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Antimalarial Activity of C-10 Substituted Triazolyl Artemisinin
The Korean Journal of Parasitology ; : 661-665, 2017.
Article in English | WPRIM | ID: wpr-58758
ABSTRACT
We synthesized C-10 substituted triazolyl artemisinins by the Huisgen cycloaddition reaction between dihydroartemisinins (2) and variously substituted 1, 2, 3-triazoles (8a-8h). The antimalarial activities of 32 novel artemisinin derivatives were screened against a chloroquine-resistant parasite. Among them, triazolyl artemisinins with electron-withdrawing groups showed stronger antimalarial activities than those shown by the derivatives having electron-donating groups. In particularly, m-chlorotriazolyl artemisinin (9d-12d) showed antimalarial activity equivalent to that of artemisinin and could be a strong drug candidate.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parasites / Artemisinins / Cycloaddition Reaction Language: English Journal: The Korean Journal of Parasitology Year: 2017 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Parasites / Artemisinins / Cycloaddition Reaction Language: English Journal: The Korean Journal of Parasitology Year: 2017 Type: Article