52334-57-3Relevant academic research and scientific papers
Synthesis and antibacterial activity of some N-(3-hydroxy-2-pyridyl) benzamides
Mobinikhaledi,Forughifar,Shariatzadeh,Fallah
, p. 427 - 430 (2008/02/12)
N-(3-Hydroxy-2-pyridyl)benzamides 3(a-J) were synthesized under weak basic solution by reacting of 2-amino-3-pyridinol and an appropriate carboxylic acid chloride, obtained by reaction of carboxylic acids with thionyl chloride. The microbiological activity of these compounds was tested in vitro against Escherichia Coil (PTCC 1338), Pseudomonas aeruginosa (PTCC 1074), Entrococcus faecalis (PTCC 1237) and Staphylococcus aureus (PTCC 1119) bacteria. Compounds 3a, 3e and 3f were the active benzamide derivatives against the Ef and Sa bacteria with a MIC value of 128 μg/ml. Compound 3g was the active entry against Ec and Pa bacteria with a MIC value of 128 μg/.
Synthesis of some N1-(3-hydroxy-2-pyridyl)benzamides
Mobinikhaledi,Foroughifar,Fallah
, p. 717 - 721 (2007/10/03)
Benzoxazoles are of special interest because of having various types of biological properties such as antihistaminic, antihelmintic antifungal and antibacterial activities.1-10 Benzamide derivatives, as the possible metabolites of benzoxazoles,
Anti-inflammatory oxazole[4,5-b]pyridines
-
, (2008/06/13)
The various isomers of oxazolo- and thiazolopyridines having utility as antiinflammatory, antipyretic and analgesic agents are prepared by condensation of an appropriate amino-hydroxypyridine or amino-mercaptopyridine with a carboxylic acid, halide or anhydride.
