DUE-B inhibitors are a class of chemical compounds that specifically target the DNA unwinding element-binding protein (DUE-B), a crucial player in DNA replication initiation. DUE-B is involved in the regulation of the DNA unwinding process, binding to DNA unwinding elements (DUEs) at origins of replication. This protein plays an essential role in the formation of replication complexes and the unwinding of DNA strands, which is a key step in preparing the DNA for replication. Inhibitors of DUE-B function by interfering with its binding to DUEs or its interactions with other proteins in the replication complex, leading to disruption of the DNA replication process at the initiation stage.
The design and synthesis of DUE-B inhibitors require detailed knowledge of the protein's structure, particularly its DNA-binding domains and interaction surfaces. These inhibitors are developed to selectively bind to the active site or other functional regions of DUE-B, blocking its ability to participate in the formation of the replication complex. Structural biology techniques, such as X-ray crystallography or nuclear magnetic resonance (NMR), are often employed to determine the precise three-dimensional configuration of DUE-B, enabling the rational design of inhibitors with high specificity and potency. By inhibiting DUE-B, these compounds can modulate the regulation of DNA replication, providing valuable insights into the molecular mechanisms governing cell division and the maintenance of genomic integrity. The study of DUE-B inhibition offers researchers an important tool for exploring the intricacies of DNA replication and cellular proliferation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A inhibits histone deacetylases, leading to hyperacetylation of histones and potentially repressing DUE-B transcription. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine incorporates into DNA, inhibiting DNA methyltransferase and thus may reduce DUE-B gene methylation and expression. | ||||||
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D binds to DNA and halts RNA polymerase movement, which could suppress DUE-B mRNA synthesis. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin specifically inhibits RNA polymerase II, which could decrease DUE-B mRNA transcription. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Sirolimus binds to mTOR and may downregulate DUE-B expression by inhibiting mTOR signaling pathways. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine can alkalize lysosomes and may reduce DUE-B expression by interfering with lysosomal degradation of transcription factors. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide has been shown to inhibit transcription factors and may downregulate DUE-B expression by this mechanism. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG132 is a proteasome inhibitor which may lead to the accumulation of repressive transcriptional regulators, decreasing DUE-B expression. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Mithramycin A binds to GC-rich DNA sequences and may prevent transcription factors from binding to the DUE-B promoter. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD98059 is a MEK inhibitor that may alter transcription factor activity, potentially reducing DUE-B expression. | ||||||