DPPA2 inhibitors encompass a class of chemical compounds that specifically target and impede the function of the Developmental Pluripotency Associated 2 (DPPA2) protein. The DPPA2 protein is known to be involved in the regulation of gene expression, particularly in the maintenance of pluripotency in stem cells. It is a factor that can bind to DNA and influence the transcriptional machinery of the cell, potentially affecting the expression of genes that contribute to the stem cell's unique properties. The inhibition of DPPA2 is brought about by molecules that can interfere with its ability to bind to DNA or its interaction with other proteins that are part of the transcriptional complex. Inhibitors may act by directly binding to the DPPA2 protein, thereby preventing its association with chromatin, or by altering its conformation so that its functional domains are unable to engage in their normal interactions.
The development of DPPA2 inhibitors requires detailed insights into the protein's structural domains that are responsible for DNA binding and protein-protein interactions. By utilizing techniques such as X-ray crystallography or cryo-electron microscopy, researchers can obtain high-resolution images of the DPPA2 protein and identify critical regions amenable to inhibitor binding. Molecules designed to inhibit DPPA2 typically mimic the natural substrates or binding partners of the protein, but with modifications that prevent functional engagement. These modifications can include the addition of bulky side groups that create steric hindrance, or chemical groups that induce charge-charge repulsions, preventing the proper alignment of DPPA2 with its target sequences or interaction partners. Chemical properties such as bioavailability, stability, and cell permeability are also key considerations in the development of DPPA2 inhibitors, as these factors influence the compound's ability to reach its intracellular target and exert the desired inhibitory effect.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
GSK-3 Inhibitor XVI | 252917-06-9 | sc-221691 sc-221691A | 5 mg 25 mg | $153.00 $520.00 | 4 | |
A GSK3β inhibitor. By inhibiting GSK3β, it stabilizes β-catenin and influences the Wnt signaling pathway. Pluripotency factors including DPPA2 can be modulated through this action. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Rho-associated protein kinase (ROCK) inhibitor. ROCK plays a role in cell adhesion and morphology which can indirectly influence pluripotency markers like DPPA2. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $80.00 $212.00 $408.00 | 48 | |
An inhibitor of the TGF-β receptor. It blocks the TGF-β signaling pathway which is involved in cell differentiation, potentially affecting DPPA2 expression. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
PI3K inhibitor. The PI3K/AKT pathway has roles in cell survival and pluripotency, so inhibiting this pathway can indirectly modulate proteins associated with pluripotency. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
A JNK inhibitor. The JNK pathway influences cell differentiation and apoptosis. By modulating this pathway, pluripotency-associated proteins may be indirectly influenced. | ||||||
BIX01294 hydrochloride | 1392399-03-9 | sc-293525 sc-293525A sc-293525B | 1 mg 5 mg 25 mg | $36.00 $110.00 $400.00 | ||
A G9a histone methyltransferase inhibitor. Epigenetic changes, such as histone modifications, can impact pluripotency-associated genes including DPPA2. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
A DNA methyltransferase inhibitor. By altering DNA methylation, it can affect the expression of pluripotency-related genes. | ||||||
SC1 (Pluripotin) | 839707-37-8 | sc-255607 sc-255607A sc-255607B sc-255607C | 1 mg 5 mg 10 mg 25 mg | $164.00 $195.00 $464.00 $764.00 | ||
A dual ERK1 and GSK3β inhibitor. Influencing these pathways can indirectly modulate pluripotency factors and associated proteins. | ||||||
Gö 6983 | 133053-19-7 | sc-203432 sc-203432A sc-203432B | 1 mg 5 mg 10 mg | $103.00 $293.00 $465.00 | 15 | |
A broad-spectrum PKC inhibitor. PKC signaling influences various cellular processes, including those associated with pluripotency. | ||||||
3-Deazaneplanocin, HCl salt | 120964-45-6 | sc-351856 sc-351856A sc-351856B | 1 mg 5 mg 10 mg | $251.00 $600.00 $918.00 | 2 | |
An inhibitor of the S-adenosylhomocysteine hydrolase. This affects methylation processes and can thus modulate genes associated with pluripotency. | ||||||