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Retatrutide

Price range: $55.00 through $300.00

Retatrutid is a novel peptide drug and triple receptor agonist acting on GLP-1, GIP, and glucagon receptors. It aids in weight reduction by regulating appetite, enhancing satiety, and increasing energy expenditure. Retatrutid also improves cardiovascular-metabolic risk markers such as blood pressure, HbA1c, fasting glucose, insulin, cholesterol, and triglycerides. Furthermore, it benefits non-alcoholic fatty liver disease patients by normalizing liver fat. Unlike single or dual agonists, Retatrutid’s triple action mechanism offers more extensive metabolic benefits, making it more effective for weight loss, liver fat reduction, and blood sugar normalization. Retatrutid is a promising new treatment option for obese and type 2 diabetic patients, especially those unresponsive to current treatments.

The peptide will be provided as lyophilized powder to ensure maximum stability.
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Description

▎Retatrutid  Overview

Retatrutid is a novel peptide drug. As a triple receptor agonist, it acts on the glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glucagon receptors simultaneously. It helps individuals lose weight by comprehensively regulating appetite, enhancing satiety, suppressing hunger, and increasing energy expenditure.

In addition, Retatrutid can also improve multiple cardiometabolic risk indicators, such as blood pressure, glycated hemoglobin, fasting blood glucose, insulin, total cholesterol, low-density lipoprotein cholesterol, and triglycerides. It also has a positive effect on patients with non-alcoholic fatty liver disease, enabling the liver fat content of most participants to return to normal.

Compared with single or dual agonists, Retatrutid regulates blood glucose, body weight, etc. from multiple dimensions by simultaneously activating the three receptors of GLP-1, GIP, and glucagon (GCG). Theoretically, it can more comprehensively improve metabolic disorders and has unique advantages in aspects such as weight loss, reduction of hepatic steatosis, and normalization of blood glucose levels.

The synergistic action of multiple receptors of Retatrutid makes it more effective than existing GLP-1 receptor agonists or dual receptor agonists in regulating metabolism and controlling body weight, providing new treatment options for patients with obesity and type 2 diabetes mellitus.

▎Retatrutid  Structure

Sequence: YA⊃1;QGTFTSDYSI-L⊃2;LDKK⁴AQA⊃1;AFIEYLLEGGPSSGAPPPS⊃3;

Molecular Formula: C221H342N46O68

Molecular Weight: 4731 g/mol

CAS Number: 2381089-83-2

PubChem CID: 171390338

Synonyms:LY3437943

Retatrutid  Research

What is the research background of Retatrutid?

Obesity has become one of the prominent public health challenges in contemporary society. It can give rise to numerous health problems such as type 2 diabetes mellitus, cardiovascular diseases, hypertension, dyslipidemia, and non-alcoholic fatty liver disease. With the continuous increase in the incidence of obesity, there is an increasingly urgent need for new therapies that can effectively manage body weight and improve health conditions [1]. Although lifestyle interventions, such as increased physical activity and dietary control, are the core measures for weight mnagement, it is extremely difficult for many adult obese patients to maintain long-term weight loss.

Retatrutid, as a novel triple receptor agonist, can act on the glucagon-like peptide-1 receptor (

GLP-1R), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon receptor (GCGR). This multi-receptor mechanism of action endows it with significant advantages in the field of weight loss. Compared with weight loss drugs that act on only a single receptor, Retatrutid can more comprehensively regulate the body’s metabolic processes[1]. Retatrutid achieves weight loss by regulating multiple hormone receptors, not only showing remarkable efficacy but also having relatively mild gastrointestinal side effects. In addition, as a triple receptor agonist, Retatrutid has a more powerful weight loss effect and a wider range of applicable populations compared with other new weight loss drugs.

What is Retatrutid?

Retatrutid is a novel long-acting glucagon-like peptide-1 (GLP-1) receptor agonist. It is modified and optimized based on the structure of natural GLP-1, and it can specifically bind to and activate the GLP-1 receptor, exerting physiological functions similar to those of natural GLP-1, such as promoting insulin secretion, inhibiting glucagon secretion, delaying gastric emptying, reducing appetite, etc. It has broad application prospects in the treatment of diabetes and weight management.

What is the mechanism of action of Retatrutid?

The mechanism of action of Retatrutid stems from its agonistic effects on multiple receptors. Firstly, its agonistic effect on the glucagon-like peptide-1 receptor (GLP-1R) can increase insulin secretion, inhibit glucagon secretion, lower blood glucose levels, and at the same time delay gastric emptying, increase satiety, and reduce food intake [2]. Secondly, its agonistic effect on the glucose-dependent insulinotropic polypeptide receptor (GIPR) can promote insulin secretion, enhance glucose utilization, and affect fat metabolism, inhibiting lipolysis and promoting fat synthesis[2]. Moreover, the agonistic effect of Retatrutid on the glucagon receptor (GCGR) usually promotes glycogenolysis and gluconeogenesis in the liver, increasing blood glucose levels. However, under the action of Retatrutid, this glucose-raising effect is offset by the effects of the other two receptors, while promoting lipolysis and reducing fat accumulation [2]. This multi-target mode of action may be more effective in treating obesity than single receptor agonists.

By simultaneously activating these three receptors, Retatrutid can exert a variety of metabolic regulatory effects and produce therapeutic effects on obesity and related diseases. In terms of regulating blood glucose levels, since the activation of GLP-1R and GIPR promotes insulin secretion and inhibits glucagon secretion, and the activation of GCGR is offset by the effects of the other two receptors, Retatrutid can effectively regulate blood glucose levels, which is of great significance for the treatment of type 2 diabetes mellitus [1, 2]. In terms of reducing fat accumulation, the activation of GCGR promotes lipolysis and reduces fat accumulation, while the activation of GLP-1R increases satiety and reduces food intake, further reducing fat synthesis [1]. In addition, Retatrutid also has an improving effect on non-alcoholic fatty liver disease. It can reduce the fat content in the liver and improve liver function.

Additional information
Specification

5mg/vial, 10 vial/kits

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10 mg/vial, 10 vial/kits

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15 mg/vial, 10 vial/kits

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20 mg/vial, 10 vial/kits

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30 mg/vial, 10 vial/kits

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40 mg/vial, 10 vial/kits

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50 mg/vial, 10 vial/kits

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60 mg/vial, 10 vial/kits

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