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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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