Gros1 inhibitors belong to a class of chemical compounds that are designed to target and modulate the activity of the Gros1 protein. Gros1, also known as Growth Factor Receptor-Bound Protein 10 (Grb10)-interacting GYF protein 2 (GIGYF2), is a critical player in cellular signaling pathways. It is involved in regulating the insulin and insulin-like growth factor 1 (IGF-1) signaling pathways, which are essential for controlling glucose metabolism and cell growth. Gros1 functions as an adaptor protein, facilitating the interaction between various signaling molecules. In normal physiological conditions, Gros1 acts as a negative regulator of these pathways by inhibiting the activation of downstream signaling molecules. However, dysregulation of Gros1 can lead to aberrant signaling and is implicated in various disease processes.
Gros1 inhibitors are designed to selectively target Gros1 and modulate its activity. These inhibitors can function through various mechanisms, including disrupting protein-protein interactions involving Gros1 or interfering with its phosphorylation and subsequent signaling cascade activation. By inhibiting Gros1, these compounds have the potential to fine-tune insulin and IGF-1 signaling pathways, which could have implications in various cellular processes. Researchers are actively investigating the use of Gros1 inhibitors as tools for understanding the intricate mechanisms underlying metabolic and growth-related disorders.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $256.00 | 18 | |
Tamoxifen is a selective estrogen receptor modulator (SERM) that competes with estrogen for binding to estrogen receptors, indirectly inhibiting Gros1 through estrogen receptor modulation. | ||||||
ICI 182,780 | 129453-61-8 | sc-203435 sc-203435A | 1 mg 10 mg | $81.00 $183.00 | 34 | |
Fulvestrant is a SERM that acts as an estrogen receptor antagonist. It binds to estrogen receptors and promotes their degradation, blocking estrogen signaling and inhibiting Gros1. | ||||||
Anastrozole | 120511-73-1 | sc-217647 | 10 mg | $90.00 | 1 | |
Anastrozole is an aromatase inhibitor that reduces estrogen production, indirectly affecting Gros1 through lower estrogen levels. | ||||||
Letrozole | 112809-51-5 | sc-204791 sc-204791A | 25 mg 50 mg | $85.00 $144.00 | 5 | |
Letrozole is another aromatase inhibitor that lowers estrogen synthesis, indirectly impacting Gros1 through reduced estrogen signaling. | ||||||
Raloxifene | 84449-90-1 | sc-476458 | 1 g | $802.00 | 3 | |
Raloxifene is a SERM that modulates estrogen receptors, indirectly influencing Gros1 activity through its regulation of estrogen receptor activity. | ||||||
Exemestane | 107868-30-4 | sc-203045 sc-203045A | 25 mg 100 mg | $131.00 $403.00 | ||
Exemestane is an aromatase inhibitor that reduces estrogen synthesis, indirectly impacting Gros1 by lowering estrogen levels. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $315.00 | ||
Palbociclib is a CDK inhibitor that indirectly affects Gros1 by inhibiting cell cycle progression, which is linked to Gros1 activity. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $128.00 $638.00 | 7 | |
Everolimus is an mTOR inhibitor that indirectly impacts Gros1 by disrupting cell growth and proliferation pathways. | ||||||