MOMP inhibitors are a specialized class of compounds designed to target the mitochondrial outer membrane permeabilization (MOMP) process, a critical event in the regulation of cellular apoptosis. The identification and development of these inhibitors involve a sophisticated interplay of biochemical, computational, and cellular techniques, aimed at understanding and modulating the intricate mechanisms underlying MOMP. The journey begins with the application of high-throughput screening methods, where vast libraries of chemical compounds are assessed for their ability to interfere with or inhibit the MOMP process. This screening is crucial for isolating potential inhibitors that show promise in modulating this critical cellular pathway. Following the identification of these promising compounds, they are subjected to rigorous molecular docking and dynamics simulations. These computational models provide a window into the molecular interactions between the inhibitors and their target components within the mitochondrial membrane, offering insights into binding affinities, interaction sites, and the potential for inducing conformational changes that could inhibit MOMP.
In addition to in vitro studies, the potential MOMP inhibitors are further evaluated in cellular models to ascertain their effects on apoptosis and mitochondrial function. Techniques such as CRISPR-Cas9 gene editing enable the creation of cell lines with altered expressions of key proteins involved in MOMP, providing a detailed landscape to study how these inhibitors impact the process in a controlled environment. Fluorescent tagging of proteins associated with MOMP allows for real-time visualization of the inhibitors' effects on the mitochondrial membrane and the apoptotic process. These cellular studies are invaluable for confirming the efficacy of the MOMP inhibitors observed in biochemical assays and computational predictions, offering a holistic view of how these compounds interact with the mitochondrial apoptosis machinery. Through this comprehensive methodology, MOMP inhibitors are meticulously characterized, shedding light on their mechanism of action and advancing our understanding of their role in modulating apoptosis.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 | $118.00 $337.00 $520.00 $832.00 $1632.00 | 10 | |
ABT-199 is a BH3 mimetic and a Bcl-2-selective inhibitor with a subnanomolar affinity Ki of <0.01 nM. | ||||||
ABT 263 | 923564-51-6 | sc-207241 | 5 mg | $245.00 | 16 | |
ABT 263 is an inhibitor of antiapoptotic Bcl-2 proteins | ||||||
WEHI-539 | 1431866-33-9 | sc-507317 | 5 mg | $233.00 | ||
Specifically binds to and inhibits Bcl-xL, promoting apoptosis by freeing pro-apoptotic proteins to trigger MOMP. | ||||||
Obatoclax Mesylate | 803712-79-0 | sc-364221 sc-364221A | 5 mg 10 mg | $96.00 $141.00 | ||
A pan-Bcl-2 inhibitor, it targets Bcl-2, Bcl-xL, and Bcl-w, disrupting their anti-apoptotic function and facilitating MOMP. | ||||||
TW-37 | 877877-35-5 | sc-361387 sc-361387A | 10 mg 50 mg | $200.00 $860.00 | 2 | |
A small molecule inhibitor targeting Bcl-2, Bcl-xL, and Mcl-1, disrupting their anti-apoptotic activity and promoting apoptosis. | ||||||
S63845 | 1799633-27-4 | sc-507518 | 1 mg | $150.00 | ||
Selectively targets Mcl-1, a key regulator in MOMP, promoting apoptosis by inhibiting Mcl-1's interaction with pro-apoptotic proteins. | ||||||
UMI-77 | 518303-20-3 | sc-507475 | 5 mg | $130.00 | ||
This molecule targets Mcl-1, disrupting its interaction with pro-apoptotic proteins and thus promoting apoptosis. | ||||||
A-1331852 | 1430844-80-6 | sc-507472 | 5 mg | $230.00 | ||
Selectively inhibits Bcl-xL, disrupting its anti-apoptotic function and promoting MOMP. | ||||||
A-1210477 | 1668553-26-1 | sc-507474 | 5 mg | $195.00 | ||
A potent and selective Mcl-1 inhibitor, it disrupts Mcl-1’s interaction with pro-apoptotic proteins, facilitating apoptosis. | ||||||