Beauvericin A is a cyclodepsipeptide with potent antibacterial activity, primarily targeting Mycobacterium tuberculosis and Plasmodium falciparum. It exhibits a minimum inhibitory concentration (MIC) of 25 μg/mL against M. tuberculosis and an IC50 of 12 μg/mL against P. falciparum, demonstrating its potential as a valuable agent in infectious disease research. Additionally, Beauvericin A shows toxicity to brine shrimp, indicating its bioactive properties that can be explored in various biological assays.
Beauvericin A is a cyclodepsipeptide with potent antibacterial activity, primarily targeting Mycobacterium tuberculosis and Plasmodium falciparum. It exhibits a minimum inhibitory concentration (MIC) of 25 μg/mL against M. tuberculosis and an IC50 of 12 μg/mL against P. falciparum, demonstrating its potential as a valuable agent in infectious disease research. Additionally, Beauvericin A shows toxicity to brine shrimp, indicating its bioactive properties that can be explored in various biological assays.
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