Synthesis, biological activity and structure–activity relationship of endomorphin-1/substance P derivatives

2012 ◽  
Vol 20 (21) ◽  
pp. 6335-6343 ◽  
Author(s):  
Pegah Varamini ◽  
Waleed M. Hussein ◽  
Friederike M. Mansfeld ◽  
Istvan Toth
2000 ◽  
Vol 53 (12) ◽  
pp. 909 ◽  
Author(s):  
Yoshikazu Hiraga ◽  
Mariko Ago ◽  
Munetaka Tokumasu ◽  
Ken Kaku ◽  
Katsuo Ohkata

Analogues of hippospongic acid A, which inhibit the gastrulation of sea urchin embryos, were synthesized. From a study on structure—activity relationships, the conjugated carboxylic acid moiety was found to be an essential feature for biological activity.


2014 ◽  
Vol 71 (7) ◽  
pp. 928-936 ◽  
Author(s):  
Benjamin M Nugent ◽  
Ann M Buysse ◽  
Michael R Loso ◽  
Jon M Babcock ◽  
Timothy C Johnson ◽  
...  

2013 ◽  
Vol 411-414 ◽  
pp. 3158-3161 ◽  
Author(s):  
Yu Bin Ji ◽  
Yan Dong ◽  
Ning Chen ◽  
Dong Xue Song ◽  
Jia Zheng

This paper reviews the structure-activity relationship of two typical Amaryllidaceae isocarbostyril alkaloids, narciclasine, pancratistatin and their derivatives. Varieties structures have important impacts on biological activity of Amaryllidaceae isocarbostyril alkaloids, for example, the nuclear structure of isocarbostyril, the stereochemistry of the B/C ring junction, the C7-hydroxy of ring A, hydroxies of ring C and so on. This study is conducive to find other active groups, conduct structural modifications and provide the rational basis for designing drugs molecular.


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