山东大学教师主页马淑涛论文成果中文主页

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论文成果

[11] 张玲. Synthesis and antibacterial activity of new 4 ''-O-carbamates of 11,12-cyclic carbonate erythromycin A 6,9-imino ether. JOURNAL OF ANTIBIOTICS, 64, 243-247, 2011.
[12] 张娜. Rational design and synthesis of Oreoch-2 analogues as efficient broad-spectrum antimicrobial peptides. Bioorganic Chemistry, 105583, 2022.
[13] 顾晓彤. Recent Advances in the Development of Pyrazolopyridines as Anticancer Agents. Anti-cancer agents in medicinal chemistry, 1640, 2022.
[14] 马仰春. Exploration of the inhibitory mechanism of PC190723 on FtsZ protein by molecular dynamics simulation. 《JOURNAL OF MOLECULAR GRAPHICS & MODELLING》, 108189, 2022.
[15] 宋迪. Acridinium-conjugated aromatic heterocycles as highly potent FtsZ inhibitors: Design, synthesis, and biological evaluation. Archiv der Pharmazie, 2022.
[16] 马银刚. Redox deracemization of diarylmethyl alkynes. Organic Chemistry Frontiers, 2020.
[17] 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.
[18] 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.
[19] 张娜. Development of novel synthetic method of natural antimicrobial peptide TP4. Tetrahedron Letters, 79, 2021.
[20] 刘兴邦. Total synthesis of semaglutide based on a soluble hydrophobic-support-assisted liquid-phase synthetic method. ACS Combinatorial Science, 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

所属院系：齐鲁医学院 , 药学院 , 药学院 , 药学院

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