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 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Paroxetine HCl

78246-49-8sc-201141
sc-201141A
20 mg
100 mg
$117.00
$445.00
2
(1)

Paroxetine HCl (CAS 78246-49-8) is a chemical compound known to function as an inhibitor of CYP2D6. It can interact with the active site of CYP2D6.

Mepyramine maleate

59-33-6sc-203629
sc-203629A
100 mg
1 g
$65.00
$220.00
1
(1)

Mepyramine maleate (CAS 59-33-6) is a chemical compound that acts as an inhibitor of the enzyme CYP2D6.

Paroxetine

61869-08-7sc-507527
1 g
$180.00
(0)

Paroxetine inhibits CYP2D6 through a mechanism that involves direct binding to the enzyme's active site, acting as a competitive inhibitor. This interaction prevents the access of substrates to the catalytic center of CYP2D6, thereby reducing the enzyme's ability to metabolize these compounds.

α-Asarone

2883-98-9sc-239153
1 g
$56.00
(0)

α-Asarone (CAS 2883-98-9) is a chemical compound known for its role as an inhibitor of the enzyme CYP2D6.

Fluoxetine

54910-89-3sc-279166
500 mg
$312.00
9
(1)

Fluoxetine inhibits CYP2D6 by directly binding to the enzyme's active site in a competitive manner. This binding effectively blocks substrate access to the catalytic site of CYP2D6, diminishing the enzyme's metabolic activity.

Mirabegron

223673-61-8sc-211912
500 mg
$357.00
5
(3)

Mirabegron (CAS 223673-61-8) is a chemical compound known for its inhibitory effects on the enzyme CYP2D6.

Duloxetine Hydrochloride

136434-34-9sc-207599
sc-207599A
sc-207599B
10 mg
100 mg
1 g
$195.00
$311.00
$658.00
1
(1)

Duloxetine Hydrochloride inhibits CYP2D6 by competitively binding to the active site of the enzyme. This action blocks the access of CYP2D6′s natural substrates to the enzyme′s catalytic site, thereby inhibiting its metabolic function.

Quinidine

56-54-2sc-212614
10 g
$102.00
3
(1)

Quinidine is a potent competitive inhibitor of CYP2D6, binding with high affinity to the enzyme's active site. This binding effectively blocks the access of substrates to the enzyme, significantly reducing CYP2D6's ability to metabolize these compounds.

Fluvoxamine

54739-18-3sc-207697
25 mg
$315.00
1
(0)

Fluvoxamine acts as a competitive inhibitor of CYP2D6, directly interacting with the enzyme's active site. This prevents the binding and metabolism of CYP2D6 substrates, leading to a decrease in enzyme activity.

Amiodarone

1951-25-3sc-480089
5 g
$312.00
(1)

Amiodarone inhibits CYP2D6 potentially through both competitive and allosteric mechanisms. By binding to the active site and possibly altering the enzyme's conformation, Amiodarone reduces the efficiency of substrate metabolism.