Synthesis and in Vitro Testing of Antimalarial Activity of Non-natural-Type Neocryptolepines: Structure–Activity Relationship Study of 2,11- and 9,11-Disubstituted 6-Methylindolo[2,3-b]quinolines
| Autor: | Ryuhei Misumi, Kathryn J. Wicht, Tsutomu Inokuchi, Ibrahim El Tantawy El Sayed, Ahmed A. El Gokha, Ming-qi Wang, Wen-Jie Lu, Ning Wang, Marcel Kaiser, Li Wang, Timothy J. Egan |
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| Rok vydání: | 2013 |
| Předmět: | |
| Zdroj: | Chemical and Pharmaceutical Bulletin. 61:1282-1290 |
| ISSN: | 1347-5223 0009-2363 |
| DOI: | 10.1248/cpb.c13-00639 |
| Popis: | 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 structure–activity 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 β-haematin inhibition. Twelve were found to have IC(50) values below 100 µM and a linear correlation between the β-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. |
| Databáze: | OpenAIRE |
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