SIAH-1 inhibitors constitute a distinct class of compounds renowned for their specific interaction with the SIAH-1 protein. As a member of the SIAH family of E3 ubiquitin ligases, SIAH-1 plays a vital role in governing protein degradation through the ubiquitin-proteasome system. These inhibitors stand out due to their precise binding to SIAH-1's active site, disrupting its enzymatic function responsible for transferring ubiquitin molecules onto target proteins. Structurally, SIAH-1 inhibitors feature unique chemical motifs that enable them to fit snugly into the active site of the protein. This interaction interferes with SIAH-1's ubiquitin ligase activity, leading to the stabilization of proteins that would otherwise undergo degradation. The advent of SIAH-1 inhibitors has provided researchers with a powerful tool to dissect intricate protein degradation pathways, shedding light on cellular functions.
Beyond their significance in cellular processes, SIAH-1 inhibitors hold implications. The diverse range of cellular processes influenced by these inhibitors underscores their role in unraveling unexplored facets of biology. As research progresses, the cumulative knowledge about SIAH-1 inhibitors could lead to innovative approaches for addressing various biological challenges.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
SAR405 | 1523406-39-4 | sc-507416 | 1 mg | $125.00 | ||
Identified through high-throughput screening, SAR-405 selectively inhibits SIAH-It stabilizes proteins targeted for degradation by SIAH-1, potentially affecting cancer cell survival pathways. | ||||||
R406 | 841290-81-1 | sc-364595 sc-364595A | 2 mg 10 mg | $160.00 $370.00 | 16 | |
This small molecule inhibitor is designed to target SIAH-In research studies, R406 prevents the degradation of SIAH-1 substrates involved in apoptosis and cellular proliferation. | ||||||
NSC 87877 | 56990-57-9 | sc-204139 | 50 mg | $134.00 | 12 | |
Identified as an SIAH-1 inhibitor, NSC-763862 disrupts its interaction with specific target proteins. This compound has shown potential in inducing apoptosis in cancer cells. | ||||||