Phenacetin-d5 is a deuterium-labeled derivative of Phenacetin, functioning primarily as a stable isotope. As a non-opioid analgesic and antipyretic agent, Phenacetin selectively inhibits COX-3. This compound serves as a valuable probe for studying cytochrome P450 enzymes, particularly CYP1A2, in human liver microsomes and rat models, facilitating research in drug metabolism and pharmacokinetics.
Phenacetin-d5 is a deuterium-labeled derivative of Phenacetin, functioning primarily as a stable isotope. As a non-opioid analgesic and antipyretic agent, Phenacetin selectively inhibits COX-3. This compound serves as a valuable probe for studying cytochrome P450 enzymes, particularly CYP1A2, in human liver microsomes and rat models, facilitating research in drug metabolism and pharmacokinetics.
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