ChemInform Abstract: Total Synthesis of Marine Natural Products Driven by Novel Structure, Potent Biological Activity, and/or Synthetic Methodology

ChemInform ◽  
2001 ◽  
Vol 32 (11) ◽  
pp. no-no
Author(s):  
D. Romo ◽  
R. M. Rzasa ◽  
W. D. Schmitz ◽  
J. Yang ◽  
S. T. Cohn ◽  
...  
Marine Drugs ◽  
2019 ◽  
Vol 17 (7) ◽  
pp. 384 ◽  
Author(s):  
Qinxue Jing ◽  
Xu Hu ◽  
Yanzi Ma ◽  
Jiahui Mu ◽  
Weiwei Liu ◽  
...  

Marine natural products are considered to be valuable resources that are furnished with diverse chemical structures and various bioactivities. To date, there are seven compounds derived from marine natural products which have been approved as therapeutic drugs by the U.S. Food and Drug Administration. Numerous bromotyrosine derivatives have been isolated as a type of marine natural products. Among them, psammaplin A, including the oxime groups and carbon–sulfur bonds, was the first identified symmetrical bromotyrosine-derived disulfide dimer. It has been found to have a broad bioactive spectrum, especially in terms of antimicrobial and antiproliferative activities. The highest potential indole-derived psammaplin A derivative, UVI5008, is used as an epigenetic modulator with multiple enzyme inhibitory activities. Inspired by these reasons, psammaplin A has gradually become a research focus for pharmacologists and chemists. To the best of our knowledge, there is no systematic review about the biological activity and structural modification of psammaplin A. In this review, the pharmacological effects, total synthesis, and synthesized derivatives of psammaplin A are summarized.


2017 ◽  
Vol 15 (22) ◽  
pp. 4842-4850 ◽  
Author(s):  
Subhendu Das ◽  
Rajib Kumar Goswami

2009 ◽  
Vol 74 (6) ◽  
pp. 887-900 ◽  
Author(s):  
Álvaro Enríquez-García ◽  
Steven V. Ley

The bengazoles are marine natural products with unique structure, containing two oxazole rings flanking a single carbon. They show very potent antifungal activity. The total syntheses of bengazole C and E are described following a convergent route which involves diastereoselective cycloaddition of an appropriately substituted nitrile oxide with a butane-1,2-diacetal-protected alkenediol as the key step.


Author(s):  
Qian Wang ◽  
Jie-Ping Zhu ◽  
Kyriacos C. Nicolaou ◽  
Henry N. C. Wong ◽  
Wei-Dong Li

1982 ◽  
Vol 13 (13) ◽  
Author(s):  
A. G. GONZALEZ ◽  
J. D. MARTIN ◽  
C. PEREZ ◽  
M. A. RAMIREZ ◽  
F. RAVELO

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