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Conclusions Artemisinin and its derivatives exhibit more potent antimalarial activity than iron chelators, likely stemming from their ability to accumulate in the parasites digestive vacuoles, interact more effectively with heme and iron, and thereby disrupt heme/iron homeostasis and utilization

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XL184 is useful at low concentration (0.10.5 M) to induce marked inhibition of constitutive and inducible c-Met phosphorylation and its consecutive downstream signaling in malignant peripheral nerve sheath tumor cells