dc.contributor.author |
Verma, Aditya |
|
dc.contributor.author |
Srivastava, Saumya |
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dc.contributor.author |
Sane, S A |
|
dc.contributor.author |
Marrapu, V K |
|
dc.contributor.author |
Srinivas, Nagarapu |
|
dc.contributor.author |
Yadav, Manisha |
|
dc.contributor.author |
Bhandari, Kalpana |
|
dc.contributor.author |
Gupta, Suman |
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dc.date.accessioned |
2011-05-13T08:50:04Z |
|
dc.date.available |
2011-05-13T08:50:04Z |
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dc.date.issued |
2011 |
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dc.identifier.citation |
Acta Tropica 117(2), 11,157-60 |
en |
dc.identifier.uri |
http://hdl.handle.net/123456789/664 |
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dc.description.abstract |
Antileishmanial activities of 16 synthetic oximino benzocycloalkyl azoles against Leishmania donovani were evaluated in vitro against extracellular promastigotes and intracellular amastigotes. Based on SI (Selectivity Index), 5 compounds were tested further in vivo in hamster model. Out of these, three compounds have shown medium activity (53-58%) and one has shown significant inhibition of parasite multiplication (70%). Despite the fact that these compounds were better than the existing antileishmanials in respect to IC50 and SI values, they were less active than miltefosine in vivo . The present study has helped us in identifying a new lead that could be exploited as a potential antileishmanial agent. |
en |
dc.format.extent |
273066 bytes |
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dc.format.mimetype |
application/pdf |
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dc.language.iso |
en |
en |
dc.relation.ispartofseries |
cdricommunicationno.7993 |
en |
dc.subject |
Visceral leishmaniasis |
en |
dc.subject |
Antileishmanial activity |
en |
dc.subject |
benzocycloalkyl azole oximino ethers |
en |
dc.subject |
Luciferase assay |
en |
dc.title |
Antileishmanial activity of benzocycloalkyl azole oximino ethers: The conformationally constraint analogues of oxiconazole |
en |
dc.type |
Article |
en |