Orally active esters of dihydroartemisinin: Synthesis and antimalarial activity against multidrug-resistant Plasmodium yoelii in mice.

Abstract:

:A series of artemisinin derived esters 7a-j, incorporating pharmacologically privileged substructure, such as biphenyl, adamantane and fluorene, have been prepared and evaluated for antimalarial activity against multidrug-resistant (MDR) Plasmodium yoelii nigeriensis by oral route. Several of these compounds were found to be more active than the antimalarial drugs beta-arteether 4 and artesunic acid 5. Ester 7i, the most active compound of the series, provided 100% and 80% protection to the infected mice at 24 mg/kg x 4 days and 12 mg/kg x 4 days, respectively. In this model beta-arteether provided 100% and 20% protection at 48 mg/kg x 4 days and 24 mg/kg x 4 days, respectively.

journal_name

Bioorg Med Chem Lett

authors

Singh C,Chaudhary S,Puri SK

doi

10.1016/j.bmcl.2007.12.074

subject

Has Abstract

pub_date

2008-02-15 00:00:00

pages

1436-41

issue

4

eissn

0960-894X

issn

1464-3405

pii

S0960-894X(08)00003-6

journal_volume

18

pub_type

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