Design, synthesis and anti-inflammatory activity of 3-amino acid derivatives of ocotillol-type sapogenins

2020 ◽  
Vol 202 ◽  
pp. 112507 ◽  
Author(s):  
Gangqiang Yang ◽  
Meng Gao ◽  
Yixiao Sun ◽  
Conghui Wang ◽  
Xiaojuan Fang ◽  
...  
2014 ◽  
Vol 14 (7) ◽  
pp. 984-993 ◽  
Author(s):  
Gabriela Luna-Palencia ◽  
Federico Martinez-Ramos ◽  
Ismael Vasquez-Moctezuma ◽  
Manuel Fragoso-Vazquez ◽  
Jessica Mendieta-Wejebe ◽  
...  

2014 ◽  
Vol 347 (11) ◽  
pp. 786-797 ◽  
Author(s):  
Vladimir Dobričić ◽  
Bojan Marković ◽  
Nikola Milenković ◽  
Vladimir Savić ◽  
Vesna Jaćević ◽  
...  

2015 ◽  
Vol 11 (8) ◽  
pp. 753-763 ◽  
Author(s):  
Kaliappan Ilango ◽  
Parthiban Valentina ◽  
Gajendra Kumar ◽  
Dushyant Dixit ◽  
Shrikant Nilewar ◽  
...  

1978 ◽  
Vol 12 (9) ◽  
pp. 1150-1153 ◽  
Author(s):  
N. M. Divanyan ◽  
S. A. Kazaryan ◽  
L. Kh. Galstyan ◽  
O. L. Mndzhoyan ◽  
V. G. Sarkisyan ◽  
...  

2012 ◽  
Vol 47 ◽  
pp. 52-58 ◽  
Author(s):  
Hélio A. Stefani ◽  
Giancarlo V. Botteselle ◽  
Julio Zukerman-Schpector ◽  
Ignez Caracelli ◽  
Denis da Silva Corrêa ◽  
...  

Author(s):  
Tian-Yi Zhang ◽  
Chun-Shi Li ◽  
Li-Ting Cao ◽  
Xue-Qian Bai ◽  
Dong-Hai Zhao ◽  
...  

2020 ◽  
Vol 88 (4) ◽  
pp. 57
Author(s):  
Oussama Moussaoui ◽  
Rajendra Bhadane ◽  
Riham Sghyar ◽  
El Mestafa El Hadrami ◽  
Soukaina El Amrani ◽  
...  

A new series of amino acid derivatives of quinolines was synthesized through the hydrolysis of amino acid methyl esters of quinoline carboxamides with alkali hydroxide. The compounds were purified on silica gel by column chromatography and further characterized by TLC, NMR and ESI-TOF mass spectrometry. All compounds were screened for in vitro antimicrobial activity against different bacterial strains using the microdilution method. Most of the synthesized amino acid-quinolines show more potent or equipotent inhibitory action against the tested bacteria than their correspond esters. In addition, many of them exhibit fluorescent properties and could possibly be utilized as fluorophores. Molecular docking and simulation studies of the compounds at putative bacterial target enzymes suggest that the antimicrobial potency of these synthesized analogues could be due to enzyme inhibition via their favorable binding at the fluoroquinolone binding site at the GyrA subunit of DNA gyrase and/or the ParC subunit of topoisomerase-IV.


1959 ◽  
Vol 81 (2) ◽  
pp. 377-382 ◽  
Author(s):  
L. R. Morris ◽  
R. A. Mock ◽  
C. A. Marshall ◽  
J. H. Howe

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