Reaper inhibitors represent a class of chemical compounds that have been identified to counteract the activity of the reaper protein, predominantly characterized in the fruit fly, Drosophila melanogaster. The reaper protein is a pivotal component of the apoptotic pathway in these organisms, serving as a regulator and initiator of programmed cell death. Its primary mechanism of action involves the antagonism of Inhibitor of Apoptosis Proteins (IAPs), which, in their normal state, inhibit the activation of caspases, the primary executioners of apoptosis. By inhibiting IAPs, reaper facilitates the activation of these caspases, leading to cellular apoptosis. Hence, any chemical compound that can neutralize the effects of reaper would essentially be inhibiting a crucial pro-apoptotic trigger within the cell.
The study of reaper inhibitors, therefore, largely revolves around understanding the intricate balance of pro- and anti-apoptotic signals within a cell. A majority of these inhibitors are designed to target specific biochemical interactions, such as the binding of reaper to IAPs. By impeding this binding, these inhibitors can maintain the inactivity of caspases, ensuring cell survival. Additionally, other reaper inhibitors might function by enhancing the activity or expression of IAPs, indirectly counteracting reaper's effects. It's also noteworthy that the study of reaper and its inhibitors provides valuable insights into the fundamental processes governing cell fate decisions, particularly in the context of developmental biology. While the specific chemical structures and characteristics of reaper inhibitors vary, their unified goal is to modulate the intricate cellular decision-making processes that determine survival or programmed death.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Z-VAD-FMK | 187389-52-2 | sc-3067 | 500 µg | $74.00 | 256 | |
Z-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. It can potentially prevent the activation of caspases downstream of reaper activation. | ||||||
Q-VD-OPH | 1135695-98-5 | sc-222230 | 5 mg | $782.00 | 5 | |
Q-VD-OPh is a potent, broad-spectrum caspase inhibitor. It can inhibit the caspase cascade that reaper might activate. | ||||||
Boc-Asp(OMe)-fluoromethyl ketone | 187389-53-3 | sc-214616 | 5 mg | $681.00 | ||
Boc-D-FMK is another caspase inhibitor that can prevent the activation of caspases in the apoptotic pathway where reaper plays a role. | ||||||
Necrostatin-1 | 4311-88-0 | sc-200142 sc-200142A | 20 mg 100 mg | $92.00 $336.00 | 97 | |
While Necrostatin-1 primarily inhibits necroptosis, it can also impact apoptotic pathways and might indirectly influence reaper-mediated apoptosis. | ||||||
Caspase-3 Inhibitor | 210344-95-9 | sc-3075 | 0.5 mg | $110.00 | 57 | |
Caspase-3 Inhibitor (Z-DEVD-FMK) is a caspase-3 inhibitor. Since caspase-3 is a critical executioner caspase, inhibiting it can counteract reaper's pro-apoptotic effects. | ||||||
Cyclosporin A | 59865-13-3 | sc-3503 sc-3503-CW sc-3503A sc-3503B sc-3503C sc-3503D | 100 mg 100 mg 500 mg 10 g 25 g 100 g | $62.00 $90.00 $299.00 $475.00 $1015.00 $2099.00 | 69 | |
Cyclosporin A inhibits the mitochondrial permeability transition pore, preventing cytochrome c release and caspase activation. This can indirectly influence reaper-mediated apoptosis. | ||||||
PD 150606 | 179528-45-1 | sc-222133 sc-222133A | 5 mg 25 mg | $116.00 $395.00 | 18 | |
PD 150606 is a selective, cell-permeable non-peptidic calpain inhibitor. It inhibits apoptosis by targeting calpains, potentially impacting the reaper-mediated apoptotic pathway. | ||||||