NETO2 inhibitors belong to a class of chemical compounds designed to target and modulate the activity of NETO2, which stands for Neuropilin and Tolloid-like 2 protein. NETO2 is a protein that has been primarily studied in the context of synaptic function within the nervous system. It is known to interact with and modulate the activity of ionotropic glutamate receptors, particularly AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) receptors. These receptors are critical for mediating fast excitatory neurotransmission in the brain. NETO2's association with AMPA receptors suggests a role in regulating synaptic strength and plasticity, which are essential for learning and memory processes. Inhibitors developed to target NETO2 are primarily employed in molecular and cellular biology research to investigate the functional properties and regulatory mechanisms associated with this protein.
The development of NETO2 inhibitors typically involves a combination of biochemical, biophysical, and structural approaches aimed at identifying or designing molecules that can selectively interact with NETO2 and modulate its activity. By inhibiting NETO2, these compounds can disrupt the regulation of AMPA receptors, affecting synaptic transmission and plasticity. Researchers use NETO2 inhibitors to explore the intricate roles played by this protein in neuronal functions, attempting to unravel its contributions to synaptic modulation, neuronal excitability, and interactions with other synaptic proteins and pathways. Furthermore, these inhibitors serve as valuable tools for dissecting the broader network of cellular processes involving glutamate receptors and their regulatory roles in synaptic plasticity, contributing to our understanding of fundamental neuroscience mechanisms and providing insights into avenues for further scientific exploration.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $74.00 $243.00 $731.00 $2572.00 $21848.00 | 53 | |
Binds to DNA and inhibits RNA synthesis, potentially reducing NETO2 mRNA levels and protein expression. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
Inhibits eukaryotic protein synthesis, likely reducing NETO2 protein levels by preventing its translation. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $269.00 $1050.00 | 26 | |
Inhibitor of RNA polymerase II, potentially reducing NETO2 mRNA synthesis and subsequent protein expression. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $58.00 $186.00 $94.00 | 21 | |
Inhibits DNA topoisomerase I, leading to reduced DNA replication and potentially lower NETO2 expression. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $51.00 $231.00 $523.00 | 63 | |
Inhibits DNA topoisomerase II, which can lead to decreased replication and transcription, possibly affecting NETO2 levels. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $66.00 $101.00 $143.00 | 85 | |
Alkylates DNA and can inhibit DNA synthesis, potentially reducing the expression of NETO2. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Diterpene triepoxide that inhibits the transcription of a wide range of genes, potentially including NETO2. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
Proteasome inhibitor that can affect protein turnover and may indirectly decrease NETO2 protein levels. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $69.00 | 2 | |
Known to inhibit DNA and RNA synthesis at high concentrations, which could reduce NETO2 expression. | ||||||
Rocaglamide | 84573-16-0 | sc-203241 sc-203241A sc-203241B sc-203241C sc-203241D | 100 µg 1 mg 5 mg 10 mg 25 mg | $275.00 $474.00 $1639.00 $2497.00 $5344.00 | 4 | |
Inhibits eukaryotic translation initiation, potentially decreasing NETO2 protein synthesis. | ||||||