Date published: 2026-4-1

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NUDT13 Inhibitors

NUDT13 inhibitors belong to a category of chemical compounds designed to interact with the NUDT13 enzyme, a member of the Nudix hydrolase family. The Nudix enzymes are characterized by their ability to hydrolyze various nucleoside diphosphate derivatives, which are implicated in a wide array of intracellular processes. Specifically, NUDT13 is an enzyme that has been identified as having a role in the metabolism of RNA and DNA building blocks, or nucleotides. Inhibitors targeting NUDT13 are meticulously engineered to bind to the active site of this enzyme, thereby blocking its normal function. They are shaped in such a way that they mimic the natural substrates of the enzyme but are not processed in the same way, thus effectively 'jamming' the enzymatic machinery. This inhibition can affect the regulation of the enzyme's substrates and, consequently, alter the balance of nucleotide pools within the cell. The precise mechanism of inhibition often involves the formation of stable complexes between the inhibitor and the NUDT13 enzyme, which prevents the proper enzymatic activity from occurring. The development and study of NUDT13 inhibitors are rooted in the intricate field of biochemistry and molecular biology, which seeks to understand the fundamental processes of life at a molecular level. These inhibitors are typically the result of rational drug design, where computational models of the NUDT13 enzyme's structure guide the synthesis of molecules that could interact with its active site. Extensive research goes into characterizing the binding affinity, specificity, and stability of these inhibitors in relation to the enzyme. Studies often involve a combination of x-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and computational docking simulations to elucidate the precise interactions between the enzyme and the inhibitor. Such detailed investigations help to refine the molecular structure of the inhibitors for increased efficacy in their specific role of enzyme inhibition.

Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Sulindac

38194-50-2sc-202823
sc-202823A
sc-202823B
1 g
5 g
10 g
$32.00
$86.00
$150.00
3
(1)

Sulindac sulfide inhibits the Wnt signaling pathway by targeting the Dishevelled protein. Since NUDT13 is potentially associated with the regulation of gene expression, its activity could be diminished as a downstream effect of Wnt pathway inhibition.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

EGCG, a major component of green tea, has been shown to interfere with the NF-κB pathway, which is involved in the expression of various genes, including potentially those regulated by NUDT13. By inhibiting NF-κB, EGCG may indirectly decrease NUDT13's functional activity.

XAV939

284028-89-3sc-296704
sc-296704A
sc-296704B
1 mg
5 mg
50 mg
$36.00
$117.00
$525.00
26
(1)

XAV-939 is a tankyrase inhibitor that stabilizes Axin by preventing its poly(ADP-ribosyl)ation, leading to the downregulation of Wnt signaling. Given that NUDT13 may play a role in gene regulation downstream of Wnt, XAV-939 might lead to reduced NUDT13 activity.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

PD98059 is a MEK inhibitor that blocks the MAPK/ERK pathway, a key signaling route for cell proliferation and differentiation. NUDT13, if implicated in these processes, could be affected by the reduced activation of this pathway.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

LY294002 is a PI3K inhibitor that could lead to decreased AKT phosphorylation, thereby affecting the cell survival pathways that might involve NUDT13. As a result, NUDT13's role in these pathways could be indirectly inhibited.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Rapamycin is an mTOR inhibitor that can disrupt the mTOR signaling pathway, which is crucial for cell growth and proliferation. If NUDT13 is involved in such pathways, its activity would be reduced as a consequence of mTOR inhibition.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

Y-27632 is a ROCK inhibitor, and by inhibiting Rho-associated kinases, it can modulate cytoskeletal dynamics. NUDT13, should it be linked to these processes, might have reduced activity due to alterations in cytoskeletal regulation.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$135.00
$1085.00
115
(2)

Bortezomib is a proteasome inhibitor that can lead to the accumulation of misfolded proteins, potentially affecting protein turnover and functions related to NUDT13.

Cyclopamine

4449-51-8sc-200929
sc-200929A
1 mg
5 mg
$94.00
$208.00
19
(1)

Cyclopamine inhibits the Hedgehog signaling pathway by binding to Smoothened. If NUDT13 is implicated in gene expression mediated by Hedgehog signaling, its activity could be dampened by cyclopamine.

BML-275

866405-64-3sc-200689
sc-200689A
5 mg
25 mg
$96.00
$355.00
69
(1)

Dorsomorphin is an inhibitor of BMP signaling by targeting the ALK2, ALK3, and ALK6 receptors. By interfering with this pathway, it could indirectly affect the functional activity of NUDT13 if it is involved in BMP-mediated processes.