APC2 inhibitors, also known as Anaphase-Promoting Complex 2 inhibitors, belong to a class of compounds that play a pivotal role in regulating cell cycle progression and maintaining genomic stability. These inhibitors target a key component of the ubiquitin-proteasome system, the Anaphase-Promoting Complex 2 (APC2), which is responsible for orchestrating the degradation of specific proteins at precise points in the cell cycle. The APC2 is a multi-subunit E3 ubiquitin ligase that primarily functions during mitosis and G1 phase to control the orderly progression of the cell cycle. It acts by tagging target proteins with ubiquitin molecules, marking them for degradation by the proteasome, thereby ensuring that cells progress through the cell cycle in a highly regulated manner.
APC2 inhibitors are designed to interfere with the activity of the APC2 complex, preventing it from recognizing and ubiquitinating its target proteins. These compounds typically bind to specific sites on the APC2 protein, disrupting its function and leading to the accumulation of critical cell cycle regulators. The inhibition of APC2 activity can have profound effects on cell cycle regulation, ultimately impacting cell proliferation, differentiation, and cell fate determination. Researchers and scientists studying the cell cycle and related cellular processes often employ APC2 inhibitors as valuable tools in their investigations.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
A peptide aldehyde that can inhibit proteasome function, thereby indirectly affecting APC2's role in protein degradation. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
A boronic acid dipeptide that inhibits the 26S proteasome, potentially increasing the levels of proteins that APC2 would normally target for degradation. | ||||||
Epoxomicin | 134381-21-8 | sc-201298C sc-201298 sc-201298A sc-201298B | 50 µg 100 µg 250 µg 500 µg | $137.00 $219.00 $449.00 $506.00 | 19 | |
A naturally occurring epoxyketone that inhibits proteasome activity, which could indirectly stabilize APC2 substrates. | ||||||
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | $286.00 | 1 | |
A small molecule inhibitor of NEDD8-activating enzyme, affecting neddylation and subsequently the activity of cullin-RING ligases, which may indirectly impact APC2's function. | ||||||
Ubiquitin E1 Inhibitor, PYR-41 | 418805-02-4 | sc-358737 | 25 mg | $360.00 | 4 | |
An irreversible inhibitor of the ubiquitin-activating enzyme E1, potentially disrupting ubiquitin conjugation that APC2 is involved in. | ||||||
IU1 | 314245-33-5 | sc-361215 sc-361215A sc-361215B | 10 mg 50 mg 100 mg | $138.00 $607.00 $866.00 | 2 | |
A small molecule that inhibits USP14, a deubiquitinating enzyme associated with the proteasome, which could modulate the degradation process involving APC2. | ||||||
Lactacystin | 133343-34-7 | sc-3575 sc-3575A | 200 µg 1 mg | $188.00 $575.00 | 60 | |
The active form of lactacystin that irreversibly inhibits proteasome, influencing APC2's ability to target proteins for degradation. | ||||||
Carfilzomib | 868540-17-4 | sc-396755 | 5 mg | $41.00 | ||
An epoxyketone proteasome inhibitor that irreversibly binds to and inhibits the proteasome, potentially affecting APC2's substrate turnover. | ||||||
Oprozomib | 935888-69-0 | sc-477447 | 2.5 mg | $280.00 | ||
An oral proteasome inhibitor that could indirectly affect APC2's role in the cell cycle by inhibiting proteolysis of its substrates. | ||||||