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Frontiers in Microbiology|October 24, 2022
Development and validation of a sensitive LC-MS/MS method for determination of intracellular concentration of fluconazole in Candida albicansXiaofei Wang, Xiaojuan Wang, Tongkai Cai, et al.Bioorganic & Medicinal Chemistry Letters|September 15, 2009
Discovery of highly potent novel antifungal azoles by structure-based rational designWenya Wang, Chunquan Sheng, Xiaoying Che, et al.European Journal of Medicinal Chemistry|March 18, 2011
Design and synthesis of antifungal benzoheterocyclic derivatives by scaffold hoppingChunquan Sheng, Xiaoying Che, Wenya Wang, et al.Chemical Biology & Drug Design|May 19, 2011
Structure-based design, synthesis, and antifungal activity of new triazole derivativesChunquan Sheng, Xiaoying Che, Wenya Wang, et al.European Journal of Medicinal Chemistry|October 11, 2011
Design and synthesis of novel triazole antifungal derivatives by structure-based bioisosterismChunquan Sheng, Xiaoying Che, Wenya Wang, et al.Bioorganic & Medicinal Chemistry Letters|December 31, 2010
New azoles with antifungal activity: Design, synthesis, and molecular dockingXiaoyun Chai, Jun Zhang, Yongbing Cao, et al.Yeast (Chichester, England)|December 25, 2009
Candida albicans CaPTC6 is a functional homologue for Saccharomyces cerevisiae ScPTC6 and encodes a type 2C protein phosphataseLiquan Yu, Jingwen Zhao, Jinrong Feng, et al.European Journal of Medicinal Chemistry|May 3, 2011
Design, synthesis and molecular docking studies of novel triazole as antifungal agentXiaoyun Chai, Jun Zhang, Yongbing Cao, et al.Journal of Medicinal Chemistry|February 26, 2014
Design, synthesis, and structure-activity relationship studies of novel fused heterocycles-linked triazoles with good activity and water solubilityXufeng Cao, Zhaoshuan Sun, Yongbing Cao, et al.Ageing Research Reviews|July 2, 2026
Macrophage Senescence and Programmed Cell Death in Atherosclerosis: Mechanisms, Cross-Talk, and Emerging Therapeutic StrategiesChenqin Xu, Chuang Ke, Yi-Lang Zhong, et al.Pageof 8