EFP1 inhibitors are a class of chemical compounds designed to specifically target and modulate the activity of EFP1 (Estrogen-Responsive Finger Protein 1), a protein that functions as a transcription factor and is involved in regulating the expression of genes in response to hormonal signals, particularly estrogen. EFP1 is characterized by its zinc finger motifs, which allow it to bind to specific DNA sequences in the promoter regions of target genes. Upon binding to DNA, EFP1 influences the transcriptional activity of these genes, playing a crucial role in various cellular processes such as cell proliferation, differentiation, and the regulation of metabolic pathways. The activity of EFP1 is especially significant in tissues that are sensitive to estrogen, where it helps to mediate the cellular responses to hormonal changes.
Inhibitors of EFP1 work by interfering with its ability to bind to DNA or by disrupting its interactions with other proteins and cofactors that are necessary for its function as a transcription factor. These inhibitors may directly bind to the zinc finger domains of EFP1, preventing the protein from attaching to its target DNA sequences, thereby blocking the transcriptional regulation of estrogen-responsive genes. Alternatively, some inhibitors might affect the conformation of EFP1, altering its ability to interact with other transcriptional regulators or components of the transcriptional machinery. By inhibiting EFP1, these compounds provide researchers with tools to study the specific roles this protein plays in hormone-regulated gene expression and the broader regulatory networks that control cellular responses to hormonal signals. Investigating the effects of EFP1 inhibition can offer insights into the mechanisms of gene regulation in hormone-sensitive tissues and contribute to a deeper understanding of how hormonal signals influence cellular function and development.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Inhibits PI3K, a kinase upstream in many signaling pathways, which can regulate the activity of downstream proteins. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
Another PI3K inhibitor, which could suppress the activation of downstream signaling proteins like EFP1. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
Inhibits MEK, which is part of the MAPK/ERK pathway; potential modulation of EFP1 if it's a downstream effector. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
Inhibits p38 MAPK and could affect proteins regulated by p38 MAPK, including EFP1 if it's involved in this pathway. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits JNK, which might alter the activity of EFP1 if JNK is upstream in its signaling cascade. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Inhibits mTOR, which can impact the activity of downstream signaling proteins such as EFP1. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
Inhibits MEK1, which could influence EFP1 activity if EFP1 is a downstream target in the ERK signaling pathway. | ||||||
Triciribine | 35943-35-2 | sc-200661 sc-200661A | 1 mg 5 mg | $104.00 $141.00 | 14 | |
Inhibits AKT and can modulate the activity of proteins downstream of AKT, potentially including EFP1. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $94.00 $227.00 | 30 | |
Inhibits Src family kinases, which can alter downstream signaling pathways that may involve EFP1. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
Inhibits Src kinases and could modulate downstream signaling processes affecting EFP1. | ||||||