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dc.contributor.authorKundu, Mrinal K-
dc.contributor.authorThomas, Jacob V-
dc.contributor.authorBhat, Sujata V-
dc.date.accessioned2013-03-29T20:33:53Z-
dc.date.available2013-03-29T20:33:53Z-
dc.date.issued1999-11-
dc.identifier.urihttp://hdl.handle.net/123456789/16663-
dc.description1299-1300en_US
dc.description.abstractMalaria has become a serious disease throughout recorded history and the protozoan parasite of the family Plasmodidae is known to be the etiologic agent for this. The dangerously improved immunological status of various parasites (especially human malaria parasite P. falciparum) against conventional drugs such as chloroquine necessitates the development of new agents having optimum efficacy.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(11) [November 1999]en_US
dc.titleMonoterpenic fragment analogues of Aplasmomycin as potential anti-malarialsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(11) [November 1999]

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