The chemical class of FRYL Inhibitors encompasses a diverse array of compounds, each distinct in structure but unified in their functional aim to modulate the activity of FRYL, a transcription coactivator involved in vital cellular processes such as gene regulation and chromatin remodeling. These inhibitors are not identified by a common chemical structure, but rather by their shared objective of influencing FRYL's role within the cell. The inhibitors in this class are designed to operate through various mechanisms, each tailored to disrupt or modify the integral processes of transcription regulation and chromatin dynamics in which FRYL is a key participant.
The primary mode of action for these inhibitors centers around the disruption of FRYL's interaction with the transcription machinery and its influence on chromatin structure. By targeting the interfaces where FRYL interacts with transcription factors or other coactivators, these compounds aim to impede the facilitation of transcription, a critical step in gene expression regulation. Additionally, some inhibitors in this class focus on altering the chromatin landscape itself, recognizing that transcription regulation is deeply intertwined with chromatin structure and accessibility. These compounds work by modifying the epigenetic marks or altering the physical structure of chromatin, thereby creating a cellular environment less conducive to FRYL's activity. This approach underscores the complex relationship between chromatin architecture and transcription regulation, highlighting the intricate nature of targeting proteins like FRYL that operate within these dynamic structures. The exploration of FRYL Inhibitors represents an advanced field within molecular biology, emphasizing the modulation of key proteins involved in transcription regulation. By delving into the potential of targeted molecular interventions, this class of inhibitors not only enriches our fundamental understanding of transcription and chromatin dynamics but also exemplifies the nuanced approach required to influence specific protein functions within complex biological systems. The development and study of these inhibitors showcase the potential of precise molecular targeting in elucidating the roles of specific proteins like FRYL in transcription regulation.
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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 | |
Inhibits histone deacetylases, increasing histone acetylation and potentially altering chromatin structure, which can indirectly impact FRYL's transcription coactivator function. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
Acts as a DNA methyltransferase inhibitor, reducing DNA methylation and potentially affecting chromatin remodeling, which might indirectly influence FRYL's function in gene regulation. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Another histone deacetylase inhibitor, Suberoylanilide Hydroxamic Acid can modify chromatin accessibility, which might influence FRYL's role in transcription regulation. | ||||||
GDC-0941 | 957054-30-7 | sc-364498 sc-364498A | 5 mg 10 mg | $184.00 $195.00 | 2 | |
Inhibits histone methyltransferases, altering histone methylation patterns and potentially impacting FRYL's involvement in chromatin structure and gene expression. | ||||||
C646 | 328968-36-1 | sc-364452 sc-364452A | 10 mg 50 mg | $260.00 $925.00 | 5 | |
Selectively inhibits histone acetyltransferase p300, potentially affecting chromatin acetylation and structure, thereby impacting FRYL's transcriptional coactivator activity. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
Inhibits RNA polymerase II, reducing overall transcription levels and indirectly affecting FRYL's coactivator functions. | ||||||
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | $206.00 $299.00 $485.00 | 10 | |
A PARP inhibitor, Olaparib might indirectly affect chromatin dynamics, thereby influencing FRYL's role in transcription regulation. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $196.00 | 9 | |
A broad-spectrum histone deacetylase inhibitor, Panobinostat could indirectly influence chromatin remodeling activities and FRYL's function. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
As a histone deacetylase inhibitor, MS-275 can impact chromatin structure, potentially influencing FRYL's role in transcription regulation. | ||||||
JNJ-26481585 | 875320-29-9 | sc-364515 sc-364515A | 5 mg 50 mg | $321.00 $1224.00 | ||
Another histone deacetylase inhibitor, JNJ-26481585 could affect chromatin structure, potentially impacting FRYL's transcription regulatory function. | ||||||