Date published: 2025-12-19

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MTBP Inhibitors

MTBP inhibitors belong to a specific chemical class of compounds designed to selectively target and modulate the activity of MTBP (Mdm2-binding protein), a critical protein involved in cellular processes such as DNA replication and cell cycle progression. MTBP plays a crucial role in the interaction between p53 and Mdm2, two key regulatory proteins that are central to cell growth control and DNA damage response. By inhibiting MTBP, these compounds aim to disrupt its interaction with Mdm2 and potentially influence cellular pathways associated with DNA stability and cell division.

The development of MTBP inhibitors involves a multifaceted approach, encompassing aspects of structural biology, computational modeling, and high-throughput screening. Researchers utilize techniques such as X-ray crystallography or nuclear magnetic resonance (NMR) to gain insights into the three-dimensional structure of the MTBP-Mdm2 complex. This structural information guides the rational design of inhibitors that can bind to specific regions of MTBP and interfere with its interaction with Mdm2. Computational methods, including molecular docking and virtual screening, contribute to the identification of potential inhibitor candidates. These compounds are designed to selectively bind to MTBP and stop its association with Mdm2, potentially altering downstream signaling pathways. These investigations contribute to a deeper understanding of the role of MTBP in cell cycle control and DNA integrity.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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 is a small molecule that disrupts the interaction between Mdm2 and p53, thereby preventing p53 degradation. While it's primarily an Mdm2 inhibitor, it indirectly affects MTBP activity by promoting p53 stabilization.

Tenovin-6

1011557-82-6sc-224296
sc-224296A
1 mg
5 mg
$272.00
$1214.00
9
(1)

Tenovins are compounds that increase p53 levels by targeting SIRT1, a protein deacetylase. Tenovin-6, a member of the tenovin family, has demonstrated inhibition of MTBP and activation of p53-mediated apoptosis.