Synthesis and biological evaluation of natural-product-inspired, aminoalkyl-substituted 1-benzopyrans as novel antiplasmodial agents

Herein, relationships between the structures of 1-aminoethyl-substituted chromenes and their antimalarial activities were thoroughly investigated. At first, the methyl moiety in the side chain was removed to eliminate chirality. The hydrogenation state of the benzopyran system, the position of the p...

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Main Authors: Uth, Jan-Frederik (Author) , Börgel, Frederik (Author) , Lehmkuhl, Kirstin (Author) , Schepmann, Dirk (Author) , Kaiser, Marcel (Author) , Jabor, Valquiria A. P. (Author) , Nonato, Maria Cristina (Author) , Krauth-Siegel, Renate (Author) , Schmidt, Thomas J. (Author) , Wünsch, Bernhard (Author)
Format: Article (Journal)
Language:English
Published: April 26, 2021
In: Journal of medicinal chemistry
Year: 2021, Volume: 64, Issue: 9, Pages: 6397-6409
ISSN:1520-4804
DOI:10.1021/acs.jmedchem.1c00483
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.jmedchem.1c00483
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Author Notes:Jan-Frederik Uth, Frederik Börgel, Kirstin Lehmkuhl, Dirk Schepmann, Marcel Kaiser, Valquiria A.P. Jabor, Maria Cristina Nonato, R. Luise Krauth-Siegel, Thomas J. Schmidt, and Bernhard Wünsch

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520 |a Herein, relationships between the structures of 1-aminoethyl-substituted chromenes and their antimalarial activities were thoroughly investigated. At first, the methyl moiety in the side chain was removed to eliminate chirality. The hydrogenation state of the benzopyran system, the position of the phenolic OH moiety, and the distance of the basic amino moiety toward both aromatic rings were varied systematically. 1-Benzopyran-5-ol 8b (IC50 = 10 nM), 1-benzopyran-7-ol 9c (IC50 = 38 nM), and the aminoalcohol 19c (IC50 = 17 nM) displayed antiplasmodial activity with IC50 values below 50 nM. To identify the mechanism of action, inhibition of three key enzymes by 9c was investigated. 9c was not able to reduce the number of Plasmodia in erythrocytes of mice. This low in vivo activity was explained by fast clearance from blood plasma combined with rapid biotransformation of 9c. Three main metabolites of 9c were identified by liquid chromatography-mass spectrometry (LC-MS) methods. 
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