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All targets

Molecular target

Heme-Iron Radical / Endoperoxide Alkylation

Also: artemisinin activation · id HEME_IRON_RADICAL

Heme-iron–mediated free-radical mechanism: parasite ferrous iron cleaves the artemisinin endoperoxide bridge, generating carbon-centered radicals that alkylate heme and parasite proteins. The artemisinin antimalarial mechanism — distinct from heme-polymerization (hemozoin) inhibition by quinoline antimalarials such as chloroquine and quinine.

1 drug act here1 plant reach it via their compounds

Educational use only. This page summarizes published research and traditional-use records for educational purposes. It does not diagnose, treat, cure, or prevent any disease. Do not start, stop, or change medications based on this information. Discuss any decisions about therapies — pharmaceutical or botanical — with a qualified clinician who knows your medical history.

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Pharmaceutical agents

Drugs that act on Heme-Iron Radical / Endoperoxide Alkylation

These medications have Heme-Iron Radical / Endoperoxide Alkylation among their molecular targets. Sharing a target is a mechanistic relationship — it does not make any plant below an alternative to, or substitute for, these drugs.

Botanical connections

Plants whose compounds act on Heme-Iron Radical / Endoperoxide Alkylation

Each plant below contains a named compound documented to act on Heme-Iron Radical / Endoperoxide Alkylation. The compound and the reason for the connection are shown on every edge — a shared mechanism, not a therapeutic equivalence.

  • ArtemisininSesquiterpene endoperoxide lactone

    Artemisinin’s endoperoxide bridge is cleaved by heme/ferrous iron to generate carbon-centered radicals that alkylate heme and parasite proteins — the antimalarial mechanism shared with its semi-synthetic derivative artemether.

A shared molecular target shows how a botanical and a drug relate mechanistically. It is not evidence that one can replace the other. Educational summary only — discuss any medication decision with your clinician.