49773-26-4Relevant articles and documents
In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis
Deb, Pran Kishore,Al-Shar’i, Nizar A.,Venugopala, Katharigatta N.,Pillay, Melendhran,Borah, Pobitra
, p. 869 - 884 (2021/06/11)
The alarming increase in multi- and extensively drug-resistant (MDR and XDR) strains of Mycobacterium tuberculosis (MTB) has triggered the scientific community to search for novel, effective, and safer therapeutics. To this end, a series of 3,5-disubstitu
Design, microwave assisted synthesis and characterization of substituted 1,2,4-oxadiazole analogues as promising pharmacological agents
Venugopala, Katharigatta N.
, p. 1767 - 1770 (2017/06/27)
Microwave assisted synthesis of a series of 3,5-disubstituted-1,2,4-oxadiazole analogues (3a-j) has been achieved between 5-(chloromethyl)-3-substituted phenyl-1,2,4-oxadiazoles (2a-j) and substituted benzophenone in presence of potassium carbonate in ace
1,2,4-Oxadiazoles. IV. Synthesis and pharmacological properties of a series of substituted aminoalkyl-1,2,4-oxadiazoles.
PALAZZO,TAVELLA,STRANI,SILVESTRINI
, p. 351 - 367 (2007/10/05)
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