Crocacin A is an anti-fungal agent that demonstrates inhibitory effects against yeast and filamentous fungi. Additionally, it has the capacity to inhibit the proliferation of mouse fibroblast cell line L929. Mechanistically, Crocacin A disrupts the bc1 complex of the electron transport chain in calf heart microsomes, resulting in a noticeable redshift in the 569 nm peak of the cytochrome B reduction spectrum. This compound is useful for researching fungal infections and exploring mitochondrial function and pathology.
Crocacin A is an anti-fungal agent that demonstrates inhibitory effects against yeast and filamentous fungi. Additionally, it has the capacity to inhibit the proliferation of mouse fibroblast cell line L929. Mechanistically, Crocacin A disrupts the bc1 complex of the electron transport chain in calf heart microsomes, resulting in a noticeable redshift in the 569 nm peak of the cytochrome B reduction spectrum. This compound is useful for researching fungal infections and exploring mitochondrial function and pathology.
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