scholarly journals Structure-activity relationship study of human interleukin-3. Identification of residues required for biological activity by site-directed mutagenesis

1991 ◽  
Vol 266 (16) ◽  
pp. 10624-10631
Author(s):  
N.A. Lokker ◽  
N.R. Movva ◽  
U. Strittmatter ◽  
B. Fagg ◽  
G. Zenke
Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3433 ◽  
Author(s):  
Anastasia Khandazhinskaya ◽  
Elena Matyugina ◽  
Pavel Solyev ◽  
Maggie Wilkinson ◽  
Karen Buckheit ◽  
...  

Carbocyclic nucleosides have long played a role in antiviral, antiparasitic, and antibacterial therapies. Recent results from our laboratories from two structurally related scaffolds have shown promising activity against both Mycobacterium tuberculosis and several parasitic strains. As a result, a small structure activity relationship study was designed to further probe their activity and potential. Their synthesis and the results of the subsequent biological activity are reported herein.


1995 ◽  
Vol 73 (4) ◽  
pp. 550-557 ◽  
Author(s):  
Anmar K. Mohammed-Ali ◽  
Tak-Hang Chan ◽  
Anthony W. Thomas ◽  
George M. Strunz ◽  
Brent Jewett

A quantitative structure–activity relationship study was performed for a number of aroylhydrazine compounds with respect to their biological activity against spruce budworm. It was found that the biological activity can be modulated by substituents on the aromatic rings. Substituents with high π value and small L value lead to increase in biological activity. Molecular mechanics calculations were used to explain how the active compounds may mimic the strong-binding Y region of ecdysone. Keywords: spruce budworm, ecdysone, agonist, hydrazines, quantitative structure–activity relationship.


1994 ◽  
Vol 14 (1) ◽  
pp. 51-60 ◽  
Author(s):  
Mariagrazia Pizza ◽  
Mario Domenighini ◽  
Wim Hol ◽  
Valentine Giannelli ◽  
Maria Rita Fontana ◽  
...  

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