Date published: 2025-10-4

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CYP2D6 Inhibitors

Cytochrome P450 2D6 (CYP2D6) is an enzyme that plays a pivotal role in the metabolism of a wide array of substrates, including numerous endogenous compounds and xenobiotics. This enzyme is a member of the cytochrome P450 superfamily, a group of enzymes critical for the oxidative metabolism of various substances. CYP2D6 is highly expressed in the liver, where it catalyzes the introduction of an oxygen atom into its substrates in a process known as oxidative biotransformation. This action often results in the conversion of lipophilic compounds into more hydrophilic metabolites, facilitating their excretion from the body. The enzyme's activity varies significantly among individuals due to genetic polymorphisms, leading to a wide range of metabolic capacities. The substrates of CYP2D6 include not only pharmaceutical compounds but also endogenous substances, indicating its crucial role in both pharmacology and physiology. By altering the chemical structure of its substrates, CYP2D6 directly influences their pharmacokinetics and dynamics, affecting their biological activity and distribution within the organism. Inhibition of CYP2D6 involves mechanisms that decrease the enzyme's metabolic activity, affecting the clearance and bioavailability of its substrates. Inhibitors of CYP2D6 can act through various mechanisms, including competitive, non-competitive, and uncompetitive inhibition. Competitive inhibitors bind to the active site of the enzyme, directly competing with the substrate for binding, thereby reducing the rate of substrate metabolism. Non-competitive inhibitors, on the other hand, bind to an allosteric site on the enzyme, altering its conformation in a way that diminishes its catalytic efficiency without affecting substrate binding. Uncompetitive inhibitors typically bind to the enzyme-substrate complex, further preventing the catalytic activity of the enzyme. These inhibitory actions can lead to an accumulation of substrates, altering their expected metabolic processing and potentially affecting the metabolic pathways in which CYP2D6 is involved. Moreover, the inhibition of CYP2D6 can have a significant impact on the metabolic clearance of its substrates, leading to alterations in their concentration in the body.

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Items 11 to 12 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Escitalopram

128196-01-0sc-357349
sc-357349A
10 mg
50 mg
$128.00
$408.00
2
(0)

Escitalopram exhibits mild competitive inhibition of CYP2D6, binding to the enzyme's active site and reducing substrate metabolism. This interaction, while less potent than some other inhibitors, still leads to a decrease in CYP2D6 activity.

Reduced Haloperidol

34104-67-1sc-212770
25 mg
$300.00
(1)

Reduced Haloperidol (CAS 34104-67-1) is a chemical compound known for its inhibitory properties against the enzyme CYP2D6. Reduced Haloperidol's inhibitory activity on CYP2D6 can potentially impact the pharmacokinetics of certain substances.