KBTBD7 inhibitors are a class of chemical compounds that specifically target the protein kelch repeat and BTB (POZ) domain-containing 7 (KBTBD7). This protein belongs to the family of BTB-Kelch proteins, which are involved in a variety of cellular processes, including protein-protein interactions and regulation of protein degradation via the ubiquitin-proteasome system. KBTBD7, like other members of the BTB-Kelch family, has a role in the modulation of cellular signaling pathways by acting as an adapter in ubiquitination complexes. Inhibitors of KBTBD7 are designed to disrupt its function, often by binding to its BTB or kelch domains, thereby preventing the protein from facilitating the degradation of target substrates. By interfering with this process, these inhibitors can affect cellular homeostasis and signaling cascades that are dependent on KBTBD7-mediated ubiquitination.
The structural diversity of KBTBD7 inhibitors is important for their specificity and affinity towards the target protein. These compounds often exhibit varying levels of selectivity for different domains within KBTBD7, allowing researchers to investigate the distinct biological functions that each domain may regulate. Inhibitor design often relies on structural biology techniques such as X-ray crystallography and molecular modeling to identify key binding pockets and interaction sites. The inhibition of KBTBD7 can lead to alterations in various intracellular pathways, and the study of these inhibitors is of interest for understanding the broader biological roles of BTB-Kelch proteins in protein degradation and cellular signaling. Researchers utilize KBTBD7 inhibitors as molecular tools to explore the underlying mechanisms of ubiquitination and its regulatory effects on cellular function.
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| 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 | $56.00 $260.00 $980.00 | 163 | |
A proteasome inhibitor, impacting protein degradation and ubiquitin-proteasome pathways. | ||||||
Lactacystin | 133343-34-7 | sc-3575 sc-3575A | 200 µg 1 mg | $165.00 $575.00 | 60 | |
Another proteasome inhibitor, used to study ubiquitin-dependent protein degradation. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
A specific proteasome inhibitor, used clinically for certain types of cancer. | ||||||
MLN 4924 | 905579-51-3 | sc-484814 | 1 mg | $280.00 | 1 | |
Inhibits the NEDD8-activating enzyme, affecting protein ubiquitination and stability. | ||||||
Cytochalasin D | 22144-77-0 | sc-201442 sc-201442A | 1 mg 5 mg | $145.00 $442.00 | 64 | |
An inhibitor of actin polymerization, affecting cytoskeletal dynamics. | ||||||
Colchicine | 64-86-8 | sc-203005 sc-203005A sc-203005B sc-203005C sc-203005D sc-203005E | 1 g 5 g 50 g 100 g 500 g 1 kg | $98.00 $315.00 $2244.00 $4396.00 $17850.00 $34068.00 | 3 | |
Binds to tubulin and inhibits microtubule polymerization, impacting cell division and cytoskeletal structure. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $58.00 $83.00 $140.00 $242.00 | 38 | |
A microtubule-depolymerizing agent, used to disrupt microtubule dynamics. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
A ROCK inhibitor, affecting actin cytoskeleton organization and cell motility. | ||||||
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $40.00 $73.00 $217.00 $242.00 $724.00 $1196.00 | 39 | |
Stabilizes microtubules, preventing their disassembly which is essential for cell division. | ||||||
(S)-(−)-Blebbistatin | 856925-71-8 | sc-204253 sc-204253A sc-204253B sc-204253C | 1 mg 5 mg 10 mg 25 mg | $71.00 $260.00 $485.00 $949.00 | ||
Inhibits myosin II, affecting muscle contraction and cell motility. | ||||||