Rslcan-6 inhibitors represent a class of small molecules or compounds specifically designed to interfere with the function of Rslcan-6, a protein involved in various intracellular signaling pathways. Rslcan-6, like many proteins, plays a pivotal role in regulating cell signaling, particularly in processes related to cell proliferation, differentiation, and migration. The inhibitors of this protein are engineered to bind to its active or allosteric sites, disrupting its ability to participate in signaling cascades that are crucial for cellular communication. By modulating the activity of Rslcan-6, these inhibitors can induce significant changes in the behavior of cells, particularly those that are highly dependent on Rslcan-6-mediated pathways. This inhibition can be highly specific, depending on the structure of both the protein and the inhibitor, which enables precise targeting of particular cellular functions.
The molecular design of Rslcan-6 inhibitors typically involves understanding the three-dimensional conformation of the Rslcan-6 protein and identifying regions where small molecules can interact effectively. This design process often employs computational modeling and structural biology techniques such as X-ray crystallography or NMR spectroscopy. Once potential binding sites are identified, synthetic chemistry methods are employed to develop compounds that can selectively bind to these regions. The efficacy and potency of these inhibitors are assessed through biochemical assays that measure their binding affinity and their ability to modulate the activity of Rslcan-6 in vitro. Researchers continue to explore the fundamental mechanisms of how these inhibitors interact with Rslcan-6, contributing to a deeper understanding of intracellular signaling networks and the broader regulatory functions that proteins like Rslcan-6 perform within cellular environments.
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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 | |
A histone deacetylase inhibitor that can modulate gene expression by altering chromatin structure, potentially affecting ZNF457's transcriptional activity. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
A DNA methyltransferase inhibitor that changes DNA methylation patterns, which may indirectly impact ZNF457's gene regulatory functions. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Similar to Trichostatin A, this HDAC inhibitor can influence chromatin dynamics and gene expression, potentially affecting ZNF457 activity. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
Another DNA methyltransferase inhibitor that could alter methylation patterns affecting gene expression regulated by ZNF457. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Known to inhibit the proteasome and NF-kB pathway, it could indirectly influence ZNF457 through modulation of transcriptional regulation mechanisms. | ||||||
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 | |
A proteasome inhibitor that might affect the stability or function of transcription factors, including ZNF457, by influencing protein degradation. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
By inhibiting MEK, this compound could affect the MAPK/ERK pathway, potentially altering ZNF457's activity within these signaling contexts. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A PI3K inhibitor that may indirectly impact ZNF457's function by modulating the PI3K/AKT signaling pathway and its effects on transcriptional regulation. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
As a JNK inhibitor, it could affect transcription factors regulated by the JNK pathway, potentially including ZNF457. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Another PI3K inhibitor, potentially affecting ZNF457 by altering signaling pathways that influence transcription factor activity. | ||||||