scholarly journals Structure-activity Relationship of 1.BETA.-Methyl-carbapenem to Its Antibacterial Activity: Effectof the C-2 Side Chain and the 1.BETA.-Methyl Group.

1996 ◽  
Vol 49 (11) ◽  
pp. 1175-1178 ◽  
Author(s):  
MAKOTO SUNAGAWA ◽  
HARUKI MATSUMURA ◽  
AKIRA SASAKI ◽  
HIROSHI YAMAGA ◽  
YOSHIHIRO SUMITA ◽  
...  
2012 ◽  
Vol 9 (3) ◽  
pp. 329-335 ◽  
Author(s):  
Surajit Kumar Ghosh ◽  
Ashmita Saha ◽  
Bornali Hazarika ◽  
Udaya Pratap Singh ◽  
Hans Raj Bhat ◽  
...  

Polymer ◽  
2000 ◽  
Vol 41 (2) ◽  
pp. 415-421 ◽  
Author(s):  
N Tirelli ◽  
A Altomare ◽  
R Solaro ◽  
F Ciardelli ◽  
S Follonier ◽  
...  

2019 ◽  
Vol 16 (2) ◽  
pp. e1800560 ◽  
Author(s):  
Yun-Ge Li ◽  
Ju-Xian Wang ◽  
Guo-Ning Zhang ◽  
Mei Zhu ◽  
Xue-Fu You ◽  
...  

2008 ◽  
Vol 61 (2) ◽  
pp. 98-102 ◽  
Author(s):  
Ikuko Kozone ◽  
Makoto Hashimoto ◽  
Udo Gräfe ◽  
Hiroshi Kawaide ◽  
Hiroshi Abe ◽  
...  

2001 ◽  
Vol 56 (11-12) ◽  
pp. 1029-1037 ◽  
Author(s):  
Masahiro Miyashita ◽  
Tomoko Nakamori ◽  
Takahiro Murai ◽  
Tetsuro Yonemoto ◽  
Hisashi Miyagawa ◽  
...  

Abstract AM -toxins are host-specific phytotoxins of the Alternaria alternata apple pathotype, which induce necrosis on apple leaves. In this study, we developed a new assay to measure the necrotic activity of AM -toxin analogs using cultured leaves from meristem cells. This method was not only more sensitive to AM -toxin I, but also more reliable than the previous one that used tree leaves due to the homogeneous nature of cultured leaves and to the method of application of toxins. U sing this assay method we investigated a structure-activity relationship of AM -toxin analogs synthesized in this study. Most residues and the macrocyclic ring structure were strictly recognized by AM -toxin putative receptor, whereas the L-Ala binding subsite of the receptor allowed for side chain structures with various stereoelectronic properties. These findings are important for designing ligands for further experimental probing of the nature of the receptor.


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