FKHRL1, also known as FOXO3 or forkhead box O3, is a member of the FOXO family of transcription factors. These proteins possess a distinct DNA-binding domain known as the "forkhead box" or "winged helix" domain, which allows them to bind to specific DNA sequences and regulate the transcription of target genes. FOXO3 plays a critical role in various cellular processes, including cell cycle regulation, apoptosis, oxidative stress response, and DNA repair. Activation or deactivation of FOXO3 is often mediated through post-translational modifications, such as phosphorylation, acetylation, and ubiquitination. For instance, in response to certain growth factors, FOXO3 can be phosphorylated by the protein kinase AKT, leading to its exclusion from the nucleus and subsequent degradation. Given its central role in cellular homeostasis and response to environmental cues, the precise regulation of FOXO3 is of paramount importance. Dysregulation of its activity can disturb cellular functions and contribute to a range of anomalies.
FKHRL1 inhibitors, referring to compounds that target FOXO3, are a class of molecules designed to modulate the activity of this transcription factor. These inhibitors might function by directly interfering with the DNA-binding capability of FOXO3, preventing it from regulating target gene expression. Alternatively, they could modulate the post-translational modifications of FOXO3, influencing its localization, stability, or interaction with other proteins. Some inhibitors might also disrupt the interaction between FOXO3 and its coactivators or corepressors, altering its transcriptional activity.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
GSK 690693 | 937174-76-0 | sc-363280 sc-363280A | 10 mg 50 mg | $255.00 $1071.00 | 4 | |
GSK690693 is an AKT inhibitor. By inhibiting AKT, it indirectly promotes the activation and nuclear retention of FKHRL1. However, it can affect other pathways that down-regulate FKHRL1. | ||||||
Triciribine | 35943-35-2 | sc-200661 sc-200661A | 1 mg 5 mg | $104.00 $141.00 | 14 | |
Triciribine is a specific AKT inhibitor. While it primarily blocks AKT, it might have effects on other pathways influencing FKHRL1 levels. | ||||||
AZD5363 | 1143532-39-1 | sc-503190 | 5 mg | $309.00 | ||
AZD5363 is a potent inhibitor of AKT. Its inhibition of AKT can influence the phosphorylation status of FKHRL1. | ||||||
MK-2206 dihydrochloride | 1032350-13-2 | sc-364537 sc-364537A | 5 mg 10 mg | $182.00 $332.00 | 67 | |
MK-2206 is another AKT inhibitor, which might down-regulate FKHRL1 by affecting its phosphorylation status. | ||||||
Perifosine | 157716-52-4 | sc-364571 sc-364571A | 5 mg 10 mg | $188.00 $327.00 | 1 | |
Perifosine is an alkylphospholipid AKT inhibitor. Its role in down-regulating FKHRL1 is linked to its effect on AKT signaling. | ||||||
2-Amino-6-chloro-α-cyano-3-(ethoxycarbonyl)-4H-1-benzopyran-4-acetic Acid Ethyl Ester | 305834-79-1 | sc-479756 | 25 mg | $380.00 | ||
2-Amino-6-chloro-α-cyano-3-(ethoxycarbonyl)-4H-1-benzopyran-4-acetic Acid Ethyl Ester is a unique AKT activator. Activation of AKT can lead to the phosphorylation and inactivation of FKHRL1. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits mTOR, which can influence AKT signaling. This might have downstream effects on FKHRL1 phosphorylation. | ||||||
BEZ235 | 915019-65-7 | sc-364429 | 50 mg | $211.00 | 8 | |
NVP-BEZ235 is a dual PI3K/mTOR inhibitor. By affecting these pathways, it can influence the activity and levels of FKHRL1. | ||||||