CENPBD1 inhibitors are a class of chemical compounds designed to specifically target and inhibit the function of the CENPBD1 protein, a component closely associated with the centromere and involved in the regulation of chromosome segregation during cell division. CENPBD1, or Centromere Protein Binding Domain 1, plays a key role in the assembly and maintenance of the kinetochore, a crucial structure that connects chromosomes to spindle microtubules, ensuring accurate distribution of chromosomes during mitosis. Inhibition of CENPBD1 disrupts its interaction with other centromeric proteins, which can influence the structural integrity of the kinetochore and alter the dynamics of chromosome movement during cell division.
Mechanistically, CENPBD1 inhibitors function by binding to specific domains of the protein, particularly those involved in its interaction with centromeric DNA or associated proteins, such as other components of the kinetochore complex. This binding can interfere with the normal assembly of the kinetochore or hinder its ability to recruit necessary molecules for chromosome segregation. By inhibiting CENPBD1, these compounds help to dissect the specific contributions of this protein to centromere function and kinetochore architecture. Researchers use CENPBD1 inhibitors to explore the detailed molecular pathways that govern chromosomal stability, especially during mitosis, when the accuracy of chromosome segregation is critical for maintaining genomic integrity. These inhibitors provide valuable insights into the role of CENPBD1 in the broader framework of cellular division and the mechanisms that ensure proper chromosome alignment and separation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
Inhibits CDK4/6, which are involved in cell cycle regulation. CENPBD1, associated with centromere protein function, may be indirectly affected by cell cycle alterations. | ||||||
Roscovitine | 186692-46-6 | sc-24002 sc-24002A | 1 mg 5 mg | $92.00 $260.00 | 42 | |
Targets CDKs and could disrupt cell cycle progression, thereby influencing CENPBD1 activity in chromosome segregation. | ||||||
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 and can disrupt chromosome dynamics. As CENPBD1 is linked to chromosome function, this stabilization can hinder its role. | ||||||
Monastrol | 254753-54-3 | sc-202710 sc-202710A | 1 mg 5 mg | $120.00 $233.00 | 10 | |
Inhibits kinesin Eg5, affecting spindle formation and potentially impacting CENPBD1's role in mitosis. | ||||||
BI 2536 | 755038-02-9 | sc-364431 sc-364431A | 5 mg 50 mg | $148.00 $515.00 | 8 | |
Inhibits PLK1, a key regulator of mitotic progression, thereby potentially affecting CENPBD1's function in cell division. | ||||||
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 | |
Disrupts microtubule polymerization, which can alter mitotic spindle organization and affect CENPBD1's function in chromosome segregation. | ||||||
S-Trityl-L-cysteine | 2799-07-7 | sc-202799 sc-202799A | 1 g 5 g | $31.00 $65.00 | 6 | |
A kinesin spindle protein inhibitor, which can disrupt mitotic spindle dynamics, potentially impacting CENPBD1's role in cell division. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
Aurora kinase inhibitor that affects chromosome alignment and segregation, processes in which CENPBD1 is potentially involved. | ||||||
Tozasertib | 639089-54-6 | sc-358750 sc-358750A | 25 mg 50 mg | $61.00 $85.00 | 4 | |
Targets Aurora kinases, which are involved in cell cycle progression, potentially affecting CENPBD1's associated activities. | ||||||
MLN8237 | 1028486-01-2 | sc-394162 | 5 mg | $220.00 | ||
Inhibits Aurora A kinase, impacting mitotic spindle assembly and chromosome segregation, thereby possibly affecting CENPBD1 function. | ||||||