Melatonin-d4 is a deuterium-labeled derivative of the hormone melatonin, primarily known for activating melatonin receptors. It exhibits antioxidative and anti-inflammatory properties, making it valuable in various biochemical research applications. Additionally, Melatonin-d4 serves as a selective inhibitor of ATF-6, inducing apoptosis in human hepatoma cells through the downregulation of COX-2. This reagent is useful for studying cellular mechanisms related to melatonin and its derivatives in therapeutic contexts.
Melatonin-d4 is a deuterium-labeled derivative of the hormone melatonin, primarily known for activating melatonin receptors. It exhibits antioxidative and anti-inflammatory properties, making it valuable in various biochemical research applications. Additionally, Melatonin-d4 serves as a selective inhibitor of ATF-6, inducing apoptosis in human hepatoma cells through the downregulation of COX-2. This reagent is useful for studying cellular mechanisms related to melatonin and its derivatives in therapeutic contexts.
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