Synthesis and Anticancer Evaluation of N-(Pyridin-3-yl)benzamide Derivatives

2021 ◽  
Vol 57 (9) ◽  
pp. 1495-1500
Author(s):  
G. Mohan ◽  
G. Sridhar ◽  
E. Laxminarayana ◽  
M. T. Chary
ChemInform ◽  
2010 ◽  
Vol 26 (45) ◽  
pp. no-no
Author(s):  
S. KATO ◽  
T. MORIE ◽  
K. OHNO ◽  
N. YOSHIDA ◽  
T. YOSHIDA ◽  
...  

2015 ◽  
Vol 6 (5) ◽  
pp. 607-611 ◽  
Author(s):  
Mohammad A. Khanfar ◽  
Luisa Quinti ◽  
Hua Wang ◽  
Johnathan Nobles ◽  
Aleksey G. Kazantsev ◽  
...  

2014 ◽  
Vol 52 (6) ◽  
pp. 1848-1857 ◽  
Author(s):  
Banafshe Samani Ghaleh Taki ◽  
Mahbubeh Rostami ◽  
Valiollah Mirkhani ◽  
Majid Moghadam ◽  
Iraj Mohammadpoor-Baltork ◽  
...  

2019 ◽  
Vol 41 (3) ◽  
pp. 549-549
Author(s):  
Xuesong Wang and Xiaorong Tang Xuesong Wang and Xiaorong Tang

A series of novel benzamide derivatives according to fluopicolide were designed and synthesized following the rule of combination carboxylic acid amides and amines derivatives together. The antifungal activity of the 15 new compounds were evaluated in vitro against five pathogenic fungi, including Sclerotinia sclerotiorum, Gibberella zeae, Rhizoctonia solani, Helminthosporium maydis and Botrytis cinerea. Almost all the structure have not been reported, except compounds 3, 5 and 6. A surprising finding is that all the five tested fungi breed faster than negative controls when supplementary with compound 715 , respectively.


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