Please use this identifier to cite or link to this item: https://doi.org/10.1021/jm0101747
Title: Antimalarial alkoxylated and hydroxylated chalones: Structure-activity relationship analysis
Authors: Liu, M.
Wilairat, P.
Go, M.-L. 
Issue Date: 6-Dec-2001
Citation: Liu, M., Wilairat, P., Go, M.-L. (2001-12-06). Antimalarial alkoxylated and hydroxylated chalones: Structure-activity relationship analysis. Journal of Medicinal Chemistry 44 (25) : 4443-4452. ScholarBank@NUS Repository. https://doi.org/10.1021/jm0101747
Abstract: Chalcones with 2′,3′,4′-trimethoxy, 2′,4′-dimethoxy, 4′-methoxy, 4′-ethoxy, 2′,4′-dihydroxy, and 4′-hydroxy groups on ring B were synthesized and evaluated in vitro against Plasmodium falciparum (K1) in a [3H] hypoxanthine uptake assay. The other ring A was quinoline, pyridine, naphthalene, or phenyl rings with electron-donating or electron-withdrawing substituents of varying lipophilicities. Trimethoxy 6 and 27, dimethoxy 7, 8, 29, and methoxy 31 analogues had good in vitro activities (IC50 < 5μM). 3-Quinolinyl ring A derivatives were well represented among the active compounds. Hydroxylated chalcones were less active than the corresponding alkoxylated analogues. When evaluated in vivo, 8 and 208 were comparable to chloroquine in extending the lifespan of infected mice. Multivariate data analysis showed that in vitro activity was mainly determined by the properties of ring B. Quantitative structure - activity relationship models with satisfactory predictive ability were obtained for various B ring chalcones using projections to latent structures. A model with good predictability was proposed for 19 active chalcones. Size and hydrophobicity were identified as critical parameters.
Source Title: Journal of Medicinal Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/105654
ISSN: 00222623
DOI: 10.1021/jm0101747
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