HCG_1795065 Inhibitors represent a distinct chemical class designed to selectively target and inhibit the activity of a specific biomolecule identified by the designation hCG_1795065. This chemical class is characterized by compounds engineered to modulate the functions associated with hCG_1795065, contributing to a nuanced understanding of the biological processes in which this biomolecule is involved. The identification and development of inhibitors for hCG_1795065 are rooted in the broader field of molecular biology and pharmacology, aiming to elucidate the roles played by this particular biomolecule within cellular pathways.
To create effective inhibitors for hCG_1795065, researchers delve into the structural and functional characteristics of the biomolecule. This involves a detailed analysis of hCG_1795065's molecular structure and its interactions with other cellular components. The inhibitors are meticulously designed to interfere with these interactions, either by blocking binding sites or altering the conformation of hCG_1795065. By modulating the activity of hCG_1795065, these inhibitors serve as valuable tools in experimental settings, allowing scientists to investigate the specific functions and downstream effects associated with the targeted biomolecule. The research involving hCG_1795065 Inhibitors contributes to advancing our understanding of cellular processes, shedding light on the intricacies of molecular interactions and paving the way for potential applications in various scientific domains.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $131.00 $515.00 | 2 | |
RG108 is a DNA methyltransferase inhibitor, which can prevent the methylation of DNA, a process that is often associated with the silencing of genes, thereby potentially affecting protein expression. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $55.00 | 6 | |
Mithramycin A binds to DNA and inhibits RNA polymerase by preventing the binding of the enzyme to the DNA template, reducing the expression of genes. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $218.00 $322.00 $426.00 | 7 | |
Decitabine is a hypomethylating agent that can incorporate into DNA and inhibit DNA methyltransferase, leading to DNA demethylation and potentially affecting gene expression, including the downregulation of genes that are typically hypermethylated. | ||||||
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 | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
TSA is an inhibitor of histone deacetylase (HDAC), which can increase the acetylation of histones, leading to a more open chromatin structure and potentially affecting gene expression. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium butyrate is another HDAC inhibitor that can lead to increased histone acetylation and associated changes in gene expression. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $90.00 $212.00 | 24 | |
MS-275 is a selective HDAC inhibitor that can modify the acetylation state of histones, potentially altering gene expression profiles. | ||||||
Oxamflatin | 151720-43-3 | sc-205960 sc-205960A | 1 mg 5 mg | $151.00 $470.00 | 4 | |
Oxamflatin is an HDAC inhibitor that can induce hyperacetylation of histones and affect gene expression. | ||||||
C646 | 328968-36-1 | sc-364452 sc-364452A | 10 mg 50 mg | $265.00 $944.00 | 5 | |
C646 is a competitive inhibitor of histone acetyltransferase p300, which can lead to reduced histone acetylation and changes in gene expression. | ||||||
Scriptaid | 287383-59-9 | sc-202807 sc-202807A | 1 mg 5 mg | $64.00 $183.00 | 11 | |
Scriptaid is an HDAC inhibitor with a different chemical structure that can alter the acetylation state of histones, thereby influencing gene expression. | ||||||
Homocysteine | 6027-13-0 | sc-507315 | 250 mg | $195.00 | ||
SAH is a product inhibitor of S-adenosylmethionine-dependent methyltransferases, potentially affecting epigenetic regulation and gene expression. | ||||||