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Decanoyl-RVKR-CMK was designed to target and inhibit specific proteases with high selectivity and potency. The RVKR sequence is a recognition motif for several proteases, including those involved in coagulation and other physiological processes. By mimicking this sequence, Decanoyl-RVKR-CMK acts as a substrate analog, binding to the active site of target proteases. The chloromethyl ketone group then reacts with a serine or cysteine residue in the active site, forming a covalent bond that irreversibly inactivates the enzyme. In vitro investigations have unveiled the anti-angiogenic properties of Decanoyl-RVKR-CMK, indicating its ability to impede the growth of blood vessels, and it has also exhibited inhibitory effects on the proliferation of cancer cells.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Decanoyl-RVKR-CMK, 500 µg | sc-477835A | 500 µg | $127.00 | |||
Decanoyl-RVKR-CMK, 1 mg | sc-477835 | 1 mg | $234.00 | |||
Decanoyl-RVKR-CMK, 5 mg | sc-477835B | 5 mg | $947.00 |