Date published: 2025-10-11

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Cdt2 Inhibitors

Cdt2 inhibitors represent a group of compounds that indirectly interfere with the function of the Cdt2 protein. These inhibitors act through various mechanisms to disrupt the cellular processes in which Cdt2 is involved. For instance, they target the neddylation process that is crucial for the activation of Cullin-RING ligases, including the CRL4^Cdt2 complex. By inhibiting the NEDD8-activating enzyme, inhibitors effectively block the neddylation that is necessary for Cdt2 to function properly. Inhibitors influence a myriad of signaling pathways that indirectly affect Cdt2 function.

Cdt2 inhibitors may alter the synthesis and degradation balance of proteins, including those involved in the pathways Cdt2 regulates. Inhibitors exert their influence by modulating the cell cycle and gene expression, respectively. Inhibitors impact the cell's response to oxidative stress, which could influence the expression and function of proteins that interact with Cdt2 or are part of its regulatory network. In summary, Cdt2 inhibitors encompass a diverse array of chemical agents that share the common feature of indirectly impeding the function of the Cdt2 protein. These inhibitors work through a variety of mechanisms, including but not limited to, hindering the neddylation process, proteasome function, cell cycle regulation, gene expression modulation, and stress response pathways. These inhibitors have a distinct mode of action, yet they collectively contribute to the suppression of Cdt2 activity by affecting the protein's ability to regulate its substrates within the cell.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

MLN 4924

905579-51-3sc-484814
1 mg
$280.00
1
(0)

MLN4924 inhibits NEDD8-activating enzyme, preventing neddylation of Cullin proteins, which is essential for CRL4^Cdt2 complex function.

Bortezomib

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

Bortezomib inhibits the proteasome, leading to an accumulation of Cdt2 substrates, indirectly affecting the functional cycling of Cdt2.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$56.00
$260.00
$980.00
163
(3)

MG132 is a proteasome inhibitor that causes an increase in the levels of ubiquitinated proteins, indirectly hindering Cdt2's ability to target new substrates.

Lactacystin

133343-34-7sc-3575
sc-3575A
200 µg
1 mg
$165.00
$575.00
60
(2)

Lactacystin is another proteasome inhibitor that can lead to the buildup of Cdt2 substrates, impairing Cdt2-mediated ubiquitination indirectly.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$36.00
$68.00
$107.00
$214.00
$234.00
$862.00
$1968.00
47
(1)

Curcumin can modulate multiple signaling pathways and may affect Cdt2 indirectly by altering protein synthesis and degradation pathways.

Roscovitine

186692-46-6sc-24002
sc-24002A
1 mg
5 mg
$92.00
$260.00
42
(2)

Roscovitine inhibits cyclin-dependent kinases, which can affect cell cycle progression and, in turn, the turnover of Cdt2 substrates.

Thalidomide

50-35-1sc-201445
sc-201445A
100 mg
500 mg
$109.00
$350.00
8
(0)

Thalidomide and its analogs bind to the E3 ubiquitin ligase Cereblon, potentially affecting the ubiquitination process related to Cdt2.

Nutlin-3

548472-68-0sc-45061
sc-45061A
sc-45061B
1 mg
5 mg
25 mg
$56.00
$212.00
$764.00
24
(1)

Nutlin-3 disrupts the MDM2-p53 interaction, which can stabilize p53 and influence Cdt2's regulation of cell cycle-related proteins.

Palbociclib

571190-30-2sc-507366
50 mg
$315.00
(0)

Palbociclib is a CDK4/6 inhibitor that can alter cell cycle progression, potentially impacting Cdt2 substrate availability and function.

Suberoylanilide Hydroxamic Acid

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

Suberoylanilide Hydroxamic Acid is a histone deacetylase inhibitor that can change the expression levels of various proteins, including those involved in Cdt2-mediated pathways.