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N-Heptylformamide is a small molecule that functions as a potent and selective inhibitor of various alcohol dehydrogenase (ADH) isoenzymes. It has been shown to inhibit human ADH4, HsADH sigma, and HsADH beta1. This compound has been utilized in research to investigate the metabolism of 20-hydroxyeicosatetraenoic acid (20-HETE) in cerebral microvessels, where it decreased the conversion of 20-HETE to 20-carboxyeicosatetraenoic acid (20-COOH-AA) by inhibiting ADH4. Additionally, N-Heptylformamide has been employed in structural studies to understand the binding characteristics and substrate preferences of different ADH isoenzymes.
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