| 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 | |
| dc.contributor.author | Saxena, J K | |
| dc.contributor.author | Chauhan, P M S | |
| dc.date.accessioned | 2015-05-27T11:09:30Z | |
| dc.date.available | 2015-05-27T11:09:30Z | |
| dc.date.issued | 2014 | |
| 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 | |
| dc.format.mimetype | application/pdf | |
| 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 |