GLP-001-S

$350.00$1,220.00

Semaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist studied extensively for its effects on glucose regulation and appetite signaling pathways. As a synthetic analog of human GLP-1, it mimics the hormone’s action by binding to and activating GLP-1 receptors, which play a key role in metabolic regulation. Semaglutide’s enhanced resistance to enzymatic degradation allows for extended activity in vivo, making it a preferred compound in metabolic research.

In laboratory settings, Semaglutide has been used to study mechanisms of insulin secretion, appetite suppression, and delayed gastric emptying. Its properties have also made it a key molecule in preclinical models examining obesity and metabolic syndrome. Due to its strong affinity for the GLP-1 receptor, Semaglutide has demonstrated robust effects on reducing food intake and improving metabolic parameters in animal models.

Researchers continue to explore Semaglutide in studies related to body weight regulation, energy expenditure, and glucose homeostasis. It remains a critical compound for scientists investigating pathways associated with type 2 diabetes, obesity, and gastrointestinal motility.

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Description

Semaglutide is a long-acting synthetic analog of glucagon-like peptide-1 (GLP-1), a naturally occurring incretin hormone responsible for enhancing glucose-dependent insulin secretion. It was developed through amino acid substitutions that significantly improve its resistance to dipeptidyl peptidase-4 (DPP-4) degradation, giving it a prolonged half-life and enabling once-weekly administration in clinical settings.

In scientific research, Semaglutide is studied for its potential to regulate glucose metabolism and body weight through various mechanisms. Upon activation of the GLP-1 receptor, Semaglutide stimulates insulin secretion, inhibits glucagon release, delays gastric emptying, and promotes satiety through central nervous system pathways. These effects make it a valuable compound in research involving energy balance and glycemic control.

One of the distinguishing features of Semaglutide is its ability to cross the blood-brain barrier and act directly on appetite-regulating regions in the hypothalamus. In animal models, this interaction has led to a notable reduction in food intake and an increase in weight loss, independent of caloric intake changes.

Research also suggests that Semaglutide may influence lipid metabolism, inflammatory cytokine expression, and cardiovascular parameters. In models of metabolic dysfunction, the peptide has demonstrated improvements in insulin sensitivity, hepatic steatosis, and systemic inflammation.

Beyond metabolism, Semaglutide is being explored for its neuroprotective properties. Studies are examining its potential to protect neurons from oxidative stress, improve memory function, and influence neuroinflammatory processes. These findings may broaden its application in research on cognitive decline and neurodegenerative disorders.

The compound’s extended half-life and high receptor selectivity make it a preferred choice for studying long-term metabolic adaptations in rodent and primate models. It enables consistent receptor activation over time, which is essential in chronic studies exploring the progression or mitigation of metabolic conditions.

Importantly, all research involving Semaglutide must remain within the bounds of non-clinical use. While promising, its regulatory status restricts use to laboratory environments focused on scientific exploration.

Note: This peptide is not intended for human consumption or clinical use. It is for research purposes only.

Product Data:

  • Chemical Name: Semaglutide (GLP-1 Analog)
  • CAS Number: 910463-68-2
  • Molecular Formula: C187H291N45O59
  • Molecular Weight: 4113.58 g/mol

Research

Semaglutide has become a focal point in metabolic research due to its robust pharmacological profile and extended activity. As a GLP-1 receptor agonist, it mimics the action of endogenous GLP-1, a peptide secreted by intestinal L-cells in response to food intake. GLP-1 plays a crucial role in regulating postprandial glucose levels and promoting satiety, making its analogs ideal candidates for obesity and diabetes research.

In rodent models, Semaglutide has demonstrated consistent glycemic control, driven by its stimulation of insulin release and suppression of glucagon secretion. Its effects on gastric motility slow nutrient absorption, contributing to its glucose-lowering action. These characteristics make Semaglutide a useful tool in studies focused on the interplay between gastrointestinal signaling and systemic metabolism.

Beyond glucose control, research has shown that Semaglutide significantly reduces food intake and body weight in diet-induced obese mice and non-human primates. The peptide activates anorexigenic neurons in the hypothalamus, including POMC and CART-expressing neurons, while inhibiting orexigenic pathways. This mechanism has led to extensive exploration of Semaglutide in appetite regulation and energy expenditure models.

Cardiometabolic research using Semaglutide has highlighted improvements in lipid profiles, inflammatory markers, and endothelial function. These findings support its use in studying the complex relationship between metabolic disease and cardiovascular risk.

Additional research has begun to examine Semaglutide’s potential neuroprotective and cognitive effects. In models of neurodegeneration, it has been observed to reduce oxidative damage and improve memory-related tasks. These results suggest GLP-1 analogs may hold promise in neurological applications, although more research is necessary to clarify their mechanisms.

Recent investigations have also looked into Semaglutide’s potential in hepatic and renal models. Animal studies indicate reductions in hepatic fat accumulation and improved kidney function under metabolic stress, providing further support for the peptide's systemic effects.

Collectively, Semaglutide serves as a powerful model compound in metabolic and endocrine research. Its stability, efficacy, and wide range of systemic actions make it ideal for long-term experimental designs aimed at uncovering the intricacies of metabolic regulation.

This material is provided for research purposes only. Not approved for human or veterinary use.

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