Bclp2 inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the Bclp2 protein, which is part of the Bcl-2 family of proteins. Bclp2 is involved in regulating key cellular processes, particularly those associated with apoptosis and cell survival. As with other members of the Bcl-2 family, Bclp2 functions by controlling the balance between pro-apoptotic and anti-apoptotic signals within cells. It is located primarily at the outer membrane of mitochondria, where it influences mitochondrial integrity and the release of apoptogenic factors. By inhibiting Bclp2, these compounds prevent the protein from performing its regulatory role, thereby altering the cell's response to internal stress and apoptotic signals. This makes Bclp2 inhibitors useful for studying the mechanisms behind cell death regulation and mitochondrial dynamics.
Bclp2 inhibitors are designed to bind to specific regions of the Bclp2 protein, such as its BH3 domain, which is essential for its interaction with other apoptotic regulators. These inhibitors are developed through structure-activity relationship (SAR) studies to improve their binding affinity and selectivity for Bclp2, minimizing the impact on other proteins within the Bcl-2 family. The inhibition of Bclp2 allows researchers to explore its role in maintaining mitochondrial stability, its interactions with other proteins involved in apoptosis, and how the cell's decision to undergo programmed cell death is regulated. Bclp2 inhibitors are instrumental in investigating the broader cellular processes related to apoptosis and mitochondrial function, providing deeper insights into how cells regulate their survival in response to various internal and external stimuli.
SEE ALSO...
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Obatoclax Mesylate | 803712-79-0 | sc-364221 sc-364221A | 5 mg 10 mg | $94.00 $138.00 | ||
A small molecule inhibitor that influences the Bcl-2 protein by binding to its BH3 domain, disrupting its anti-apoptotic function and promoting apoptosis. | ||||||
ABT-199 | 1257044-40-8 | sc-472284 sc-472284A sc-472284B sc-472284C sc-472284D | 1 mg 5 mg 10 mg 100 mg 3 g | $116.00 $330.00 $510.00 $816.00 $1632.00 | 10 | |
A selective Bcl-2 inhibitor that targets the BH3 binding groove, preventing its interaction with pro-apoptotic proteins and promoting programmed cell death. | ||||||
S63845 | 1799633-27-4 | sc-507518 | 1 mg | $150.00 | ||
A potent and specific Bcl-2 inhibitor that hinders its anti-apoptotic activity, inducing apoptosis in cancer cells with elevated Bcl-2 expression. | ||||||
TW-37 | 877877-35-5 | sc-361387 sc-361387A | 10 mg 50 mg | $200.00 $860.00 | 2 | |
A small molecule inhibitor that disrupts the Bcl-2/BH3 interaction, leading to the activation of pro-apoptotic signals and triggering apoptosis. | ||||||
HA14-1 | 65673-63-4 | sc-205911 sc-205911A | 5 mg 25 mg | $58.00 $205.00 | ||
An organic compound that inhibits Bcl-2 by binding to its hydrophobic cleft, disrupting the anti-apoptotic function and promoting cell death. | ||||||
AT-101 | 90141-22-3 | sc-507316 | 10 mg | $160.00 | ||
A small molecule inhibitor that targets Bcl-2, disrupting its anti-apoptotic function and sensitizing cancer cells to undergo programmed cell death. | ||||||
WEHI-539 | 1431866-33-9 | sc-507317 | 5 mg | $233.00 | ||
A BH3 mimetic compound that selectively inhibits Bcl-2, disrupting its anti-apoptotic function and promoting cell death in cancer cells. | ||||||
UMI-77 | 518303-20-3 | sc-507475 | 5 mg | $130.00 | ||
A small molecule inhibitor that selectively targets Bcl-2, interfering with its anti-apoptotic activity and triggering apoptosis in cancer cells. | ||||||
ABT 737 | 852808-04-9 | sc-207242 | 2.5 mg | $200.00 | 54 | |
A small molecule inhibitor that mimics the BH3 domain, selectively binding to Bcl-2, Bcl-xL, and Bcl-w, inducing apoptosis in cancer cells. |