EG434179 inhibitors are a class of chemical compounds designed to specifically inhibit the activity of the molecule EG434179, which likely plays a significant role in cellular regulation, particularly in processes involving protein interactions, enzymatic functions, or signaling pathways. Although the specific biological function of EG434179 may vary depending on the cellular context, it is assumed to be a key mediator in molecular processes that control cell growth, signal transduction, or metabolic pathways. The inhibition of EG434179 by these compounds disrupts its ability to interact with its substrates or binding partners, leading to changes in the pathways that it regulates. This class of inhibitors provides a useful tool for probing the role of EG434179 in maintaining cellular balance and investigating how its modulation can influence various cellular functions.
Structurally, EG434179 inhibitors are typically designed to interact with the molecule's active site or regulatory domains critical for its biological activity. These inhibitors may function through competitive inhibition, where they directly block the active site of EG434179, preventing it from engaging with its natural substrate. Alternatively, they may operate through non-competitive mechanisms, inducing conformational changes that reduce the molecule's efficiency in catalyzing reactions or mediating protein interactions. The use of EG434179 inhibitors enables researchers to observe the effects of blocking this molecule in different cellular contexts, revealing the downstream consequences of its inhibition on related biochemical networks. By studying these inhibitors, scientists can gain insights into the molecular pathways regulated by EG434179 and understand its role in maintaining cellular signaling, protein stability, and other essential functions necessary for proper cellular operation.
SEE ALSO...
| 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 | $74.00 $243.00 $731.00 $2572.00 $21848.00 | 53 | |
Inhibits RNA polymerase II activity by intercalating with DNA, preventing transcription initiation, ultimately disrupting Zfp975's role as a DNA-binding transcription factor. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $269.00 $1050.00 | 26 | |
A potent inhibitor of RNA polymerase II, blocking transcription by preventing RNA chain elongation, thereby impeding Zfp975's ability to bind to cis-regulatory regions and regulate gene expression. | ||||||
Flavopiridol Hydrochloride | 131740-09-5 | sc-207687 | 10 mg | $317.00 | ||
Indirect inhibitor influencing cellular signaling pathways associated with transcriptional regulation. Modulates cyclin-dependent kinases, disrupting the precise regulatory network involved in Zfp975's function. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Modulates various cellular pathways related to transcriptional regulation, indirectly affecting Zfp975 by influencing signaling cascades, leading to alterations in its DNA-binding transcription factor activity. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Inhibits RNA polymerase II transcription, directly impacting Zfp975's function by disrupting the fundamental machinery involved in gene expression and cis-regulatory region binding. | ||||||
Fludarabine | 21679-14-1 | sc-204755 sc-204755A | 5 mg 25 mg | $58.00 $204.00 | 15 | |
Affects nucleotide metabolism, influencing cellular processes that indirectly impact Zfp975's role in transcriptional regulation by RNA polymerase II. | ||||||
DRB | 53-85-0 | sc-200581 sc-200581A sc-200581B sc-200581C | 10 mg 50 mg 100 mg 250 mg | $43.00 $189.00 $316.00 $663.00 | 6 | |
Inhibits RNA polymerase II elongation, disrupting the transcriptional machinery and impairing Zfp975's ability to bind to cis-regulatory regions and regulate gene expression. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $231.00 $863.00 | 1 | |
A bromodomain inhibitor influencing chromatin structure and transcriptional regulation. Disrupts Zfp975's function by interfering with the epigenetic landscape and cis-regulatory region accessibility. | ||||||
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 | |
Inhibits histone deacetylases, impacting chromatin structure and accessibility of cis-regulatory regions. Indirectly affects Zfp975 by modifying the epigenetic landscape and influencing its DNA-binding transcription factor activity. | ||||||