(S)-6-amino-2-((S)-2-((S)-2-((S)-2-amino-3-carboxypropanamido)propanamido)-3-(1H-imidazol-4-yl)propanamido)hexanoic acid
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DAHK inhibits Cu(II)-induced oxidative DNA double strand breaks. The tetrapeptide is as effective as HSA in preventing neuronal death induced by CuCl2/ascorbic acid. It may be an effective, small-molecular-weight alternative to HSA as a therapeutic agent for stroke.
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