Z21090 is a selective inhibitor of phosphodiesterase-4 (PDE4), exhibiting an IC50 value of 37.4 nM and demonstrating oral bioavailability. This compound is significant for studies related to alcohol-related diseases and offers potential therapeutic insights into inflammatory processes and neurodegenerative conditions associated with PDE4 activity. Researchers may utilize Z21090 to explore its effects on cyclic AMP signaling pathways and related biological mechanisms.
Z21090 is a selective inhibitor of phosphodiesterase-4 (PDE4), exhibiting an IC50 value of 37.4 nM and demonstrating oral bioavailability. This compound is significant for studies related to alcohol-related diseases and offers potential therapeutic insights into inflammatory processes and neurodegenerative conditions associated with PDE4 activity. Researchers may utilize Z21090 to explore its effects on cyclic AMP signaling pathways and related biological mechanisms.
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