Synthesis and in vitro testing of antimalarial activity of non-natural-type neocryptolepines: structureactivity relationship study of 2,11- and 9,11-disubstituted 6-methylindolo[2,3-b]quinolines.
Chem Pharm Bull (Tokyo)
; 61(12): 1282-90, 2013.
Article
em En
| MEDLINE
| ID: mdl-24436959
ABSTRACT
This report describes the synthesis and in vitro anti-malarial evaluations of certain C2 or C8 and C11-disubstituted 6-methyl-5H-indolo[2,3-b]quinoline (neocryptolepine congener) derivatives. To attain higher activities, the structureactivity relationship (SAR) studies were conducted by varying the kind of alkylamino or ω-aminoalkylamino stubstituents at C11 and with Cl at the C2 position, or CO2Me at the C9 position. The anti-malarial activities of the tested compounds were significantly increased compared to the 11-non(alkylamino) derivatives. The 3-aminopropylamino group at C11 was further modified to urea and thiourea, which improved the cytotoxicity against normal cells. The best results were achieved with compounds 8 and 9d against the NF54 strain with the IC(50)/SI values as of 86 nM/20 and 317 nM/370, respectively. Furthermore, the compounds were tested for ß-haematin inhibition. Twelve were found to have IC(50) values below 100 µM and a linear correlation between the ß-haematin inhibition and cell growth inhibition in the NF54 strain was found for those derivatives with basic amino side chains. A second correlation was identified between the NF54 activity and physico-chemical factors related to solvation and polarity.
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Base de dados:
MEDLINE
Assunto principal:
Plasmodium falciparum
/
Quinolinas
/
Alcaloides
/
Indóis
/
Antimaláricos
Tipo de estudo:
Prognostic_studies
Limite:
Animals
/
Humans
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article