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Ikekawa et al. (1982) demonstrated that proflamin inhibited the growth of Sarcoma 180 in mice with tumor inhibition rates exceeding 80%. Further work showed that the antitumor effect was host-mediated, as proflamin was inactive against tumor cells in vitro but highly effective in immunocompetent animals. Macrophage activation and NK cell enhancement were confirmed as primary mechanisms. Evidence is preclinical.
Representative pattern: C₄H₂NO
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