[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat

[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat

[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat

[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat

[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat

[D-Arg²⁵]-Neuropeptide Y, human, rat is a metabolically stabilized analog of native NPY with a D-arginine substitution at position 25, supplied as a lyophilized powder with ≥95% HPLC purity and low endotoxin levels. This research-grade peptide retains high affinity for multiple NPY receptor subtypes (Y₁, Y₂, Y₄, Y₅) while exhibiting enhanced proteolytic stability compared to native NPY, making it a valuable tool for prolonged in vitroand in vivostudies of NPY signaling. It is widely used in receptor binding assays, functional studies of cAMP inhibition, and investigations into feeding behavior, energy homeostasis, anxiety, and cardiovascular regulation where sustained NPY receptor activation is required.



TECHNICAL SPECIFICATIONS


Item
Specification
Product Name
[D-Arg25]-Neuropeptide Y, human, rat; [D-Arg25]-NPY, human, rat
CAS NO.
/
Appearance
White to off-white lyophilized powder
Molecular Formula
 C189H285N55O57S
Molecular Weight
 4271.8g/mol 
Purity (RP-HPLC)
≥ 95.0%
Solubility

Soluble in water, dilute acetic acid (e.g., 0.1 % v/v), or phosphate‑buffered saline (PBS). For best results, first dissolve in a small volume of 0.1 % acetic acid or sterile water to prepare a 0.1–1.0 mg/mL stock solution.

Endotoxin< 1.0 EU/mg
Biological Activity
This analog contains a D‑arginine substitution at position 25, which is intended to enhance metabolic stability against proteolytic degradation while largely preserving receptor binding affinity for NPY receptors (Y₁, Y₂, Y₄, Y₅). It acts as an agonist, inhibiting adenylate cyclase via Gi/o protein coupling. Bioactivity should be validated in NPY receptor binding or functional assays (e.g., cAMP inhibition).
Storage Conditions
Lyophilized powder: Store desiccated at –20 °C or below, protected from light, for long‑term stability.
Reconstituted solution: Aliquot and store at ≤ –20 °C; avoid repeated freeze‑thaw cycles. For extended stability, store at –80 °C.
Stock Location
Stock in USA
MOQ
1g


1.MECHANISM OF ACTION

[D-Arg²⁵]-NPY functions as a broad-spectrum NPY receptor agonist, binding to Y₁, Y₂, Y₄, and Y₅ receptors with high affinity and coupling to Gi/o proteins to inhibit adenylate cyclase, leading to reduced intracellular cAMP levels. This signaling cascade activates inwardly rectifying potassium channels and inhibits voltage-gated calcium channels, resulting in neuronal hyperpolarization, decreased neurotransmitter release, and modulation of various physiological processes. The D-arginine substitution at position 25 enhances resistance to proteolytic degradation by endopeptidases, prolonging the peptide's half-life and duration of action without significantly altering receptor binding properties, thereby providing sustained activation of NPY receptor pathways.


2.PRODUCT INDICATIONS

This metabolically stabilized NPY analog is indicated exclusively for research applications requiring prolonged NPY receptor activation. It is employed in NPY receptor binding and autoradiography studies across multiple subtypes, functional assays measuring sustained cAMP inhibition and calcium signaling, feeding behavior and energy homeostasis research with extended duration of effect, anxiety and stress response models requiring chronic NPY exposure, cardiovascular function studies investigating prolonged vasoconstriction and blood pressure modulation, and validation of NPY receptor expression and signaling in various tissues. The product serves as a reference agonist for screening NPY receptor antagonists and studying the role of sustained NPY signaling in obesity, metabolic disorders, anxiety, and cardiovascular diseases. It is not intended for diagnostic, therapeutic, or clinical use.


3.CLINICAL EFFICACY OF PRODUCT

As a research reagent, [D-Arg²⁵]-Neuropeptide Y, human, rat has no established clinical efficacy or safety profile for therapeutic applications. The peptide has not undergone clinical trials, regulatory approval, or safety evaluation for any medical indication. While it contributes to fundamental understanding of NPY receptor biology and may inform the development of future therapeutic agents targeting NPY receptors for obesity, metabolic disorders, anxiety, or cardiovascular conditions, its utility remains confined to preclinical research. Any clinical translation would require development of entirely distinct therapeutic agents with comprehensive preclinical and clinical testing.


4.DELIVERY & SHIPPING

We specialize in global logistics for various cosmetic peptides. Your order will be handled with the utmost care, ensuring safe, reliable, and intact delivery.
Professional and Secure Packaging
Each bottle of peptide is protected with a special packaging solution to ensure stability and integrity during transportation.
We can also customize packaging according to customer needs.
Shipping Methods 
Main Method: International Air Freight

We primarily use DHL, FedEx, UPS, and TNT because of their global reliability, speed, and advanced tracking systems. Air freight ensures the fastest transit time and minimizes the impact of environmental factors on the product.

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