FEZ1 activators constitute a group of chemical agents designed to modulate the activity of the Fasciculation and Elongation Protein Zeta-1 (FEZ1), which is implicated in neuronal development and cellular transport processes. FEZ1 has been found to play a role in axonal outgrowth and the transport of materials along the axon, which are critical for the proper functioning and development of neurons.
Direct FEZ1 activators would interact with the protein at a molecular level, potentially binding to its active site or a regulatory domain, thereby inducing a conformational change that enhances the protein's ability to interact with its partners, such as kinesin motor proteins. This could lead to an increased efficiency in intracellular transport mechanisms, particularly in neurons, where FEZ1 is known to be involved in the transport of neurotrophic factors and synaptic vesicle precursors. Indirect activators of FEZ1 might not bind to the protein itself but could influence its activity by modulating the expression of the FEZ1 gene, thereby increasing protein synthesis. Alternatively, they might inhibit the degradation pathways of the protein, leading to a higher steady-state level of FEZ1 in the cell. Indirect activators could also affect the post-translational modifications of FEZ1, such as phosphorylation, which are known to regulate its activity and interactions with other proteins involved in the transport processes.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA is a potent activator of Protein Kinase C (PKC), which can interact with FEZ1. By activating PKC, PMA can indirectly influence FEZ1 activity. | ||||||
Bisindolylmaleimide I (GF 109203X) | 133052-90-1 | sc-24003A sc-24003 | 1 mg 5 mg | $103.00 $237.00 | 36 | |
Bisindolylmaleimide I is a potent and selective inhibitor of PKC. By modulating PKC activity, it can indirectly influence the function of FEZ1. | ||||||
Gö 6976 | 136194-77-9 | sc-221684 | 500 µg | $223.00 | 8 | |
Go 6976 is a selective PKC inhibitor, particularly PKCα and PKCβ. It can indirectly influence FEZ1 through the modulation of PKC. | ||||||
Gö 6983 | 133053-19-7 | sc-203432 sc-203432A sc-203432B | 1 mg 5 mg 10 mg | $103.00 $293.00 $465.00 | 15 | |
Gö 6983 is an inhibitor of PKC. It can potentially influence FEZ1 by modulating PKC activity. | ||||||
4-Nitrobenzaldehyde | 555-16-8 | sc-256809 | 10 g | $41.00 | ||
Neurotensin is a neuropeptide that can activate NTSR1, which is known to interact with FEZ1. Therefore, it can indirectly modulate FEZ1. | ||||||
SR 48692 | 146362-70-1 | sc-363290 sc-363290A sc-363290B sc-363290C sc-363290D | 5 mg 25 mg 100 mg 500 mg 1 g | $156.00 $593.00 $2327.00 $10500.00 $20990.00 | 2 | |
SR 48692 is another antagonist of NTSR1. It can potentially affect FEZ1 by modulating NTSR1. | ||||||
Vinblastine | 865-21-4 | sc-491749 sc-491749A sc-491749B sc-491749C sc-491749D | 10 mg 50 mg 100 mg 500 mg 1 g | $100.00 $230.00 $450.00 $1715.00 $2900.00 | 4 | |
Vinblastine, similar to Vincristine, is a microtubule-disrupting drug. It can potentially affect FEZ1 by modulating the microtubule network. | ||||||
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $40.00 $73.00 $217.00 $242.00 $724.00 $1196.00 | 39 | |
Paclitaxel is a microtubule-stabilizing drug that can indirectly influence FEZ1 by affecting the microtubule network. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $58.00 $83.00 $140.00 $242.00 | 38 | |
Nocodazole is a microtubule-disrupting drug. It can potentially influence FEZ1 by modulating the microtubule network. | ||||||
Colchicine | 64-86-8 | sc-203005 sc-203005A sc-203005B sc-203005C sc-203005D sc-203005E | 1 g 5 g 50 g 100 g 500 g 1 kg | $98.00 $315.00 $2244.00 $4396.00 $17850.00 $34068.00 | 3 | |
Colchicine is another microtubule-disrupting drug. It can indirectly influence FEZ1 by affecting the microtubule network. | ||||||