Cardol triene is a phenolic compound that serves as a competitive and irreversible inhibitor of mushroom tyrosinase, with an IC50 of 22.5 μM. This compound exhibits significant schistosomicidal activity, demonstrating the ability to eliminate 25%, 75%, and 100% of Schistosoma mansoni worms within 24 hours at concentrations of 50, 100, and 200 μM, respectively. Additionally, Cardol triene is utilized as a precursor in the synthesis of bis-benzoxazines, making it a valuable reagent for research in parasitology and synthetic chemistry.
Cardol triene is a phenolic compound that serves as a competitive and irreversible inhibitor of mushroom tyrosinase, with an IC50 of 22.5 μM. This compound exhibits significant schistosomicidal activity, demonstrating the ability to eliminate 25%, 75%, and 100% of Schistosoma mansoni worms within 24 hours at concentrations of 50, 100, and 200 μM, respectively. Additionally, Cardol triene is utilized as a precursor in the synthesis of bis-benzoxazines, making it a valuable reagent for research in parasitology and synthetic chemistry.
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