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It was originally developed by researchers at Monash University in Australia in the 1990s as a potential anti-obesity drug

Among them, enhanced metabolic detoxification and target site insensitivity are the most common mechanisms [5, 33-35]

Contrastingly, there was one participant who was a low GR converter when provided with endogenous myrosinase and slightly better when given GR alone, and one participant who converted 13%) product that is shelf stable at room temperature and well-suited for inclusion in a variety of commercial food and supplement formats including drinks, capsules and tablets