Neuropeptide S inhibitors represent a class of chemical compounds that specifically target neuropeptide S (NPS), a neuropeptide implicated in various physiological and behavioral processes. Neuropeptide S is primarily produced in the brain and has been shown to influence a range of functions including anxiety, arousal, and the regulation of stress responses. It exerts its effects by binding to its specific receptor, NPSR (neuropeptide S receptor), which is a G protein-coupled receptor (GPCR). This binding activates intracellular signaling pathways that can modulate neuronal excitability and influence various behavioral responses, particularly those related to anxiety and stress management.
The development of neuropeptide S inhibitors is rooted in a detailed understanding of the structural and functional characteristics of the NPS-NPSR interaction. Researchers often utilize high-throughput screening techniques to identify small molecules that can effectively bind to the NPS receptor and inhibit its activity. By analyzing the structure of the neuropeptide and its receptor, scientists can design inhibitors that mimic or block the action of neuropeptide S, disrupting the receptor's ability to activate signaling pathways. This modulation of neuropeptide S activity provides valuable insights into the underlying mechanisms of stress and anxiety, contributing to a more comprehensive understanding of how neuropeptides regulate behavior and physiological responses. The ongoing research in this field continues to elucidate the role of neuropeptide S in various biological processes and enhances our knowledge of neuropeptide signaling dynamics.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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SQ 22536 | 17318-31-9 | sc-201572 sc-201572A | 5 mg 25 mg | $93.00 $356.00 | 13 | |
Adenylate cyclase inhibitor that reduces cAMP production. If AC activity is reduced, the signal from NPS binding to its receptor is blunted. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $75.00 $212.00 | 18 | |
Phosphodiesterase 4 (PDE4) inhibitor. PDE4 breaks down cAMP. By inhibiting PDE4, cAMP is elevated, potentially causing desensitization to NPS signaling. | ||||||
KT 5720 | 108068-98-0 | sc-3538 sc-3538A sc-3538B | 50 µg 100 µg 500 µg | $97.00 $144.00 $648.00 | 47 | |
Another PKA inhibitor that can blunt the downstream effects of elevated cAMP caused by NPS activation. | ||||||
ML-9 | 105637-50-1 | sc-200519 sc-200519A sc-200519B sc-200519C | 10 mg 50 mg 100 mg 250 mg | $110.00 $440.00 $660.00 $1200.00 | 2 | |
Inhibits adenylate cyclase thereby limiting the production of cAMP. Reduced cAMP production can affect NPS signaling. | ||||||
Somatostatin | 51110-01-1 | sc-391009 sc-391009A | 1 mg 5 mg | $112.00 $525.00 | 9 | |
Cyclic AMP analog that acts as a competitive antagonist at cAMP-dependent pathways. It competes with cAMP and can thereby modulate NPS signaling. | ||||||
ZM 241385 | 139180-30-6 | sc-361421 sc-361421A | 5 mg 25 mg | $90.00 $349.00 | 1 | |
Adenosine A2A receptor antagonist. This receptor can modulate adenylate cyclase activity, and its antagonism can indirectly modulate NPS signaling. | ||||||
SCH 442416 | 316173-57-6 | sc-204271 sc-204271A | 1 mg 10 mg | $95.00 $245.00 | 3 | |
Adenosine A2A receptor antagonist that can modulate cAMP levels and potentially influence NPS signaling. |