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The page below is a sample from the LabCE course Drug Metabolism. Access the complete course and earn ASCLS P.A.C.E.-approved continuing education credits by subscribing online.

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Cytochrome P450 (CYP Enzymes), continued

The CYP enzymes involved in drug metabolism are:
  • CYP3A4 (approximately 40-50%)
  • CYP2D6 (approximately 20-30%)
  • CYP1A2
  • CYP2C9
  • CYP2C19
  • CYP2E1
  • CYP2B6
  • CYP2A6
The following equation illustrates how CYP enzymes facilitate the addition of oxygen to a lipophilic drug to make it more polar and, thus, water soluble:
One atom of oxygen is inserted into the substrate (the drug). The other oxygen atom is reduced to water. The original substrate is now rendered more polar and thus water soluble. If the metabolites are polar enough, they can be excreted. However, most products undergo another reaction which will be discussed later.
Most drugs are deactivated by CYP enzymes, but some are bio-activated to form active metabolites. An example is the conversion of codeine to morphine.