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- W2896614752 abstract "Artemisinin–estrogen hybrids were for the first time both synthesized and investigated for their in vitro biological activity against malaria parasites (Plasmodium falciparum 3D7), human cytomegalovirus (HCMV), and a panel of human malignant cells of gynecological origin containing breast (MCF7, MDA-MB-231, MDA-MB-361, T47D) and cervical tumor cell lines (HeLa, SiHa, C33A). In terms of antimalarial efficacy, hybrid 8 (EC50 = 3.8 nM) was about two times more active than its parent compound artesunic acid (7) (EC50 = 8.9 nM) as well as the standard drug chloroquine (EC50 = 9.8 nM) and was, therefore, comparable to the clinically used dihydroartemisinin (6) (EC50 = 2.4 nM). Furthermore, hybrids 9–12 showed a strong antiviral effect with EC50 values in the submicromolar range (0.22–0.38 μM) and thus possess profoundly stronger anti-HCMV activity (approximately factor 25) than the parent compound artesunic acid (7) (EC50 = 5.41 μM). These compounds also exerted a higher in vitro anti-HCMV efficacy than ganciclovir used as the standard of current antiviral treatment. In addition, hybrids 8–12 elicited substantially more pronounced growth inhibiting action on all cancer cell lines than their parent compounds and the reference drug cisplatin. The most potent agent, hybrid 12, exhibited submicromolar EC50 values (0.15–0.93 μM) against breast cancer and C33A cell lines." @default.
- W2896614752 created "2018-10-26" @default.
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- W2896614752 date "2018-10-19" @default.
- W2896614752 modified "2023-10-16" @default.
- W2896614752 title "Synthesis of Artemisinin–Estrogen Hybrids Highly Active against HCMV, <i>P. falciparum</i>, and Cervical and Breast Cancer" @default.
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- W2896614752 doi "https://doi.org/10.1021/acsmedchemlett.8b00381" @default.
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