Changlun Shao

Ocean University of China 
"Changlun Shao"
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Guo FW, Zhang Q, Gu YC, et al. (2023) Sulfur-containing marine natural products as leads for drug discovery and development. Current Opinion in Chemical Biology. 75: 102330
Qu Y, Zhou TY, Guo FW, et al. (2023) Analogues of natural products yaequinolones as potential inflammatory inhibitors: Design, synthesis and biological evaluation. European Journal of Medicinal Chemistry. 250: 115183
Han YQ, Zhang Q, Xu WF, et al. (2023) Targeted isolation of antitubercular cycloheptapeptides and an unusual pyrroloindoline-containing new analog, asperpyrroindotide A, using LC-MS/MS-based molecular networking. Marine Life Science & Technology. 1-9
Guo FW, Mou XF, Qu Y, et al. (2022) Scalable total synthesis of (+)-aniduquinolone A and its acid-catalyzed rearrangement to aflaquinolones. Communications Chemistry. 5: 35
Xu L, Guo FW, Zhang XQ, et al. (2022) Discovery, total syntheses and potent anti-inflammatory activity of pyrrolinone-fused benzoazepine alkaloids Asperazepanones A and B from Aspergillus candidus. Communications Chemistry. 5: 80
Zheng YY, Ma ZL, Wu JS, et al. (2022) Induction of Secondary Metabolite Biosynthesis by Deleting the Histone Deacetylase HdaA in the Marine-Derived Fungus RA2905. Journal of Fungi (Basel, Switzerland). 8
Jiang YY, Gao Y, Liu JY, et al. (2022) Design and Characterization of a Natural Arf-GEFs Inhibitor Prodrug with Potent Anti-Hepatocellular Carcinoma Efficacy . Journal of Medicinal Chemistry. 65: 11970-11984
Wang CF, Ma J, Jing QQ, et al. (2022) Integrating Activity-Guided Strategy and Fingerprint Analysis to Target Potent Cytotoxic Brefeldin A from a Fungal Library of the Medicinal Mangrove . Marine Drugs. 20
Jiang YY, Wu S, Wu YW, et al. (2022) New brefeldin A-cinnamic acid ester derivatives as potential antitumor agents: Design, synthesis and biological evaluation. European Journal of Medicinal Chemistry. 240: 114598
Wang CY, Liu XH, Zheng YY, et al. (2022) 2,5-Diketopiperazines From a Sponge-Derived Fungus . Frontiers in Microbiology. 13: 808532
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