Date published: 2026-4-1

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EXD Inhibitors

EXD inhibitors, short for Epoxide Hydrolase and Xenobiotic Diol Epoxide Hydrolase inhibitors, constitute a class of chemical compounds primarily recognized for their role in modulating enzymatic activities within the cytochrome P450 superfamily. These enzymes play a pivotal role in the detoxification and metabolism of xenobiotics, including environmental toxins. The inhibition of Epoxide Hydrolases and Xenobiotic Diol Epoxide Hydrolases, abbreviated as EH and XEH, respectively, is of particular interest in the context of pharmacology and toxicology, as it can influence the bioavailability and elimination rates of various foreign compounds within the body.

Chemically, EXD inhibitors encompass a diverse array of small molecules that share a common feature: the ability to interact with the active sites of EH and XEH enzymes, thereby impeding their catalytic functions. These inhibitors often contain functional groups that mimic the substrates of these enzymes, allowing them to competitively bind to the active sites and obstruct the enzymatic hydrolysis of epoxides and diol epoxides. As a result, EXD inhibitors can alter the metabolic pathways of xenobiotics, leading to the accumulation of toxic intermediates or the formation of more soluble metabolites that are easier to eliminate. This class of compounds is instrumental in understanding the intricate mechanisms of xenobiotic metabolism and has broad implications in drug development, environmental toxicology, and the study of chemical carcinogenesis. Researchers continue to explore the diverse chemical structures and pharmacological properties of EXD inhibitors, aiming to uncover their broader roles in xenobiotic metabolism and related biochemical processes.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$26.00
$119.00
$213.00
27
(1)

Targets the Bcr-Abl tyrosine kinase, inhibiting its activity.

Tamoxifen

10540-29-1sc-208414
2.5 g
$272.00
18
(2)

Estrogen receptor antagonist in breast tissues.

Letrozole

112809-51-5sc-204791
sc-204791A
25 mg
50 mg
$87.00
$147.00
5
(1)

Aromatase inhibitor blocking the conversion of androgens to estrogens, used in breast cancer therapy.

Acarbose

56180-94-0sc-203492
sc-203492A
1 g
5 g
$226.00
$605.00
1
(1)

Inhibits alpha-glucosidase, reducing carbohydrate digestion/absorption in the intestines for diabetes care.

Allopurinol

315-30-0sc-207272
25 g
$131.00
(0)

Inhibits xanthine oxidase, decreasing uric acid production.

Atorvastatin

134523-00-5sc-337542A
sc-337542
50 mg
100 mg
$257.00
$505.00
9
(1)

Inhibits HMG-CoA reductase, reducing cholesterol synthesis in the liver. Used for cholesterol management.

Fluoxetine

54910-89-3sc-279166
500 mg
$318.00
9
(1)

Selective serotonin reuptake inhibitor (SSRI) increasing serotonin concentration in the synaptic cleft.

Donepezil

120014-06-4sc-279006
10 mg
$74.00
3
(1)

Inhibits acetylcholinesterase, raising acetylcholine levels, and is used in Alzheimer's

Ritonavir

155213-67-5sc-208310
10 mg
$124.00
7
(1)

Protease inhibitor used against HIV. blocks the proteolytic cleavage of virus proteins into functional units.

Isoniazid

54-85-3sc-205722
sc-205722A
sc-205722B
5 g
50 g
100 g
$26.00
$101.00
$146.00
(1)

Inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis.