Synthesis and biological evaluation of strigol analogues modified in the enol ether part

1997 ◽  
pp. 767-774 ◽  
Author(s):  
Jan Willem ◽  
J. F. Thuring ◽  
Angelique A. M. A. van Gaal ◽  
Sander J. Hornes ◽  
Margreet M. de Kok ◽  
...  
Keyword(s):  
Biological Evaluation ◽  
Enol Ether ◽  
Synthesis And Biological Evaluation

ChemInform Abstract: Synthesis and Biological Evaluation of Strigol Analogues Modified in the Enol Ether Part.

ChemInform ◽  
2010 ◽  
Vol 28 (35) ◽  
pp. no-no
Author(s):  
J. W. J. F. THURING ◽  
A. A. M. A. VAN GAAL ◽  
S. J. HORNES ◽  
M. M. DE KOK ◽  
G. H. L. NEFKENS ◽  
...  
Keyword(s):  
Biological Evaluation ◽  
Enol Ether ◽  
Synthesis And Biological Evaluation

Synthesis and Biological Evaluation of the Antimicrobial Natural Product Lipoxazolidinone A

2018 ◽  
Author(s):  
Jonathan J. Mills ◽  
Kaylib R. Robinson ◽  
Troy E. Zehnder ◽  
Joshua G. Pierce
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Mechanism Of Action ◽  
Marine Natural Products ◽  
Biological Evaluation ◽  
Lead Compounds ◽  
Follow Up Studies ◽  
Initial Resistance ◽  
Synthesis And Biological Evaluation

The lipoxazolidinone family of marine natural products, with an unusual 4-oxazolidinone heterocycle at their core, represents a new scaffold for antimicrobial discovery; however, questions regarding their mechanism of action and high lipophilicity have likely slowed follow-up studies. Herein, we report the first synthesis of lipoxazolidinone A, 15 structural analogs to explore its active pharmacophore, and initial resistance and mechanism of action studies. These results suggest that 4-oxazolidinones are valuable scaffolds for antimicrobial development and reveal simplified lead compounds for further optimization.

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