPS and relieve the inflammatory response, and a preliminary investigation of the structure-activity and structure-property relationships of the ring systems to improve the drug-like properties was conducted.
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Targeting Stimulator of Interferon Genes (STING): A Medicinal Chemistry Perspective

TL;DR: The current understanding of STING structure is summarized, the status quo of STings modulators is surveyed, established bioassay methods are compared, the chemical structures and bioactivities of agonists and inhibitors are reviewed, and suggestions and insights for the future exploitation of STing modulators are proposed.