Date published: 2025-11-1

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HJURP Inhibitors

HJURP inhibitors are chemical compounds that interfere with the function of Holliday Junction Recognition Protein (HJURP), a critical protein involved in the deposition and stabilization of CENP-A, a histone H3 variant essential for centromere function and chromosome segregation during mitosis. HJURP acts as a chaperone, specifically guiding the incorporation of CENP-A into nucleosomes at the centromere, which is necessary for the proper formation of the kinetochore, a structure essential for chromosome attachment to the mitotic spindle. By inhibiting HJURP, these compounds can disrupt the accurate distribution of chromosomes during cell division, potentially leading to mitotic errors such as chromosome mis-segregation and aneuploidy. The molecular mechanisms of HJURP inhibition often involve blocking its interaction with CENP-A or other associated proteins, thereby preventing the correct localization and function of this crucial histone variant.

The development of HJURP inhibitors has provided valuable insights into the biological processes that underlie chromosomal stability. By studying the effects of these inhibitors, researchers can explore the precise role of HJURP in the cell cycle, particularly its contribution to centromere assembly and kinetochore function. Additionally, these inhibitors offer a window into understanding the broader implications of histone modification and nucleosome assembly in maintaining genomic integrity. HJURP's interaction with CENP-A, as well as its coordination with other centromeric proteins, is a key area of investigation. By manipulating this pathway with specific inhibitors, scientists can examine the effects on chromosome dynamics, mitotic progression, and overall cellular architecture, providing a foundation for further research into chromosomal behavior and the regulation of centromeric activity.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$65.00
$319.00
$575.00
$998.00
28
(1)

Through the activation of retinoic acid receptors, retinoic acid could initiate a cascade that leads to the downregulation of HJURP expression by changing gene transcription patterns.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

Rapamycin may inhibit mTOR signaling, which could lead to a reduction in protein synthesis and potentially a decrease in HJURP protein levels due to altered cellular growth signals.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

LY 294002, a PI3K inhibitor, could decrease AKT phosphorylation and subsequently downregulate transcription factors responsible for HJURP expression.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Bortezomib could lead to the accumulation of ubiquitinated proteins, possibly reducing the stability of factors that enhance HJURP expression, resulting in its decreased levels.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$130.00
$270.00
37
(2)

Suberoylanilide Hydroxamic Acid (Vorinostat) could lead to hyperacetylation of histones associated with the HJURP gene, which may result in the downregulation of its expression.

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
$38.00
$58.00
$102.00
$202.00
8
(1)

By binding to Hsp90, geldanamycin may destabilize its client proteins, which could include transcription factors required for the upregulation of HJURP, thus decreasing its expression.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$214.00
$316.00
$418.00
7
(1)

5-Aza-2′-Deoxycytidine (Decitabine) may decrease the methylation levels of the HJURP gene promoter, leading to reduced transcriptional activity and lower HJURP protein levels.

Cyclopamine

4449-51-8sc-200929
sc-200929A
1 mg
5 mg
$92.00
$204.00
19
(1)

Cyclopamine may inhibit the Hedgehog signaling pathway, resulting in the downregulation of target genes, including potentially the HJURP gene, leading to decreased expression.