KTELC1 inhibitors represent a class of chemical compounds that specifically target and interact with the KTELC1 protein, modulating its activity within cellular processes. KTELC1, which stands for Kinetochore-Localized E3 Ligase Complex 1, is a critical component of the cellular machinery responsible for accurate chromosome segregation during cell division, a process known as mitosis. This protein complex plays a pivotal role in ensuring that each daughter cell receives the correct number of chromosomes, inhibiting genetic instability and aneuploidy, which can lead to various diseases, including cancer. KTELC1 inhibitors have garnered significant attention in the field of cell biology and drug discovery due to their potential to interfere with this essential biological process.
Structurally, KTELC1 inhibitors are diverse compounds designed to disrupt the normal function of the KTELC1 protein complex. These inhibitors may bind to specific sites on KTELC1, inhibiting its enzymatic activity or blocking its interaction with other crucial cellular components involved in the mitotic process. By interfering with KTELC1, these compounds have the potential to disrupt mitosis and halt the cell cycle, which can be of interest in both basic research and potential drug development efforts. The study of KTELC1 inhibitors not only deepens our understanding of the intricacies of cell division but also opens up new avenues for exploring their roles in cellular biology and their potential applications.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
JIB 04 | 199596-05-9 | sc-397040 | 20 mg | $177.00 | ||
JIB-04 is a pan-KDM inhibitor. It selectively inhibits the demethylase activity of KDMs, thereby modulating gene expression. | ||||||
GSK-J4 | 1373423-53-0 | sc-507551 | 100 mg | $1275.00 | ||
GSK-J4 is a selective inhibitor for the KDM6 family, but also has activity against KDM4C/D. It affects H3K27 demethylation, leading to changes in gene expression. | ||||||
A-366 | 1527503-11-2 | sc-507495 | 10 mg | $195.00 | ||
A-366 is a selective inhibitor of KDM5 proteins. It selectively blocks KDM5 demethylation, affecting gene transcription. | ||||||
Chidamide | 743420-02-2 | sc-364462 sc-364462A sc-364462B | 1 mg 5 mg 25 mg | $61.00 $245.00 $1173.00 | ||
While primarily a HDAC inhibitor, it also has activity against certain KDMs, affecting histone acetylation and methylation. | ||||||