All products on this site are for In-Vitro Research, Development use only. Products are Not for Human consumption of any kind. All products on this site are for In-Vitro Research, Development use only. Products are Not for Human consumption of any kind.
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B7-33 Peptide For Sale

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What is B7-33 Peptide?

B7-33 is a soluble research peptide taken from the larger, naturally occurring protein H2-relaxin. It is impacting the musculoskeletal system, cardiovascular system, and reproduction. B7-33 retains the anti-fibrotic properties of relaxin without enhancing cAMP production.

B7-33 is more stable and therefore is preferred. It is being investigated as an anti-fibrotic agent in preclinical animal models of liver disease, systemic sclerosis, idiopathic pulmonary fibrosis, and other fibrotic conditions. There are currently five trials of B7-33 in clinical trials for different liver conditions. B7-33 has shown promise in preclinical models of liver disease and the next challenge is to establish how it will perform in human trials.

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How Does B7-33 Work?

B7-33 will have to show efficacy in treating liver fibrosis. It has not been formally tested in this context and it is likely that the disease is being challenged in ways it is not challenged in other liver diseases. The majority of liver disease is due to alcohol and other drugs rather than viral hepatitis and therefore the liver biology is completely different. The fibrotic process in chronic alcoholics appears to differ from that seen in viral hepatitis.

B7-33 Mechanism of action

The mechanisms by which B7-33 reduces fibrosis in models of chronic alcoholism, which are not associated with viral hepatitis, are unknown but may be related to the anti-inflammatory action of B7-33 and reduction of the TGF-β signaling pathway. Furthermore, in alcoholic models of liver disease, B7-33 seems to attenuate liver regeneration ([@B34]), which may be important in preventing a second hepatectomy. Thus, B7-33 is likely to be efficacious in alcoholic liver disease and probably in idiopathic liver fibrosis but will be tested in other disease states.

B7-33 Benefits

B7-33 also attenuates inflammation and oxidative stress. It does not appear to promote hepatic insulin resistance and it is safe in humans. These latter properties make it a potentially attractive alternative to anti-inflammatory drugs such as corticosteroids. It is important to note that the preclinical safety profile of B7-33, which is well established, is likely to be reproduced in humans.

B7-33 Trials

Other therapies in preclinical development for liver fibrosis include galectin-3 which mediates fibrosis and is an interesting therapeutic target since it acts as a ligand for E-cadherin on liver cells. There is one clinical trial in clinical trial in liver fibrosis with a galectin-3 antagonist, RG7213 but it is not known if the compound will reach clinical efficacy. Other therapies targeting inflammation include methotrexate, tetracycline derivatives, and the non-nucleoside antibiotic, doxycycline.

There are no clinical trials with either of these compounds for the treatment of liver fibrosis but the tetracycline derivatives are being evaluated for non-alcoholic steatohepatitis (NASH) in a clinical trial. Another potentially interesting therapy is metformin which decreases the liver injury and fibrosis induced by bile duct ligation and CCl~4~ in mice. It is hoped that further development of this drug will yield a better tolerated and effective therapy.

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B7-33 Peptide for Research Conclusion

A substantial body of preclinical evidence demonstrates that liver fibrosis can be reversed and that the fibrosis is associated with a profibrogenic T-cell population. There are several drugs in development, targeting the fibrogenic T-cell and/or profibrogenic cytokine pathways, for this indication. None are yet in clinical use but some may be in the future. We await the outcome of the first clinical trial in NASH in a couple of years. If the drug has efficacy and safety profile in this condition then it may transform the management of NASH and liver fibrosis. In time, these findings may apply to other liver diseases. A recent report demonstrated that a small molecule that targets the T-cell receptor on T-cell subpopulations prevented fibrosis in several mouse models of fibrosis and the authors called for the development of new molecules that target similar cellular pathways.


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Aicar for Sale

AICAR FOR SALEAICAR for sale here today for research and development study. We only supply premium quality AICAR peptides for study use. You will not be disappointed our research peptides are at least 99% pure.

Can you Buy AICAR?

In recent years, AICAR has been in the news a number of times as a novel substance athletes have turned to for performance enhancement.

For example, the popular weight-loss supplement phentermine is actually a prodrug for AICAR. The drug phentermine is the prodrug of AICAR, meaning that it is changed into AICAR during the digestion process in the stomach. This means that AICAR is a much more potent performance-enhancing drug than phentermine itself and as a result has been marketed as a “fat burner” supplement.


What is AICAR Peptide?

Although not as well known, AICAR itself is a great performance-enhancing substance as well. The substance AICAR has been marketed as a nutritional supplement and in recent years has become a major player in sports supplements.

AICAR is a derivative of the compound cAMP. There are many different types of AICAR, all of which are variations of cAMP but all with very similar effects.

What are the benefits of AICAR?

AICAR has many benefits that make it a popular drug among athletes. For starters, it is relatively cheap. Unlike most other performance-enhancing supplements, AICAR is readily available, is low-cost and you can purchase it online in small or large quantities.

Second, AICAR is a great performance-enhancing drug that enhances fat burning and increases overall energy levels.

There is also research suggesting that AICAR may be useful in the treatment of other diseases such as chronic inflammation and type II diabetes.

What AICAR Dosage Can Do!

AICAR is also an important signaling compound, meaning that it’s important for cells to stay in the right place and to produce the right amount of energy. AICAR keeps the body in the right place and keeps the energy in the right place for the most optimal performance.

AICAR also provides an advantage in terms of exercise performance by improving carbohydrate metabolism and energy supply in the muscle cells.

AICAR has been reported to increase exercise endurance and improve energy levels by increasing the breakdown of glycogen in the muscles.

Also, a study conducted at the University of California – San Francisco, showed that AICAR, when injected with the right dose, can improve exercise endurance and energy levels.

What are the side effects?

There are also some downsides to AICAR that should be taken into account. AICAR has been reported to cause some adverse side effects and should not be used by people with certain health conditions.

For example, the substance AICAR is a strong activator of the immune system, meaning that some of the benefits of the substance AICAR could be reversed or offset by this. AICAR also causes an increase in the production of the hormone cortisol. Therefore, people with a history of high cortisol levels or those with Cushing’s disease are better off avoiding the substance.

If you have a history of high cortisol levels or Cushing’s disease then you should probably avoid AICAR, or another one of the AICAR-like substances such as the hormone irisin, because of this risk.

If you do not have any medical conditions or experience any side effects after long-term use of AICAR, then there are several potential benefits to using the substance. AICAR can help with weight loss, increase exercise endurance, and also boost the breakdown of fatty acids.

Can I use AICAR to increase strength?

Yes. Although AICAR is considered an energy booster and helps with fat loss, it also has some very useful properties in regard to strength training. It is an important cellular signaling agent and helps the muscles to recover more quickly from exercise.

As a result of the positive effects of AICAR on muscle, AICAR has been found to be useful in increasing the maximum strength gains after training.

This substance can also help with recovery. This substance actually improves the recovery of the muscles after a workout, meaning that AICAR could be effective for athletes who wish to enhance their recovery from workout to workout.

When working out, athletes can use AICAR before and after a workout. AICAR can be used before and after a workout to help with the recovery of the muscles after exercise.

How can AICAR increase weight loss?

There are several reasons why AICAR can help with weight loss. One of the main reasons is the compound AICAR acts as a powerful catalyst for fat loss. It can also break down fat from your body quickly and efficiently.

AICAR has also been found to reduce the body’s ability to store fat, meaning that AICAR will not help with weight loss if it comes from an increase in the amount of fat stored in your body.

There is also a way to improve fat burning by combining AICAR with a fat loss drug such as phentermine or orlistat.
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What if I want to try AICAR but I’m concerned about the side effects?

One of the main reasons that athletes use AICAR is to increase their metabolism. Athletes who want to enhance their metabolism and see the best results with fat loss or weight loss are usually those who are looking for quick fat burning.

Is Aicar illegal?

With this in mind, it is not surprising to find that AICAR is quickly becoming a popular substance that has been approved by the FDA for use in adults.

In fact, AICAR has actually been approved by the FDA for long-term use.

AICAR’s long-term use has been approved and as a result, many athletes around the world are turning to AICAR to see if it is effective for weight loss or fat loss.

There are, however, some downsides to long-term use. These downsides include the following:

• Side effects

• Unwanted side effects

The side effects that can be experienced when taking AICAR for long periods of time include the following:

• Coughing

• Skin rash

• Nausea

• Fatigue

• Headache

The symptoms mentioned above are mild and are not considered dangerous.

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If you are an athlete or someone who is planning to lose weight or who is using AICAR for other reasons, the substance can be used, however, you should be aware that it does not always give the best results.

A good tip to take into account if you are using AICAR is to take it with a lot of caution and do so under the supervision of a doctor. It is also a good idea to avoid this substance if you are using it as part of a strict diet or if you suffer from any medical conditions.

Are there any health issues that AICAR can cause?

AICAR is considered to be relatively safe, however, there are some downsides to using the substance. If you are planning to use this substance, make sure to be aware of the possible adverse side effects and medical issues that may be experienced.

The most common side effects are those that are experienced when using caffeine. In a dose, AICAR is unlikely to cause these problems. Caffeine is relatively harmless, however, if you are planning on using a stimulant such as AICAR, you should be aware of the dangers and side effects that can be caused.

An issue that you should be aware of when using AICAR is the possibility of low blood pressure. AICAR is known to cause this in some people, meaning that athletes or individuals who want to lose weight are better off to avoid the substance.

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If you have a medical condition such as a blood pressure problem or heart disease you should be aware that AICAR is not recommended.

AICAR can cause you to develop low blood pressure. Blood pressure is an important indicator of your health, so if you have a medical condition such as heart disease or high blood pressure you should probably avoid AICAR.

The other main reason that people avoid this substance is that it causes some unwanted side effects that can be dangerous if used in large amounts.

These unwanted side effects include some of the following:

• Chest pains

• High blood pressure

• Headache

• Fatigue

• Muscle cramps

• Nausea

If you are planning on taking the substance, make sure that you inform the doctor that you are planning to use AICAR if you suffer from any medical conditions.

A lot of people have used AICAR safely for many years but sometimes there can be unwanted side effects, some of which can be dangerous.


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Buy Hexarelin

Buy Hexarelin today for education and researchbuy hexarelin into new medical treatments. Hexarelin is available in 2mg and 5 mg vials for use in development and finding new pharmaceuticals. We want you to buy Hexarelin from a reputable source so for those in the research and science community. So choose us today to buy Hexarelin peptide!

What is Hexarelin used for?

Hexarelin is a potent, synthetic, peptidic, orally-active, centrally-penetrant, and highly selective agonist of the ghrelin/growth hormone secretagogue receptor (GHSR) and a growth hormone secretagogue. It stimulates the secretion of growth hormone (GH) and stimulates appetite in both humans and rodents. It’s anabolic and orexigenic effects have made it an interesting substance for treating metabolic diseases and anorexia nervosa. It is currently under clinical development in a number of conditions in which the loss of lean body mass is a problem. In this review, we discuss the pharmacology, pharmacokinetics, efficacy, and safety of Hexarelin in humans. We also discuss the possible mechanism of action of Hexarelin.

Is Hexarelin a GHRH?

Hexarelin, a peptidyl analog of growth hormone secretagogue-1a (GHS-1a), is a synthetic growth hormone secretagogue that stimulates the secretion of GH, an effect that is mediated via a specific binding site on the growth hormone secretagogue receptor (GHRH). Growth hormone secretagogue (GHS)-1a is a cyclic peptide (GH~3~–GHS–NH~2~) that binds and activates the same receptor as ghrelin, a 28-amino acid hormone secreted by the stomach that stimulates the secretion of growth hormone (GH) and appetite. GHS-1a is an endogenous peptide that was initially identified as a circulating factor in the rat that stimulated the secretion of growth hormone (GH) (Kojima et al., 2001).

Later, Kojima et al. (2004) characterized a partial GHS-1a gene from the human hypothalamus and characterized a human ghrelin receptor (GHSR) that was highly homologous to the rat ghrelin receptor.

In addition, they reported the presence of the same GHS-1a gene in human pancreatic islets, suggesting that this peptide may be synthesized in the pancreas and/or in the gastrointestinal tract. Subsequently, this molecule was described in fish (Zwahlen et al., 2004).

What is the Chemical structure of Hexarelin?

The ghrelin receptor belongs to a new class of G protein-coupled receptors, which are known to mediate the secretion of GH. This receptor is located primarily in the hypothalamus and pituitary and is expressed in the arcuate nucleus, medial hypothalamus, and ventromedial nucleus. The ghrelin/GHSR system is involved in the regulation of energy balance and it was first identified in rats (Kojima et al., 2001), later in mice (Pelleymounter et al., 2002), and more recently in humans (Schuelert et al., 2002). In a series of studies using a variety of receptor subtypes and cellular signaling pathways, it was confirmed that ghrelin has a potent orexigenic effect in the brain by acting on several sites, including the arcuate nucleus (ArcN) and the ventral tegmental area (VTA). It also stimulated the release of growth hormone (GH) and stimulates feeding behavior by activating neurons in the ArcN, which may be related to the regulation of the synthesis and release of other substances in the hypothalamus.

What peptides are like HGH?

Ghrelin and GHS-1a interact with the same receptor (ghrelin receptor), which is highly homologous to the binding site of the endogenous ligand, ghrelin. It is the only peptidyl receptor described so far that does not contain a cysteine residue, unlike most receptors. In addition, the ghrelin/GHSR interaction activates signaling pathways different from the typical receptor-ligand interaction. These data indicate that this receptor is a special member of the G protein-coupled receptor family, called a selective receptor. The binding of ligands to this receptor may affect the activation of multiple receptors such as P2X purinoceptors, opioid receptors, and the adenosine-1 receptor.

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In mice, the expression of the GHSR gene and its peptide ligand was found in the pituitary, ArcN, and VTA. GHS-1a, a synthetic peptidyl agonist of the GHSR, is a highly selective ligand with a 1000-fold greater potency than ghrelin in stimulating the secretion of growth hormone (GH) and inducing food intake in rats. In addition, GHS-1a is an efficient GH secretagogue in human adipose tissue, whereas ghrelin did not stimulate the secretion of GH in human adipose tissue (Tschöp et al., 2004). These data indicate that GHS-1a and ghrelin function by binding to the same receptor and activating distinct pathways. GHS-1a has a unique pharmacological profile that is unlike that of ghrelin. Both GHS-1a and ghrelin have the same primary amino acid sequence (GH~3~–GHS–NH~2~).

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However, there are some differences in the amino acid sequences of these peptides in the C-terminus region, making these two peptides not identical. The peptides differ only in the replacement of Tyr (Tyr-3), by Phe (Phe-3) in GHS-1a, in addition to a Glu/Asp exchange in the hexarelin sequence (Phe-3–Glu–Lys–Asp–Tyr-3–His-5) in the hexarelin peptide. The GH-releasing properties of GHS-1a and its analogs, which do not include the Phe-3 sequence, have been investigated (Blevins and Kelly, 1994; Zwahlen et al., 2004). These studies indicate that the Phe-3 sequence and a positive charge are important for ghrelin\’s activity. Therefore, the Glu/Asp exchange in hexarelin (Phe-3–Glu–Lys–Asp–Tyr-3–His-5) may have contributed to the anabolic effects of hexarelin. Furthermore, a study in hypophysectomized rats (Cadet et al., 2004) found that GHS-1a can act in concert with other hypothalamic neuropeptides to enhance the secretion of GH. Thus, the hypothalamic peptides that have an anabolic effect, such as growth hormone-releasing hormone (GHRH), stimulate the synthesis of GHS-1a, which in turn stimulates the secretion of GH. Therefore, GHS-1a may function as a neurotransmitter that serves as a link between peptides and other brain cell types.

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The GHSR is a member of the class B group of the rhodopsin-like family of G protein-coupled receptors, a class that includes the secretin receptor, β~2~ adrenergic receptor, and muscarinic acetylcholine receptors. This group of receptors is characterized by a seven-transmembrane domain structure, a relatively long extracellular loop and an intracellular loop. A number of important structural features of the GHSR allow its activation by ghrelin or GHS-1a (Kojima et al., 2004; Wurtman et al., 2004). These structural elements include the C-terminal sequence of the receptor, its relatively long extracellular loop, its intracellular loop, and the first two transmembrane domains. In addition, specific substitutions of amino acids are located in the loops.

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Gonadorelin For Sale

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Is Gonadorelin a peptide?

Gonadorelin is a research peptide that is the same as gonadotropin-releasing hormone (GnRH) that is naturally released from the hypothalamus gland. GnRH causes the pituitary gland to release other hormones (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]). LH and FSH control development in children and fertility in adults. Gonadorelin helps fertility and helps with menopausal symptoms. It is used for women who have low estrogen levels, have a history of multiple abortions, and have not responded to previous hormone treatments.

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How do you administer Gonadorelin?

For an oral tablet, an injectable, a topical ointment, or a topical vaginal ring, see FDA Product Information on Contraceptives and Hormone Replacement Therapy.

Tablets, Oral Solution, or Gel

Do not use it in pregnancy or during lactation. Female patients of childbearing potential should use effective contraception during treatment with this medicine and for at least 2 months after the last dose. Do not use it in children.

Gonadorelin Side Effects?

Drugs used in the treatment of endometriosis or polycystic ovary syndrome may cause serious adverse reactions when used with gonadorelin.


Adverse reactions have been reported. Serious adverse reactions may be life-threatening and can include: blood clots, stroke, cardiovascular problems, and a condition called tumor lysis syndrome. Consult your doctor for more information.



If a woman is planning to become pregnant or is pregnant, gonadorelin should be used only when clearly needed and strictly according to the instructions provided by your doctor. The safety of gonadorelin in pregnancy is not known. If used in a woman who is pregnant, gonadorelin may cause an abortion. Gonadorelin should be used with caution if there is a risk of miscarriage (loss of early pregnancy or spontaneous abortions). Gonadorelin is not indicated for the treatment of ovulation disorders or menstrual disorders. It is contraindicated for women with active, severe systemic lupus erythematosus, or when gonadorelin is used as a contraceptive.

Severe hypersensitivity to this drug has been reported. A severe allergic reaction, e.g., anaphylaxis, occurs in less than 1% of patients receiving gonadorelin. Closely monitor patients for symptoms of hypersensitivity during therapy with gonadorelin. Discontinue gonadorelin therapy if an allergic reaction occurs. Injections should be given using medical facilities equipped to deal with anaphylactic reactions.

Contraceptive Effects

Gonadorelin should be used to support fertility in a natural cycle only. Do not use it to prevent pregnancy (contraception). It should be used with caution in women of childbearing potential who do not wish to become pregnant. If you are a woman of childbearing potential (including adolescents), plan your pregnancy carefully. Do not assume that you will be pregnant because you are being treated with this drug. Consult your doctor if you are not certain of your pregnancy status (See PRECAUTIONS).

Do not use an injectable solution of gonadorelin for injection in women who are or plan to become pregnant. Gonadorelin is used only to support fertility. Do not use it to prevent pregnancy (contraception). It should be used with caution in women of childbearing potential who do not wish to become pregnant. If you are a woman of childbearing potential (including adolescents), plan your pregnancy carefully. Do not assume that you will be pregnant because you are being treated with this drug.

Ovulation Disorder

Use gonadorelin only to help women ovulate or to induce ovulation. Do not use to prevent pregnancy (contraception). Do not use this drug to support ovulation in women whose ovulation is not controlled by medications. If you are being treated for an ovulation disorder, you should follow your doctor’s instructions carefully. Do not increase the frequency of your menstrual periods.

Is there a High Risk of a Heart Attack?

Gonadorelin should be used only to help support fertility in women at high risk for a heart attack or who have a history of heart disease. Gonadorelin should be used with caution in women with a history of a previous myocardial infarction, angina, coronary bypass surgery, angioplasty, or stroke. Do not use gonadorelin in the following conditions:

  • Uncontrolled hypertension,
  • Myocarditis or cardiomyopathy (in patients with previous heart disease),
  • Sudden, unexplained, severe weakness,
  • Any disease that may lead to sudden cardiac arrest (e.g., ventricular tachycardia or cardiac arrest).

Gonadorelin For Sale and Important Safety Information


Do not use in combination with GnRH agonists, other gonadotropin-releasing hormones, GnRH analogs, or GnRH-receptor antagonists. The use of GnRH agonists and analogs, and GnRH antagonists may increase the risk of bone loss in women taking gonadorelin.

Caution is advised in patients with a history of diabetes, hypertension, cardiovascular disease, coronary disease, or in those with hyperlipidemia or a tendency to hyperlipidemia.

Use caution in patients with a history of heart disease or arrhythmias.

Take care when giving a dose of gonadorelin subcutaneously in women of childbearing potential.

Use caution in elderly patients, patients with a history of a recent heart attack or stroke.

Do not administer to women in labor, those with risk factors for the acute coronary syndrome, or patients with myocarditis, pericarditis, or unexplained prolonged QTc interval.

Take care with gonadorelin in patients with risk factors for cardiovascular disease (e.g., hypertension, hyperlipidemia), or a history of cardiovascular disease (e.g., coronary artery disease, myocardial infarction, angina, stroke, and transient ischemic attack).

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All products on this site are for In-Vitro Research, Development use only. Products are Not for Human consumption of any kind.