Isopedicin is a potent phosphodiesterase (PDE) inhibitor that effectively reduces superoxide anion (O2•-) production in formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP)-activated cells. By inhibiting PDE activity, Isopedicin enhances cyclic AMP (cAMP) formation and promotes protein kinase A (PKA) activity, thereby influencing various intracellular signaling pathways. This compound is suitable for research applications investigating oxidative stress and signaling mechanisms in immune responses.
Isopedicin is a potent phosphodiesterase (PDE) inhibitor that effectively reduces superoxide anion (O2•-) production in formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP)-activated cells. By inhibiting PDE activity, Isopedicin enhances cyclic AMP (cAMP) formation and promotes protein kinase A (PKA) activity, thereby influencing various intracellular signaling pathways. This compound is suitable for research applications investigating oxidative stress and signaling mechanisms in immune responses.
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