APC10 inhibitors are a class of chemical compounds that specifically target and inhibit the function of APC10, a core subunit of the anaphase-promoting complex/cyclosome (APC/C), a multi-subunit E3 ubiquitin ligase complex. APC10 plays a crucial role in recognizing and binding substrates that need to be ubiquitinated for degradation during the cell cycle, particularly in the transition from metaphase to anaphase. This process is essential for proper progression through the cell cycle, as APC/C mediates the ubiquitination and subsequent degradation of key regulatory proteins, such as cyclins and securins, ensuring that cell division occurs in a controlled and orderly manner. APC10 inhibitors interfere with this recognition and binding process, thereby affecting the function of the APC/C complex.
Chemically, APC10 inhibitors are designed to block the interaction between APC10 and its substrate-binding partners or disrupt its role in the overall function of the APC/C complex. These inhibitors may bind directly to APC10's substrate recognition site, preventing the attachment of proteins targeted for ubiquitination, or they may alter the conformation of APC10, rendering it incapable of performing its normal role in substrate processing. The development of APC10 inhibitors often involves structure-based drug design, molecular docking studies, and structure-activity relationship (SAR) analysis to identify compounds with high specificity and potency. By inhibiting APC10, researchers can study the intricate mechanisms governing the cell cycle and the regulatory processes involved in protein degradation through the ubiquitin-proteasome system. These inhibitors provide valuable tools for exploring the dynamic role of APC10 in cellular proliferation, division, and the maintenance of genomic stability.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
A proteasome inhibitor that prevents the degradation of ubiquitinated proteins, affecting APC/C function. | ||||||
Carfilzomib | 868540-17-4 | sc-396755 | 5 mg | $40.00 | ||
An irreversible proteasome inhibitor that could impede the proteolysis mediated by the APC/C. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
A reversible proteasome inhibitor that can also inhibit the degradation of APC/C targets. | ||||||
Lactacystin | 133343-34-7 | sc-3575 sc-3575A | 200 µg 1 mg | $165.00 $575.00 | 60 | |
Specifically inhibits the proteasome, thereby potentially accumulating APC/C substrates. | ||||||
Ubiquitin E1 Inhibitor, PYR-41 | 418805-02-4 | sc-358737 | 25 mg | $360.00 | 4 | |
An inhibitor of the ubiquitin-activating enzyme E1, indirectly affecting ubiquitination processes of APC/C. | ||||||
Cdc2-Like Kinase Inhibitor, TG003 | 300801-52-9 | sc-202528 sc-202528A | 5 mg 25 mg | $136.00 $537.00 | 6 | |
An inhibitor of the APC/C activator proteins, thus indirectly affecting APC/C activity. | ||||||
Withaferin A | 5119-48-2 | sc-200381 sc-200381A sc-200381B sc-200381C | 1 mg 10 mg 100 mg 1 g | $127.00 $572.00 $4090.00 $20104.00 | 20 | |
A steroidal lactone that disrupts proteasomal function, which might lead to an accumulation of APC/C substrates. | ||||||