Di Song
Qingdao, 266000, China
Last Updated: 09/26/2026
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Found 17 publications
Pan-Genome-Wide Investigation and Co-Expression Network Analysis of HSP20 Gene Family in Maize.
Journal: International journal of molecular sciences
Published: August 31, 2024
Acridinium-conjugated aromatic heterocycles as highly potent FtsZ inhibitors: Design, synthesis, and biological evaluation.
Journal: Archiv der Pharmazie
Published: October 13, 2021
Rational design and synthesis of Oreoch-2 analogues as efficient broad-spectrum antimicrobial peptides.
Journal: Bioorganic chemistry
Published: September 27, 2021
Modification of 5-methylphenanthridium from benzothiazoles to indoles as potent FtsZ inhibitors: Broadening the antibacterial spectrum toward vancomycin-resistant enterococci.
Journal: European journal of medicinal chemistry
Published: May 23, 2021
Design, synthesis and evaluation of novel 9-arylalkyl-10-methylacridinium derivatives as highly potent FtsZ-targeting antibacterial agents.
Journal: European journal of medicinal chemistry
Published: March 26, 2021
Antimicrobial Action and Reversal of Resistance in MRSA by Difluorobenzamide Derivatives Targeted at FtsZ.
Journal: Antibiotics (Basel, Switzerland)
Published: October 16, 2020
Total Synthesis of Semaglutide Based on a Soluble Hydrophobic-Support-Assisted Liquid-Phase Synthetic Method.
Journal: ACS combinatorial science
Published: October 15, 2020
Design and synthesis of novel 4-substituted quinazoline-2-carboxamide derivatives targeting AcrB to reverse the bacterial multidrug resistance.
Journal: Bioorganic chemistry
Published: June 06, 2020
Design, synthesis of novel 4,5-dihydroisoxazole-containing benzamide derivatives as highly potent FtsZ inhibitors capable of killing a variety of MDR Staphylococcus aureus.
Journal: Bioorganic & medicinal chemistry
Published: June 03, 2020
A novel series of 11-O-carbamoyl-3-O-descladinosyl clarithromycin derivatives bearing 1,2,3-triazole group: Design, synthesis and antibacterial evaluation.
Journal: Bioorganic & medicinal chemistry letters
Published: September 11, 2019
Structural optimization of natural product nordihydroguaretic acid to discover novel analogues as AcrB inhibitors.
Journal: European journal of medicinal chemistry
Published: August 13, 2019
Discovery of 1,3,4-oxadiazol-2-one-containing benzamide derivatives targeting FtsZ as highly potent agents of killing a variety of MDR bacteria strains.
Journal: Bioorganic & medicinal chemistry
Published: March 06, 2019
Last Updated: 09/26/2026