neuropeptide s

Neuropeptide S human (TFA) is a potent endogenous neuropeptide S receptor agonist (EC50=9.4 nM).

Potent endogenous neuropeptide S receptor (NPSR) agonist (EC50 = 3 nM). Induces mobilization of intracellular Ca2+. Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.

Potent endogenous neuropeptide S receptor (NSPR) agonist (EC50 = 3.2 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.

Potent endogenous neuropeptide S receptor agonist (EC50 = 9.4 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.

Neuropeptide S (Rat) acetate is an endogenous ligand of a previously orphan G-protein-coupled receptor now named NPS receptor. Neuropeptide S (Rat) acetate can be used for the research of nervous system disease [1].

Neuropeptide S(Mouse) TFA, an endogenous agonist for the neuropeptide S receptor (NPSR) with an EC50 value of 3 nM, plays a significant role in physiological processes by inducing the mobilization of intracellular Ca2+. This compound elevates locomotor activity and wakefulness, and simultaneously decreases anxiety-like behavior in mice.

Neuropeptide S(Rat) TFA, a robust endogenous agonist for the neuropeptide S receptor (NSPR) with an EC50 of 3.2 nM, enhances locomotor activity and promotes wakefulness while concurrently diminishing anxiety-like behavior in mice.

Neuropeptide S (Mouse) acetate is a bioactive peptide. Neuropeptide S (Mouse) acetate, as a neurotransmitter/neuromodulator of 20 amino acids, can be used for the research of arousal, anxiety, locomotion, feeding behaviors, memory and drug addiction[1].

Neuropeptide SF(mouse,rat) acetate (Neuropeptide SF(mouse,rat) acetate (230960-31-3 free base)) is a potent neuropeptide FF receptor agonist, Ki for NPFF1 and NPFF2 are 48.4 nM and 12.1 nM, respectively. Neuropeptide SF(mouse,rat) acetate (Neuropeptide SF(mouse,rat) acetate (230960-31-3 free base)) increases the amplitude of the sustained current of heterologously expressed acid sensing ion channel 3 (ASIC3).

Neuropeptide S (human)-13C2,15N is a 13C and 15N labeled version of Neuropeptide S (human). This neuropeptide is a potent agonist of the homologous neuropeptide S receptors (NPSR). Neuropeptide S human is utilized in research concerning Alzheimer's disease (AD).

Neuropeptide SF (human) considerably increases the amplitude of the sustained current of heterologously expressed ASIC3 (12-fold vs. 19- and nine-fold for FMRFamide and NPFF, respectively) with an EC50 of ~50 μM.

Neuropeptide SF (human) acetate is a neuropeptide that augmented paraventricular CRH release and increased ACTH and corticosterone levels in the plasma.

Neuropeptide SF (mouse, rat) TFA, a potent agonist for neuropeptide FF receptors, exhibits K_i values of 48.4 nM for NPFF1 and 12.1 nM for NPFF2. Additionally, this compound enhances the amplitude of the sustained current in heterologously expressed acid-sensing ion channel 3 (ASIC3) [1].

neuropeptide S receptor (NPSR) antagonist

Salmfamide 1 is a neuropeptide.

(S)-VU0637120 is a selective neuropeptide Y(4)R-mutant antagonist used in the study of metabolic disorders.

SHA 68 is a potent and selective non-peptide antagonist of neuropeptide S receptor (NPSR) with IC50 values of 22.0 nM for NPSR Asn107 and 23.8 nM for NPSR Ile107.

Velneperit (S2367) is potent and selective neuropeptide Y (NPY) Y5 receptor under evaluating for treatment of obesity.

NPSR1 antagonist-1 is a potent and peripherally restricted antagonist of the neuropeptide S receptor 1 (NPSR1). It can inhibit the expression of IL-6, PTGS2, IL-20, and CXCL8, and it also reduces TNF-α cytokine levels. NPSR1 antagonist-1 is useful in inflammation-related research, such as peritonitis studies.

R06039-696 is a neuropeptide S receptor (NPSR) agonist with an EC50 of 91 nM. It plays a role in regulating various biological functions such as wakefulness, stress and anxiety responses, memory processes, and food intake by activating the neuropeptide S receptor.

R06039-636 is a neuropeptide S receptor (NPSR) agonist with an EC50 value of 94 nM.

R06039-641 is an agonist of the neuropeptide S receptor (NPSR) with an EC50 of 169 nM. By activating this receptor, R06039-641 plays a role in modulating various biological functions, including arousal, stress and anxiety responses, memory processes, and food intake.

R06039-691 is a neuropeptide S receptor (NPSR) agonist with an EC50 of 93 nM. It participates in the regulation of various biological functions, such as wakefulness, stress and anxiety responses, memory processes, and food intake, through the activation of neuropeptide S receptors.

R06039-641 is a neuropeptide S receptor (NPSR) agonist with an EC50 of 169 nM. It participates in regulating various biological functions such as arousal, stress and anxiety responses, memory processes, and food intake by activating the neuropeptide S receptor.