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Title: Development of 2,4-diaminopyrimidines as antimalarials based on inhibition of the S108N and C59R+S108N mutants of dihydrofolate reductase from pyrimethamine resistant Plasmodium falciparum
Authors: Bongkoch Tarnchompoo
Chawanee Sirichaiwat
Worrapong Phupong
Chakapong Intaraudom
Worachart Sirawaraporn
Sumalee Kamchonwongpaisan
Jarunee Vanichtanankul
Yodhathai Thebtaranonth
Yongyuth Yuthavong
Thailand National Center for Genetic Engineering and Biotechnology
Mahidol University
Keywords: Chemistry
Issue Date: 14-Mar-2002
Citation: Journal of Medicinal Chemistry. Vol.45, No.6 (2002), 1244-1252
Abstract: The reduced binding of pyrimethamine to Serl08Asn (S108N) mutants of parasite dihydrofolate reductase (DHFR), which forms the basis of resistance of Plasmodium falciparum to pyrimethamine, is largely due to steric constraint imposed by the bulky side chain of N108 on Cl of the 5-p-Cl-phenyl group. This and other S108 mutants with bulky side chains all showed reduced binding to pyrimethamine and cycloguanil. Less effect on binding to some bulky mutants was observed for trimethoprim, with greater flexibility for the 5-substituent. S108N DHFR also binds poorly with other pyrimethamine derivatives with bulky groups in place of the p-Cl, and the binding was generally progressively poorer for the double (C59R+S108N) mutant. Removal of the p-Cl or replacement with m-Cl led to better binding with the mutant DHFRs. Pyrimethamine analogues with unbranched hydrophobic 6-substituents showed generally good binding with the mutant DHFRs. A number of compounds were identified with high affinities for both wild-type and mutant DHFRs, with very low to no affinity to human DHFR. Some of these compounds show good antimalarial activities against pyrimethamine-resistant P. falciparum containing the mutant DHFRs with low cytotoxicity to three mammalian cell lines.
ISSN: 00222623
Appears in Collections:Scopus 2001-2005

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