2015
DOI: 10.1016/j.bmcl.2015.03.027
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Synthesis and biological evaluation of 2-arylbenzimidazoles targeting Leishmania donovani

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Cited by 15 publications
(17 citation statements)
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“…The developed synthesis route to carboxyimidamide-substituted benzo[c] [1,2,5]oxadiazoles and related derivatives facilitates access to a compound library and determination of the structure-activity relationships for this antileishmanial heterocyclic chemotype. Carboxyimidamidesubstituted benzoxadiazole derivative 14 is the most promising compound of this study, demonstrating good antileishmanial inhibition activity in infected macrophages and, remarkably, no signs of cytotoxicity.…”
Section: Resultsmentioning
confidence: 99%
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“…The developed synthesis route to carboxyimidamide-substituted benzo[c] [1,2,5]oxadiazoles and related derivatives facilitates access to a compound library and determination of the structure-activity relationships for this antileishmanial heterocyclic chemotype. Carboxyimidamidesubstituted benzoxadiazole derivative 14 is the most promising compound of this study, demonstrating good antileishmanial inhibition activity in infected macrophages and, remarkably, no signs of cytotoxicity.…”
Section: Resultsmentioning
confidence: 99%
“…Initially, benzo[c] [1,2,5] The reaction of the obtained primary amide 3 with trifluoroacetic anhydride and Et 3 N in THF 9 gave the corresponding nitrile 4, which was converted to the amidoxime 5 by using hydroxylamine hydrochloride 10 in the presence of Et 3 N in EtOH. The final step to obtain the derivatives (6-18, 24) was carried out in the presence of the substituted phenyl isocyanates in THF or CHCl 3 .…”
Section: Chemistrymentioning
confidence: 99%
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