Abp ζ inhibitors are a distinct class of chemical compounds designed to target and inhibit the function of the Abp ζ protein, a member of the ATP-binding cassette (ABC) transporter family. These transporters play a key role in moving a variety of substrates, including ions, lipids, and small molecules, across cellular membranes, utilizing the energy derived from ATP hydrolysis. Abp ζ is believed to be responsible for the transport of specific molecules that are crucial for cellular functions, such as nutrient uptake, waste removal, and intracellular signaling. Inhibitors of Abp ζ work by blocking its ATPase activity or disrupting its conformational changes necessary for substrate transport, thereby preventing the movement of molecules across the cell membrane and altering the cellular processes dependent on these transport activities.
The chemical structure of Abp ζ inhibitors can vary, ranging from small organic molecules to more complex compounds specifically designed to bind with the ATP-binding or transmembrane domains of the protein. These inhibitors can function by competing with ATP for binding at the ATP-binding cassette, preventing the hydrolysis of ATP that provides the energy for transport. Alternatively, some inhibitors may bind to the transmembrane domain itself, blocking the passage of substrates through the transporter by interfering with the conformational changes necessary for its function. In some cases, inhibitors may also induce allosteric effects, altering the shape of Abp ζ in a way that disrupts its activity without directly blocking the active site. By inhibiting Abp ζ, these compounds allow researchers to better understand the structural and functional mechanisms underlying ABC transporter activity, as well as the broader role of these proteins in maintaining cellular balance and mediating the transport of critical molecules.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $62.00 $225.00 $779.00 | 24 | |
Nutlin-3 disrupts the interaction between p53 and MDM2, stabilizing p53 and restoring its tumor suppressor function in cells with wild-type p53. | ||||||
Pifithrin-μ | 64984-31-2 | sc-203195 sc-203195A | 10 mg 50 mg | $130.00 $379.00 | 4 | |
Pifithrin-μ inhibits p53 by blocking its transactivation domain, useful in contexts where p53 is pathologically activated. | ||||||
2-Amino-6-chloro-α-cyano-3-(ethoxycarbonyl)-4H-1-benzopyran-4-acetic Acid Ethyl Ester | 305834-79-1 | sc-479756 | 25 mg | $380.00 | ||
APR-246/PRIMA-1MET restores wild-type function to mutant p53, inducing apoptosis in tumor cells. | ||||||
Tenovin-6 | 1011557-82-6 | sc-224296 sc-224296A | 1 mg 5 mg | $272.00 $1214.00 | 9 | |
Tenovin-6 inhibits SIRT1 and SIRT2, leading to increased p53 acetylation and activation. | ||||||
COTI-2 | 1039455-84-9 | sc-507291 | 25 mg | $310.00 | ||
COTI-2 acts as a thiosemicarbazone that can reactivate mutant p53 to a wild-type conformation. | ||||||
Sirtinol | 410536-97-9 | sc-205976 sc-205976A | 1 mg 5 mg | $38.00 $113.00 | 14 | |
Sirtinol inhibits SIRT1, a deacetylase that deactivates p53, thus potentially increasing p53 activity. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $82.00 $216.00 $416.00 | 48 | |
SCH 51344 activates p53 by inducing a heat shock response, potentially leading to cancer cell death. | ||||||
SRPIN 340 | 218156-96-8 | sc-394310 | 10 mg | $226.00 | 1 | |
CP-31398 stabilizes the active conformation of p53, promoting its tumor suppressor functions. | ||||||
NSC-59984 | 803647-40-7 | sc-507310 | 10 mg | $230.00 | ||
NSC59984 disrupts p53-MDM2 interaction and reactivates p53 pathway in p53 wild-type tumors. | ||||||