KRT222 inhibitors represent a class of chemical compounds designed to selectively target and interfere with the activity of KRT222. KRT222's precise biological functions and significance in cellular processes are subjects of ongoing research and exploration. These inhibitors are developed with the aim of modulating the function of KRT222, which could be involved in various molecular activities within cells, although specific details regarding its functions and interactions are still emerging.
The primary mechanism of action for KRT222 inhibitors typically involves their interaction with the KRT222 protein or its associated molecules, leading to the modulation of its normal function. By inhibiting KRT222, these compounds have the ability to influence cellular processes where this molecule plays a role, although researchers are still working to unravel the precise functions and molecular pathways associated with KRT222. Scientists studying KRT222 inhibitors aim to elucidate the specific roles and functions of KRT222 in cellular biology, contributing to our understanding of its significance within various physiological and pathological contexts. These inhibitors serve as valuable tools for advancing our knowledge of less-characterized proteins or molecules, enabling the exploration of new areas of molecular and cellular biology research. In this context, they contribute to expanding our understanding of the intricate world of cellular functions and molecular interactions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 intercalates into DNA, inhibiting RNA polymerase and thereby reducing mRNA synthesis, which could lower protein expression. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis by interfering with the translocation step in the ribosome, potentially decreasing protein levels. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine is incorporated into RNA and DNA and may cause demethylation and reactivation of silenced genes, but can also nonspecifically inhibit gene expression. | ||||||
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 (HDACs), altering chromatin structure and potentially downregulating certain genes. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid can modulate gene expression by activating nuclear receptors, leading to varied effects on cell differentiation and protein expression. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone is a glucocorticoid that can regulate gene transcription via glucocorticoid receptors, potentially affecting a range of genes. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $76.00 $255.00 | 18 | |
Hydroxyurea inhibits ribonucleotide reductase, decreasing the pool of deoxyribonucleotides and slowing down DNA synthesis and cell cycle progression. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol is a cyclin-dependent kinase inhibitor, which can lead to cell cycle arrest and potentially lower gene expression levels. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib inhibits the 26S proteasome, leading to increased cellular stress and potential downregulation of protein expression. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Vorinostat is an HDAC inhibitor, which can lead to changes in chromatin structure and potentially influence gene expression. | ||||||