Our examination of inhibitor or substrate profiles of compounds 2 – 10 and carprofen included highly significant cytochromes in medication metabolization, namely CYP2D6, CYP3A4, CYP1A2, CYP2C19, and CYP2C9, reflecting the pharmacogenomic profile of the compounds ( Table 6 ).
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In Silico and Experimental Investigation of the Biological Potential of Some Recently Developed Carprofen Derivatives.
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