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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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Targets the Bcr-Abl tyrosine kinase, inhibiting its activity. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $272.00 | 18 | |
Estrogen receptor antagonist in breast tissues. | ||||||
Letrozole | 112809-51-5 | sc-204791 sc-204791A | 25 mg 50 mg | $87.00 $147.00 | 5 | |
Aromatase inhibitor blocking the conversion of androgens to estrogens, used in breast cancer therapy. | ||||||
Acarbose | 56180-94-0 | sc-203492 sc-203492A | 1 g 5 g | $226.00 $605.00 | 1 | |
Inhibits alpha-glucosidase, reducing carbohydrate digestion/absorption in the intestines for diabetes care. | ||||||
Allopurinol | 315-30-0 | sc-207272 | 25 g | $131.00 | ||
Inhibits xanthine oxidase, decreasing uric acid production. | ||||||
Atorvastatin | 134523-00-5 | sc-337542A sc-337542 | 50 mg 100 mg | $257.00 $505.00 | 9 | |
Inhibits HMG-CoA reductase, reducing cholesterol synthesis in the liver. Used for cholesterol management. | ||||||
Fluoxetine | 54910-89-3 | sc-279166 | 500 mg | $318.00 | 9 | |
Selective serotonin reuptake inhibitor (SSRI) increasing serotonin concentration in the synaptic cleft. | ||||||
Donepezil | 120014-06-4 | sc-279006 | 10 mg | $74.00 | 3 | |
Inhibits acetylcholinesterase, raising acetylcholine levels, and is used in Alzheimer's | ||||||
Ritonavir | 155213-67-5 | sc-208310 | 10 mg | $124.00 | 7 | |
Protease inhibitor used against HIV. blocks the proteolytic cleavage of virus proteins into functional units. | ||||||
Isoniazid | 54-85-3 | sc-205722 sc-205722A sc-205722B | 5 g 50 g 100 g | $26.00 $101.00 $146.00 | ||
Inhibits the synthesis of mycolic acid in Mycobacterium tuberculosis. | ||||||