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[1] The semi-synthesis, biological evaluation and docking analysis of the oxime, hydrazine and hydrazide derivatives of platensimycin [J]. MedChemComm, 2018,
[2] Semisynthesis of platensimycin derivatives with antibiotic activities in mice via Suzuki–Miyaura cross-coupling reactions [J]. Journal of medicinal chemistry, 2018,
[3] Late-stage functionalization of platensimycin leading to multiple analogues with improved antibacterial activity in vitro and in vivo [J]. Journal of medicinal chemistry, 2019,
[4] Novel bisubstrate inhibitors for protein N-terminal acetyltransferase D [J]. Journal of medicinal chemistry, 2021,
[5] Morphing Natural Product Platensimycin via Heck, Sonogashira, and One-Pot Sonogashira/Cycloaddition Reactions to Produce Antibiotics with In Vivo Activity [J]. Antibiotics, 2022,
[6] Venglustat inhibits protein N-terminal methyltransferase 1 in a substrate-competitive manner [J]. Journal of Medicinal Chemistry, 2022,
[7] Structure–activity relationship studies of Venglustat on NTMT1 inhibition [J]. Journal of Medicinal Chemistry, 2023,
[8] Comparative Study of Adenosine Analogs as Inhibitors of Protein Arginine Methyltransferases and a Clostridioides difficile-Specific DNA Adenine Methyltransferase [J]. ACS Chemical Biology, 2023,
[9] Venglustat Analogues with Enhanced Inhibition for Protein N-Terminal Methyltransferases 1/2 [J]. Journal of Pharmacology and Experimental Therapeutics 385 (S3), 2023,
[10] A unique binding pocket induced by a noncanonical SAH mimic to develop potent and selective PRMT inhibitors [J]. Acta Pharmaceutica Sinica B, 2023,
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