<i>N</i>‐Substituted Bridged Azaozonides as Promising Antimalarial Agents

Forty-five aminoperoxides belonging to bridged azaozonides, bridged N-substituted azaozonides, and tricyclic aminoperoxides were evaluated for in vitro antimalarial activity against Plasmodium falciparum (3D7) and for cytotoxicity against immortalized human normal liver (LO<sub>2</sub>) and lung (BEAS-2B) cell lines, as well as human liver (HepG2) and lung (A549) cancer cell lines. Seven N-substituted azaozonides exhibited high antimalarial activity against the chloroquine-sensitive 3D7 strain of P. falciparum, with IC<sub>50</sub> < 1 μM. The lead compound 22 showed IC<sub>50</sub> = 0.07 μM and selectivity index of 1428. Most aminoperoxides were generally non-cytotoxic to both normal and cancer liver and lung cells. Only two azaozonides exhibited moderate cytotoxicity on HepG2 cell line (2: IC<sub>50</sub> = 4.12 μM, 40: 9.95 μM), while one azaozonide 2 had an IC<sub>50</sub> = 5.56 μM against A549 cell line. From this small library of 45 aminoperoxides, compound 22 was found to have antimalarial activity comparable to artemisinin and chloroquine used in medical practice. These findings provide a new source for developing antimalarial agents through structural modification of aminoperoxide compounds.

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Publication Details

Journal
ChemMedChem
Published
2025-04-17
DOI
https://doi.org/10.1002/cmdc.202500181
Citations
1
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
1.88

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N‐Substituted Bridged Azaozonides as Promising Antimalarial Agents

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article

N‐Substituted Bridged Azaozonides as Promising Antimalarial Agents

Vincent Kam Wai Wong, Alexander Olegovich Terent'ev, Yulia Yu. Belyakova, Parichat Prommana, Paolo Coghi, Ivan A. Yaremenko, Chairat Uthaipibull, Ali Adnan Nasim, Peter S. Radulov, Ruihong Chen
article en
1 citations

Abstract

Forty-five aminoperoxides belonging to bridged azaozonides, bridged N-substituted azaozonides, and tricyclic aminoperoxides were evaluated for in vitro antimalarial activity against Plasmodium falciparum (3D7) and for cytotoxicity against immortalized human normal liver (LO<sub>2</sub>) and lung (BEAS-2B) cell lines, as well as human liver (HepG2) and lung (A549) cancer cell lines. Seven N-substituted azaozonides exhibited high antimalarial activity against the chloroquine-sensitive 3D7 strain of P. falciparum, with IC<sub>50</sub> < 1 μM. The lead compound 22 showed IC<sub>50</sub> = 0.07 μM and selectivity index of 1428. Most aminoperoxides were generally non-cytotoxic to both normal and cancer liver and lung cells. Only two azaozonides exhibited moderate cytotoxicity on HepG2 cell line (2: IC<sub>50</sub> = 4.12 μM, 40: 9.95 μM), while one azaozonide 2 had an IC<sub>50</sub> = 5.56 μM against A549 cell line. From this small library of 45 aminoperoxides, compound 22 was found to have antimalarial activity comparable to artemisinin and chloroquine used in medical practice. These findings provide a new source for developing antimalarial agents through structural modification of aminoperoxide compounds.

ChemMedChemVol. 20(13)
Macau University of Science and Technology (MO), Russian Academy of Sciences (RU), National Science and Technology Development Agency (TH), Guangdong Medical College (CN), University of Macau (MO), N.D. Zelinsky Institute of Organic Chemistry (RU), National Center for Genetic Engineering and Biotechnology (TH)
National Science and Technology Development Agency, Thailand Research Fund, Fundo para o Desenvolvimento das Ciências e da Tecnologia, National Center for Genetic Engineering and Biotechnology, Macau University of Science and Technology
Good health and well-being
Openalex Percentile: Top 17%
Malaria Research and Control
1.88
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