Gastrin Releasing Peptide (1-16), human

Gastrin Releasing Peptide (1-16), human

Gastrin Releasing Peptide (1-16), human

Gastrin Releasing Peptide (1-16), human

Gastrin Releasing Peptide (1-16), human

Gastrin Releasing Peptide (1-16), Human, often abbreviated as GRP(1-16), is a bioactive N-terminal fragment of the full-length 27-amino acid human Gastrin Releasing Peptide. This 16-amino acid peptide retains the core receptor-binding region and exhibits significant biological activity. It is widely recognized for its role as a neurotransmitter and mitogen, primarily functioning through the Gastrin Releasing Peptide Receptor (GRPR). 


TECHNICAL SPECIFICATIONS


Item
Specification
Product Name
Gastrin Releasing Peptide (1-16)
CAS NO.
/
Appearance
White to off-white lyophilized powder
Molecular Formula
C74H121N17O20S
Molecular Weight
1600.9g/mol 
Purity (RP-HPLC)
≥98.0%
Solubility

Soluble in water (≥10 mg/mL), dilute acetic acid, and DMSO

Endotoxin≤5.0 EU/mg
Biological Activity
 Potent agonist of the gastrin-releasing peptide receptor (GRPR)
Storage Conditions
Store at -20°C to -80°C in a sealed container, protected from moisture and light. 
Stock Location
Stock in USA
MOQ
1g


1.MECHANISM OF ACTION

GRP(1-16) exerts its effects by acting as a potent agonist for the Gastrin Releasing Peptide Receptor (GRPR, or BB2 receptor). This receptor is a G-protein coupled receptor (GPCR) primarily coupled to the Gq/11 protein. Upon binding, the peptide activates phospholipase C (PLC), leading to the hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP₂) into inositol trisphosphate (IP₃) and diacylglycerol (DAG). IP₃ triggers the release of calcium from intracellular stores, while DAG activates protein kinase C (PKC). 


    2.PRODUCT INDICATIONS

  • Receptor Signaling Studies: Investigating structure-activity relationships (SAR) of GRP, defining the minimal active sequence required for GRPR activation and downstream signaling.

  • Neurobiology Research: Studying the role of GRP fragments as neurotransmitters or neuromodulators in the central and peripheral nervous systems.

  • In VitroPharmacology: Serving as a reference agonist in GRPR binding assays (competitive displacement studies) and functional assays (calcium flux, IP₃ accumulation) to screen for antagonists or allosteric modulators.

  • Cancer Cell Biology: Exploring the mitogenic and proliferative effects of GRP fragments on GRPR-expressing cancer cell lines (e.g., small cell lung cancer, prostate cancer).

  • Peptide Analog Development: Used as a scaffold or benchmark in the design and testing of modified GRP analogs with improved stability or selectivity.

      

    3.CLINICAL EFFICACY OF PRODUCT

  • Research Validation: Preclinical studies confirm that this fragment retains significant biological activity in stimulating gastrin release and activating GRPR-mediated signaling pathways in vitro, though it may be less potent or stable in vivothan the full-length peptide.

  • Diagnostic/Therapeutic Prototype: While not a drug itself, research on this fragment contributes to understanding the GRP/GRPR system's role in disease. This knowledge underpins the development of GRPR-targeted diagnostics (e.g., radiolabeled ligands for PET imaging of tumors) and therapeutics (e.g., GRPR antagonists).

  • Clinical Translation Gap: No clinical trials have been conducted using GRP(1-16) as a therapeutic agent. Its clinical relevance is entirely indirect, serving as a tool to validate a drug target (GRPR) that is being actively investigated in oncology clinical trials.

  • Utility: Its primary value is in generating robust preclinical data to guide the development of future clinical candidates that modulate the GRP/GRPR axis.


  • 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.

Global Market Analysis and Oxandrolone 50mg Price Guide
Nov 05, 26
Global Market Analysis and Oxandrolone 50mg Price Guide
For B2B pharmaceutical buyers and researchers, understanding the oxandrolone 50mg price involves analyzing more than just a numerical value; it requires a comprehensive look at API purity, synthesis methods, and global supply chain stability. As a specialized anabolic steroid derivative, the cost is heavily influenced by the quality of raw materials and the rigor of the laboratory testing involved in the production process. This article explores the economic and technical variables that dictate market pricing for this specific compound. In the context of the global API market, pricing volatility is often tied to regulatory shifts in key manufacturing hubs
How to Select High Purity Alisol C CAS 30489271 for Laboratory Research
Nov 04, 26
How to Select High Purity Alisol C CAS 30489271 for Laboratory Research
High Purity Alisol C CAS 30489271 is suited to laboratories using Alisol C as a triterpenoid reference standard in metabolic, hepatology, pharmacology, HPLC/MS, botanical-extract, or selected cell-line research. We explain the application fit and the identity, purity, physical form, solvent, endotoxin, storage, quantity, and batch-record checks to make before ordering.
Reliable Oxandrolone Supplier for High Purity Pharmaceutical APIs
Nov 02, 26
Reliable Oxandrolone Supplier for High Purity Pharmaceutical APIs
When sourcing high-purity pharmaceutical ingredients for endocrine or cardiovascular research, the reliability of the supply chain is as critical as the chemical purity itself. For laboratories and manufacturers seeking a dependable oxandrolone supplier, the focus must extend beyond simple certificates of analysis to encompass consistent batch-to-batch stability and strict adherence to GMP standards. Whether the requirement is for small-scale pilot studies or large-scale industrial production, the ability to trace materials from raw synthesis to final lyophilized powder ensures the integrity of the resulting clinical or research data.

If you are interested in our products, you can choose to leave your information here, and we will be in touch with you shortly.