马淑涛
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Gender:Male
Paper Publications
- [11] 马仰春. Exploration of the inhibitory mechanism of PC190723 on FtsZ protein by molecular dynamics simulation. 《JOURNAL OF MOLECULAR GRAPHICS & MODELLING》, 108189, 2022.
- [12] 宋迪. Acridinium-conjugated aromatic heterocycles as highly potent FtsZ inhibitors: Design, synthesis, and biological evaluation. Archiv der Pharmazie, 2022.
- [13] 马银刚. Redox deracemization of diarylmethyl alkynes. Organic Chemistry Frontiers, 2020.
- [14] 张楠. Modification of 5-methylphenanthridium from benzothiazoles to indoles as potent FtsZ inhibitors: Broadening the antibacterial spectrum toward vancomycin-resistant enterococci. European Journal of Medicinal Chemistry, 113723, 2021.
- [15] 宋迪. Design, synthesis and evaluation of novel 9-arylalkyl-10-methylacridinium derivatives as highly potent FtsZ-targeting antibacterial agents. European Journal of Medicinal Chemistry, 221, 2021.
- [16] 张娜. Development of novel synthetic method of natural antimicrobial peptide TP4. Tetrahedron Letters, 79, 2021.
- [17] 刘兴邦. Total synthesis of semaglutide based on a soluble hydrophobic-support-assisted liquid-phase synthetic method. ACS Combinatorial Science, 22, 821, 2020.
- [18] 刘志阳. Design and synthesis of aryl-substituted pyrrolidone derivatives as quorum sensing inhibitors. Bioorganic Chemistry, 104376, 2020.
- [19] Chai, Wern Chern. Antimicrobial Action and Reversal of Resistance in MRSA by Difluorobenzamide Derivatives Targeted at FtsZ. 9, 2020.
- [20] 刘兴邦. Total Synthesis of Semaglutide Based on a Soluble Hydrophobic-Support-Assisted Liquid-Phase Synthetic Method. 22, 821, 2020.