马淑涛山东大学主页平台管理系统--中文主页

论文成果

[11] 马仰春. Exploration of the inhibitory mechanism of PC190723 on FtsZ protein by molecular dynamics simula.... 《JOURNAL OF MOLECULAR GRAPHICS & MODELLING》, 108189, 2022.
[12] 宋迪. Acridinium-conjugated aromatic heterocycles as highly potent FtsZ inhibitors: Design, synthesis, .... 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: .... European Journal of Medicinal Chemistry, 113723, 2021.
[15] 宋迪. Design, synthesis and evaluation of novel 9-arylalkyl-10-methylacridinium derivatives as highly p.... 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 synth.... 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.... 9, 2020.
[20] 刘兴邦. Total Synthesis of Semaglutide Based on a Soluble Hydrophobic-Support-Assisted Liquid-Phase Synth.... 22, 821, 2020.

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马淑涛

教授

性别：男

在职信息：在职

所在单位：药学院

入职时间： 2002-11-19

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