Structural optimization of natural product fusaric acid to discover novel T3SS inhibitors of Salmonella

Author(s):  
Yuliang Song ◽  
Guangsen Xu ◽  
Chaoqun Li ◽  
Zhiying Li ◽  
Chunhua Lu ◽  
...  
2008 ◽  
Vol 16 (18) ◽  
pp. 8635-8642 ◽  
Author(s):  
Simone Di Micco ◽  
Stefania Terracciano ◽  
Ines Bruno ◽  
Manuela Rodriquez ◽  
Raffaele Riccio ◽  
...  

2020 ◽  
Vol 186 ◽  
pp. 111910 ◽  
Author(s):  
Yinhu Wang ◽  
Rawaf Alenzy ◽  
Di Song ◽  
Xingbang Liu ◽  
Yuetai Teng ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 3859
Author(s):  
Bin Bin Huang ◽  
Ya Yi Liu ◽  
Peng Fei Zhu ◽  
Yi Cheng Jiang ◽  
Ming-An Ouyang

The total synthesis of a natural product alkaloid fusaric acid (FA), which exhibits herbicide, fungicide, insecticide and even diverse notable pharmacological activities, was accomplished in four steps using commercially available materials. The synthesis, based on a unified and flexible strategy using 6-bromonicotinaldehyde as a common intermediate, is concise, convergent, practical and can be carried out on a two-gram scale. This approach could be readily applicable to the synthesis of its analogues. In addition, FA had a wide range of inhibitory activities against 14 plant pathogenic fungi in this study, which demonstrated that as a leading compound, and it has great potential to be further developed as an agricultural fungicide.


Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
V Myrianthopoulos ◽  
P Magiatis ◽  
AL Skaltsounis ◽  
L Meijer ◽  
E Mikros

Planta Medica ◽  
2012 ◽  
Vol 78 (05) ◽  
Author(s):  
SK Jain ◽  
R Sahu ◽  
J Zhang ◽  
MR Jacob ◽  
XC Li ◽  
...  

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