Neprilysin-2 inhibitors, also known as NEP2 inhibitors, belong to a specific chemical class of compounds designed to target and inhibit the enzymatic activity of neprilysin-2 (NEP2), which is a member of the metalloprotease family of enzymes. These inhibitors are primarily characterized by their ability to selectively bind to the active site of NEP2, thereby impeding its catalytic function. Neprilysin-2, like its closely related counterpart neprilysin (NEP), plays a pivotal role in the degradation of various endogenous peptides, particularly those involved in regulating physiological processes such as blood pressure, inflammation, and tissue remodeling.
Neprilysin-2 inhibitors often feature specific pharmacophoric moieties that interact with the active site residues of NEP2, effectively blocking its proteolytic activity. These inhibitors can be developed using a variety of chemical scaffolds, including small organic molecules or peptidomimetics, and are characterized by their selectivity for NEP2 over other enzymes in the metalloprotease family. By inhibiting NEP2, these compounds may have the potential to modulate the levels of various bioactive peptides in the body, which could have implications in the context of research related to understanding the physiological roles of these peptides and their involvement in disease processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phosphoramidon | 119942-99-3 | sc-201283 sc-201283A | 5 mg 25 mg | $199.00 $632.00 | 8 | |
Phosphoramidon is a reversible NEP inhibitor that chelates the zinc ion at the active site, preventing the hydrolysis of peptide substrates. | ||||||
Candoxatril | 123122-55-4 | sc-504600 | 10 mg | $13500.00 | ||
Candoxatril is a prodrug that, once hydrolyzed to candoxatrilat, inhibits NEP by interacting with the active site to block substrate access. | ||||||
Sialorphin | 131748-26-0 | sc-253554 | 1 mg | $237.00 | ||
Sialorphin is a natural inhibitor of NEP, which acts by binding to the enzyme's active site and preventing the breakdown of enkephalins, natural substrates of NEP. | ||||||
SM-19712 | 194542-56-8 | sc-215859 sc-215859A | 5 mg 25 mg | $235.00 $869.00 | ||
SM-19712 is a selective NEP inhibitor that binds to the zinc-containing active site, inhibiting the enzyme's ability to cleave peptides. | ||||||
UK 383367 | 348622-88-8 | sc-361393 sc-361393A | 5 mg 25 mg | $115.00 $434.00 | 1 | |
UK-383367 is a potent inhibitor of NEP, which binds to the active site and inhibits the enzyme's peptidase activity. | ||||||