The let-23 activators constitute a class of chemicals that exert their effects by modulating the activity of the let-23 protein, a receptor tyrosine-protein kinase. This class primarily consists of compounds that influence the epidermal growth factor (EGF) receptor pathway, which is intrinsically linked to let-23 function. These molecules encompass growth factors that specifically bind and activate EGF receptors, including let-23. Upon ligand binding, let-23 undergoes dimerization and autophosphorylation, initiating a cascade of intracellular signaling events.
Additionally, there are specific tyrosine kinase, including AG 1478, Gefitinib, Lapatinib, Erlotinib, and PD153035. Intriguingly, while primarily of the EGFR pathway, under certain cellular contexts, these compounds can paradoxically enhance EGFR phosphorylation or promote receptor dimerization. This results in heightened signaling through the EGFR pathway, subsequently influencing let-23 activity. Furthermore, compounds like Anandamide, Arsenite, and Selenite showcase the diversity in let-23 modulators. Anandamide, an endocannabinoid, demonstrates the capability to activate the EGFR pathway, thereby indirectly influencing let-23. Meanwhile, Arsenite and Selenite function by modulating the cellular oxidative environment, which can be conducive for the activation of the EGFR pathway and consequently, let-23. Together, these compounds elucidate the multifaceted nature of let-23 regulation, reflecting its critical role in diverse cellular processes and emphasizing the intricacies of targeting such a pivotal protein.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $63.00 $114.00 $218.00 $349.00 | 74 | |
EGFR tyrosine kinase inhibitor which paradoxically can enhance EGFR phosphorylation under specific conditions, thereby increasing let-23 signaling. | ||||||
Lapatinib | 231277-92-2 | sc-353658 | 100 mg | $420.00 | 32 | |
Dual tyrosine kinase inhibitor that targets both EGFR and HER2. In certain contexts, it can lead to enhanced EGFR pathway signaling, indirectly influencing let-23 activity. | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $87.00 $135.00 $293.00 $505.00 $3827.00 | 42 | |
EGFR inhibitor that can, under certain circumstances, promote receptor dimerization and subsequent signaling, indirectly modulating let-23 activity. | ||||||
Sodium (meta)arsenite | 7784-46-5 | sc-250986 sc-250986A | 100 g 1 kg | $108.00 $780.00 | 3 | |
Can lead to the activation of the EGFR pathway by enhancing the oxidative environment. This results in let-23 activation and subsequent cellular responses. | ||||||
Sodium selenite | 10102-18-8 | sc-253595 sc-253595B sc-253595C sc-253595A | 5 g 500 g 1 kg 100 g | $49.00 $183.00 $316.00 $98.00 | 3 | |
Enhances EGFR pathway activity in certain contexts by modifying the cellular oxidative state. This can lead to increased let-23 activity. | ||||||
PD 153035 | 153436-54-5 | sc-205909 | 5 mg | $146.00 | 5 | |
EGFR-specific inhibitor which in certain conditions might promote receptor signaling, indirectly modulating let-23 activity. | ||||||