Tenidap-d3 is a deuterated form of Tenidap, a non-steroidal anti-inflammatory drug that selectively inhibits COX-1 with an IC50 of 0.03 μM, while showing weaker inhibition of COX-2 at 1.2 μM. This compound exhibits notable anti-inflammatory and antirheumatic effects, making it a valuable reagent in studies of inflammatory pathways. Additionally, Tenidap is identified as a specific inhibitor of SLC26A3, facilitating research into its role in ion transport and related physiological processes.
Tenidap-d3 is a deuterated form of Tenidap, a non-steroidal anti-inflammatory drug that selectively inhibits COX-1 with an IC50 of 0.03 μM, while showing weaker inhibition of COX-2 at 1.2 μM. This compound exhibits notable anti-inflammatory and antirheumatic effects, making it a valuable reagent in studies of inflammatory pathways. Additionally, Tenidap is identified as a specific inhibitor of SLC26A3, facilitating research into its role in ion transport and related physiological processes.
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