Design, synthesis and biological evaluation of novel flavone Mannich base derivatives as potential antibacterial agents

2018 ◽  
Vol 23 (2) ◽  
pp. 299-306 ◽  
Author(s):  
Xian-Hai Lv ◽  
Hao Liu ◽  
Zi-Li Ren ◽  
Wei Wang ◽  
Feng Tang ◽  
...  
Keyword(s):  
Antibacterial Agents ◽  
Mannich Base ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
Synthesis And Biological Evaluation

Design, Synthesis, and Biological Evaluation of Hexacyclic Tetracyclines as Potent, Broad Spectrum Antibacterial Agents

2015 ◽  
Vol 58 (11) ◽  
pp. 4703-4712 ◽  
Author(s):  
Cuixiang Sun ◽  
Diana K. Hunt ◽  
Chi-Li Chen ◽  
Yonghong Deng ◽  
Minsheng He ◽  
...  
Keyword(s):  
Broad Spectrum ◽  
Antibacterial Agents ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
Synthesis And Biological Evaluation

ChemInform Abstract: Design, Synthesis, and Biological Evaluation of Indolylidinepyrazolones as Potential Antibacterial Agents.

ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
A. Indrasena ◽  
Sd. Riyaz ◽  
Prema L. Mallipeddi ◽  
P. Padmaja ◽  
B. Sridhar ◽  
...  
Keyword(s):  
Antibacterial Agents ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
Synthesis And Biological Evaluation

scholarly journals LpxC Inhibitors: Design, Synthesis, and Biological Evaluation of Oxazolidinones as Gram-negative Antibacterial Agents

2016 ◽  
Vol 7 (6) ◽  
pp. 623-628 ◽  
Author(s):  
Haruaki Kurasaki ◽  
Kosuke Tsuda ◽  
Mariko Shinoyama ◽  
Noriko Takaya ◽  
Yuko Yamaguchi ◽  
...  
Keyword(s):  
Antibacterial Agents ◽  
Biological Evaluation ◽  
Design Synthesis ◽  
Gram Negative ◽  
Synthesis And Biological Evaluation

Design, synthesis and biological evaluation of 5′-C-piperidinyl-5′-O-aminoribosyluridines as potential antibacterial agents

2015 ◽  
Vol 13 (28) ◽  
pp. 7720-7735 ◽  
Author(s):  
Takeshi Nakaya ◽  
Akira Matsuda ◽  
Satoshi Ichikawa
Keyword(s):  
Antibacterial Activity ◽  
Antibacterial Agents ◽  
Biological Evaluation ◽  
Human Cells ◽  
Ritter Reaction ◽  
Design Synthesis ◽  
Synthesis And Biological Evaluation

Caprazamycin analogues, which were designed and synthesized via an aza-Prins–Ritter reaction, exhibit a good MraY and antibacterial activity without cytotoxicity against human cells.

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