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Organic & Biomolecular Chemistry|December 4, 2023
A novel synthetic method for backbone-cyclized polypeptide POL7080 with the help of hydrophobic-support materialsXiaotong Gu, Weijin Chen, Ting Guo, et al.
Archiv Der Pharmazie|March 10, 2022
Acridinium-conjugated aromatic heterocycles as highly potent FtsZ inhibitors: Design, synthesis, and biological evaluationDi Song, Nan Zhang, Yangchun Ma, et al.
European Journal of Medicinal Chemistry|August 2, 2021
Modification of 5-methylphenanthridium from benzothiazoles to indoles as potent FtsZ inhibitors: Broadening the antibacterial spectrum toward vancomycin-resistant enterococciNan Zhang, Di Song, Weijin Chen, et al.
Bioorganic & Medicinal Chemistry Letters|June 9, 2018
Synthesis and antibacterial evaluation of novel 11-O-aralkylcarbamoyl-3-O-descladinosylclarithromycin derivativesLi Jia, Yinhu Wang, Yanxia Wang, et al.
Bioorganic Chemistry|October 25, 2020
Design and synthesis of aryl-substituted pyrrolidone derivatives as quorum sensing inhibitorsZhiyang Liu, Panpan Zhang, Yinhui Qin, et al.
Bioorganic & Medicinal Chemistry|October 16, 2020
Design, synthesis of novel 4,5-dihydroisoxazole-containing benzamide derivatives as highly potent FtsZ inhibitors capable of killing a variety of MDR Staphylococcus aureusDi Song, Fangchao Bi, Nan Zhang, et al.
ACS Combinatorial Science|October 15, 2020
Total Synthesis of Semaglutide Based on a Soluble Hydrophobic-Support-Assisted Liquid-Phase Synthetic MethodXingbang Liu, Na Zhang, Xiaotong Gu, et al.
The Journal of Antibiotics|February 16, 2012
WITHDRAWN: Novel azithromycin derivatives with the C-4″ bisamide side chains: synthesis and biological evaluation against gram-positive bacteriaWenping Cui, Lihong An, Chenchen Ma, et al.
Bioorganic & Medicinal Chemistry Letters|June 22, 2017
Synthesis and antibacterial activity of 5-methylphenanthridium derivatives as FtsZ inhibitorsFang Liu, Henrietta Venter, Fangchao Bi, et al.
Bioorganic & Medicinal Chemistry Letters|January 14, 2017
Design, synthesis and biological activity evaluation of novel 2,6-difluorobenzamide derivatives through FtsZ inhibitionFangchao Bi, Liwei Guo, Yinhu Wang, et al.
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