Date published: 2026-1-23

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DPRP1 Inhibitors

DPRP1 inhibitors represent a class of compounds that specifically target the DNA Polymerase Rev1 Protein 1 (DPRP1), a key enzyme involved in translesion synthesis (TLS), a process that allows DNA replication to continue past a site of damage or lesion. DPRP1 plays a critical role in the error-prone DNA repair pathways, particularly during instances where the replication machinery encounters DNA damage that stalls replication forks. The enzyme facilitates the insertion of nucleotides opposite damaged bases, helping the cell to bypass the lesion but often at the cost of introducing mutations. By inhibiting DPRP1, these compounds interfere with the enzyme's function, thereby potentially reducing the cell's ability to bypass lesions during DNA replication. This action can be particularly significant in the context of understanding cellular responses to DNA damage, as well as exploring the fundamental processes of mutagenesis, DNA repair, and the maintenance of genomic stability. Inhibitors of DPRP1 are typically characterized by their ability to bind to the enzyme's active site or allosteric sites, effectively blocking its interaction with DNA or other associated proteins involved in the TLS pathway. Structural studies often reveal that these inhibitors can vary widely in their chemical makeup, ranging from small molecules to more complex structures, each tailored to exploit specific interactions within the enzyme's binding sites. The inhibition of DPRP1 provides researchers with valuable tools to dissect the mechanisms by which cells manage DNA damage and the fidelity of DNA replication. Moreover, these inhibitors serve as important probes for studying the intricate balance between DNA repair pathways and replication processes, helping to elucidate the roles of different proteins and enzymes in maintaining the integrity of the genome under conditions of stress and damage.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Vildagliptin

274901-16-5sc-208485
10 mg
$176.00
4
(1)

Vildagliptin, a selective DPP-4 inhibitor, exhibits unique molecular interactions that enhance its binding affinity to the enzyme's active site. Its structure allows for specific hydrogen bonding and hydrophobic interactions, facilitating a stable enzyme-inhibitor complex. The kinetics of Vildagliptin demonstrate a rapid onset of action, with a notable half-life that supports sustained inhibition. This compound's distinct conformational flexibility contributes to its efficacy in modulating enzymatic pathways.

Nifedipine

21829-25-4sc-3589
sc-3589A
1 g
5 g
$59.00
$173.00
15
(1)

Calcium channel blocker that might affect intracellular signaling and post-translational modifications.

PD 98059

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

MEK inhibitor affecting the MAPK/ERK pathway, potentially influencing proteins in related pathways.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

PI3K inhibitor, affecting multiple cellular processes that might be associated with protein modifications.

LY 294002

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

Another PI3K inhibitor affecting cellular processes that may impact post-translational modifications.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

JNK inhibitor potentially influencing pathways related to protein modifications.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

p38 MAPK inhibitor which may impact pathways related to protein modifications.

Rapamycin

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

mTOR inhibitor affecting protein synthesis and potentially related post-translational modifications.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$64.00
$246.00
136
(2)

MEK1/2 inhibitor potentially influencing proteins in related modification pathways.

Calyculin A

101932-71-2sc-24000
sc-24000A
10 µg
100 µg
$163.00
$800.00
59
(3)

Protein phosphatase inhibitor that could influence multiple protein modification pathways.