dc.contributor.author |
Sharma, Rashmi |
|
dc.contributor.author |
Pandey, A K |
|
dc.contributor.author |
Srivastava, Kumkum |
|
dc.contributor.author |
Puri, S K |
|
dc.contributor.author |
Singh, S V |
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dc.contributor.author |
Saxena, J K |
|
dc.contributor.author |
Chauhan, P M S |
|
dc.date.accessioned |
2015-05-27T11:09:30Z |
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dc.date.available |
2015-05-27T11:09:30Z |
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dc.date.issued |
2014 |
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dc.identifier.citation |
Chemistry & Biology Interface, 2014, 4(5), 268-280 |
en |
dc.identifier.uri |
http://hdl.handle.net/123456789/1533 |
|
dc.description.abstract |
Antimalarials based on the 4-aminoquinoline-schiff base hybrid coupled with oxalamide functionality as linker are designed and synthesized. The molecules were evaluated for their antiplasmodial activity against choroquine-resistant (CQ-R) K1 and choroquine-sensitive (CQ-S) 3D7 of Plasmodium falciparum strains. Some of the novel compounds were found to be more potent than Chloroquine in vitro against CQ-R strain. Furthermore several molecules also showed promising β-hematin inhibitory activity. |
en |
dc.format.extent |
226984 bytes |
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dc.format.mimetype |
application/pdf |
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dc.language.iso |
en |
en |
dc.relation.ispartofseries |
CSIR-CDRI Communication No. 8838 |
en |
dc.subject |
Antimalarial |
en |
dc.subject |
4-Aminoquinoline |
en |
dc.subject |
Drug resistance |
en |
dc.subject |
Oxalamide |
en |
dc.subject |
Schiff base |
en |
dc.title |
4-Aminoquinoline-Schiff base Hybrid: Rational Drug Design Approach for Overcoming Chloroquine Resistance in Malaria |
en |
dc.type |
Article |
en |