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Frag (176-191)

Description for Frag (176-191)

Frag (176-191) is a peptide derived from the growth hormone-releasing hormone (GHRH). Specifically, it is a fragment of the GHRH molecule, consisting of amino acids 176 to 191. This peptide is also known as AOD-9604.

Frag (176-191) is renowned for its potential fat-burning properties and its ability to promote weight loss. It works by targeting adipose (fat) tissues and stimulating the breakdown of stored fat, leading to increased fat metabolism. This selective action makes it a popular choice for those looking to reduce body fat and improve body composition.

One of the key advantages of Frag (176-191) is its specificity for fat cells. It has been shown to have minimal impact on glucose metabolism or insulin sensitivity, making it safer than other weight loss compounds. This means that it can help individuals shed fat without negatively affecting their blood sugar levels or causing insulin resistance.

Moreover, Frag (176-191) has been found to have potential anti-aging effects. It is believed to improve skin elasticity and reduce the appearance of wrinkles, making it appealing to those seeking to maintain a youthful appearance.

When it comes to dosing, Frag (176-191) is typically administered in the form of subcutaneous injections. The recommended dosage is around 2 milligrams (mg) per day, divided into multiple injections. It is important to note that dosage requirements may vary depending on individual factors such as weight, body composition goals, and overall health.

As with any peptide or medication, it is crucial to consult with a healthcare professional before starting Frag (176-191) or any other weight loss regimen. They can provide personalized advice, monitor your progress, and ensure it is safe and appropriate for your specific needs.

Please keep in mind that Frag (176-191) is a research chemical and is not approved by regulatory bodies for human use. Its use should be approached with caution, and any decision to use it should be made after careful consideration and consultation with a healthcare professional.

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    Boldenone Undecylenate, also known by its trade name Equipoise, is a synthetic anabolic androgenic steroid (AAS) that has gained popularity among athletes and bodybuilders for its various benefits. It was originally developed for veterinary use, specifically for the treatment of horses, but it has since found its way into the world of human performance enhancement.

    Boldenone Undecylenate belongs to the family of testosterone-derived AAS, and its chemical structure is derived from testosterone by adding a double bond between carbon atoms 1 and 2 of the steroid backbone. This modification enhances its anabolic properties while reducing its androgenic effects, making it a favorable choice for many users.

    One of the primary reasons why Boldenone Undecylenate is highly regarded is its ability to promote lean muscle mass growth. It stimulates protein synthesis within the muscle cells, leading to an increase in muscle size and strength. This effect is accompanied by a significant improvement in nitrogen retention, which further aids in muscle growth. Users often report experiencing lean muscle gains that are more sustainable compared to other steroids.

    Another noteworthy characteristic of Boldenone Undecylenate is its relatively slow but steady release into the bloodstream. This is due to the undecylenate ester attached to the parent compound, which allows for a prolonged action. As a result, users typically require fewer injections, making it a convenient choice for those who prefer less frequent dosing.

    One of the unique qualities of Boldenone Undecylenate is its ability to increase red blood cell production, a process known as erythropoiesis. This results in improved oxygen-carrying capacity and enhanced endurance. Athletes who engage in endurance-based sports often appreciate this effect as it allows for longer and more intense training sessions without experiencing fatigue.

    In addition to its anabolic and erythropoietic properties, Boldenone Undecylenate also exhibits a mild androgenic activity. This means that it can promote masculine characteristics such as increased facial and body hair growth, deepening of the voice, and improved libido. However, the androgenic effects are generally milder compared to other AAS, making it a popular choice for female athletes and bodybuilders.

    When it comes to dosing, the recommended range for Boldenone Undecylenate is typically between 200 to 600 mg per week. However, some experienced users may opt for higher doses, although this increases the risk of potential side effects. The compound has a long half-life, estimated to be around 14 days, which contributes to its sustained action in the body.

    As with any AAS, the use of Boldenone Undecylenate carries the risk of side effects. These can include acne, oily skin, increased aggression, mood swings, and potential suppression of natural testosterone production. It is important to note that individual response to the compound may vary, and some users may be more susceptible to certain side effects than others.

    To mitigate the potential side effects and optimize the benefits of Boldenone Undecylenate, it is crucial to follow appropriate cycling protocols and engage in post-cycle therapy (PCT). This involves the use of medications and strategies to restore natural testosterone production and minimize the risk of hormonal imbalances.

    In conclusion, Boldenone Undecylenate is a versatile and popular synthetic AAS that offers numerous benefits to athletes and bodybuilders. Its ability to promote lean muscle mass growth, enhance endurance, and exhibit mild androgenic properties make it an attractive choice for many users. However, it is important to approach its use with caution, adhere to recommended dosing guidelines, and prioritize post-cycle therapy to ensure optimal results and minimize potential side effects.



    Frag (176-191) is a peptide derived from the growth hormone-releasing hormone (GHRH). Specifically, it is a fragment of the GHRH molecule, consisting of amino acids 176 to 191. This peptide is also known as AOD-9604.

    Frag (176-191) is renowned for its potential fat-burning properties and its ability to promote weight loss. It works by targeting adipose (fat) tissues and stimulating the breakdown of stored fat, leading to increased fat metabolism. This selective action makes it a popular choice for those looking to reduce body fat and improve body composition.

    One of the key advantages of Frag (176-191) is its specificity for fat cells. It has been shown to have minimal impact on glucose metabolism or insulin sensitivity, making it safer than other weight loss compounds. This means that it can help individuals shed fat without negatively affecting their blood sugar levels or causing insulin resistance.

    Moreover, Frag (176-191) has been found to have potential anti-aging effects. It is believed to improve skin elasticity and reduce the appearance of wrinkles, making it appealing to those seeking to maintain a youthful appearance.

    When it comes to dosing, Frag (176-191) is typically administered in the form of subcutaneous injections. The recommended dosage is around 2 milligrams (mg) per day, divided into multiple injections. It is important to note that dosage requirements may vary depending on individual factors such as weight, body composition goals, and overall health.

    As with any peptide or medication, it is crucial to consult with a healthcare professional before starting Frag (176-191) or any other weight loss regimen. They can provide personalized advice, monitor your progress, and ensure it is safe and appropriate for your specific needs.

    Please keep in mind that Frag (176-191) is a research chemical and is not approved by regulatory bodies for human use. Its use should be approached with caution, and any decision to use it should be made after careful consideration and consultation with a healthcare professional.



    Methenolone acetate, commonly known as Primobolan, is a synthetic anabolic androgenic steroid (AAS) that has gained popularity among athletes and bodybuilders for its unique properties. With its origins dating back to the 1960s, Methenolone acetate has become a sought-after compound for individuals looking to enhance their performance and achieve a lean and sculpted physique. In this detailed description, we will explore the various aspects of Methenolone acetate, including its chemical structure, mode of action, benefits, side effects, and its place in the world of sports and fitness.

    Chemically, Methenolone acetate is derived from dihydrotestosterone (DHT) and features an added 1-methyl group, which alters its properties and makes it more resistant to metabolism in the liver. This modification allows Methenolone acetate to be orally active, making it a convenient choice for those who prefer not to use injectable steroids. The molecular formula of Methenolone acetate is C22H32O3, and it has a molecular weight of 344.50 g/mol.

    Methenolone acetate exerts its effects by binding to androgen receptors in various tissues throughout the body. This interaction activates specific signaling pathways, leading to an increase in protein synthesis, nitrogen retention, and an overall improvement in muscle growth and recovery. Additionally, Methenolone acetate exhibits low androgenic activity, making it a popular choice for female athletes seeking performance enhancement without the risk of virilization.

    One of the primary benefits of Methenolone acetate is its ability to promote lean muscle mass gains without excessive water retention or bloating. This characteristic makes it a preferred choice for individuals looking for quality muscle gains, especially during cutting phases or when aiming for a more defined and aesthetic physique. Methenolone acetate is often used in combination with other compounds to enhance its effects and create synergistic results.

    Another advantage of Methenolone acetate is its relatively mild nature concerning side effects. Compared to other steroids, it exhibits a low risk of aromatization, meaning it does not convert into estrogen. This quality eliminates concerns related to estrogenic side effects such as gynecomastia or excessive water retention. However, it is crucial to note that Methenolone acetate can still suppress natural testosterone production, leading to potential hormonal imbalances. To mitigate this effect, individuals often incorporate post-cycle therapy (PCT) protocols to restore natural testosterone levels.

    In terms of dosage and administration, Methenolone acetate is typically taken orally, in the form of tablets or capsules. The recommended dosage for men ranges from 50mg to 100mg per day, with some experienced users opting for higher doses. For women, the suggested dosage is significantly lower, usually ranging from 10mg to 25mg per day to minimize the risk of virilization. The duration of Methenolone acetate cycles varies depending on individual goals, but typical cycles last between 6 to 12 weeks.

    While Methenolone acetate offers several benefits, it is essential to be aware of potential side effects. Like any AAS, Methenolone acetate can negatively impact lipid profiles, leading to a decrease in HDL (good) cholesterol and an increase in LDL (bad) cholesterol. It is crucial to monitor cholesterol levels regularly and adopt a heart-healthy lifestyle, including a balanced diet and regular exercise. Other potential side effects of Methenolone acetate include acne, hair loss (in individuals predisposed to male pattern baldness), and virilization symptoms in women.

    In the world of sports and athletics, Methenolone acetate has been subject to controversy and bans due to its performance-enhancing properties. The World Anti-Doping Agency (WADA) and various sports organizations prohibit the use of Methenolone acetate and classify it as a banned substance. Athletes found to be using Methenolone acetate may face severe consequences, including disqualification, loss of medals, and even bans from future competitions.

    In summary, Methenolone acetate, or Primobolan, is a synthetic anabolic androgenic steroid that offers unique benefits for individuals seeking performance enhancement and muscle growth. Its ability to promote lean muscle gains, minimal estrogenic side effects, and relatively mild nature make it a popular choice among athletes and bodybuilders. However, it is essential to approach Methenolone acetate with caution, adhering to proper dosage guidelines and understanding the potential risks and side effects associated with its use.



    Tamoxifen is a medication that belongs to a class of drugs known as selective estrogen receptor modulators (SERMs). It is primarily used in the treatment and prevention of breast cancer, particularly in women with estrogen receptor-positive breast tumors. This medication has been widely studied and proven to be effective in reducing the risk of breast cancer recurrence and improving overall survival rates.

    Tamoxifen works by blocking the effects of estrogen in breast tissue. It does this by binding to estrogen receptors, preventing estrogen from attaching and stimulating tumor growth. By blocking estrogen, tamoxifen helps to slow down or halt the growth of cancer cells, reducing the risk of cancer spreading to other parts of the body.

    In addition to its role in breast cancer treatment, tamoxifen also has several other medical uses. It is often prescribed for women at high risk of developing breast cancer to help prevent the disease from occurring. Tamoxifen has been shown to significantly decrease the risk of developing both invasive and non-invasive breast cancer in these cases.

    Furthermore, tamoxifen has shown efficacy in treating certain types of breast cancer that have spread to other parts of the body, helping to control the disease and improve quality of life. It may also be used in combination with other medications or therapies to enhance its effectiveness.

    The dosage of tamoxifen can vary depending on the specific condition being treated, and it is usually taken orally in the form of a tablet. The treatment duration can range from a few years to several years, depending on the individual's response and risk factors.

    Like any medication, tamoxifen may have potential side effects. Common side effects include hot flashes, night sweats, fatigue, mood swings, and vaginal dryness. Some women may also experience more severe side effects such as blood clots, stroke, or endometrial cancer, although these are relatively rare.

    It is important to note that tamoxifen may interact with certain medications, so it is essential to inform your healthcare provider about any other drugs you are taking. Regular check-ups and monitoring are typically recommended while on tamoxifen to ensure its efficacy and safety.

    In conclusion, tamoxifen is a valuable medication in the treatment and prevention of breast cancer. Its ability to block estrogen receptors has been proven effective in reducing the risk of recurrence and improving survival rates. While it has potential side effects, the benefits of tamoxifen outweigh the risks for many individuals. Consultation with a healthcare professional is crucial to determine the appropriateness and dosage of tamoxifen for each individual case.



    Pfizer Genotropin 36IU is a synthetic human growth hormone (HGH) produced by Pfizer, a leading pharmaceutical company. It is designed to mimic the natural growth hormone produced by the pituitary gland in the body. Genotropin is widely used for various medical conditions related to growth hormone deficiency and has gained popularity in the field of sports performance enhancement.

    Key Features and Benefits:

    1. Growth Hormone Therapy: Pfizer Genotropin 36IU is primarily used for growth hormone replacement therapy in individuals with growth hormone deficiency. It helps stimulate linear growth and promotes the development of lean muscle mass.

    2. Improved Bone Density: Genotropin aids in enhancing bone mineral density, making it beneficial for individuals suffering from osteoporosis or other conditions that affect bone health.

    3. Enhanced Athletic Performance: Pfizer Genotropin has gained attention in the sports community due to its potential to enhance athletic performance. It is believed to improve muscle strength, endurance, and recovery, making it appealing to athletes and bodybuilders.

    4. Metabolic Benefits: Genotropin has metabolic effects such as increased protein synthesis, enhanced fat metabolism, and improved glucose utilization. This can lead to improved body composition, reduced fat mass, and increased muscle mass.

    5. Quality Manufacturing: Pfizer, a renowned pharmaceutical company, produces Genotropin under strict quality control measures. This ensures the product's reliability, safety, and efficacy.

    6. Convenient Administration: Genotropin is available in a pre-filled pen device, making it easy to administer the correct dose. The pen also allows for precise dosing adjustments, providing convenience and accuracy for patients.

    Usage and Dosage:

    The exact dosage and duration of treatment with Pfizer Genotropin 36IU should be determined by a qualified healthcare professional based on the individual's specific condition and growth hormone deficiency severity. Genotropin is typically injected subcutaneously (under the skin) using the provided pen device.

    Precautions and Side Effects:

    While Pfizer Genotropin is generally well-tolerated, there are potential side effects to be aware of, including:

    • Injection site reactions such as redness, swelling, or pain
    • Joint and muscle pain
    • Headaches
    • Fluid retention
    • Hypothyroidism (rare)

    It is important to discuss any existing medical conditions, allergies, or medications with your doctor before starting Genotropin therapy.

    Conclusion:

    Pfizer Genotropin 36IU is a synthetic human growth hormone manufactured by Pfizer. It is primarily used for growth hormone replacement therapy in individuals with growth hormone deficiency. With its potential benefits for bone density, muscle growth, metabolism, and athletic performance, Genotropin has gained recognition in both medical and sports communities. However, it is essential to consult a healthcare professional before starting any treatment with Genotropin to ensure its appropriate and safe usage.



    Clomid, also known by its generic name clomiphene citrate, is a medication commonly used in the field of reproductive medicine. It is primarily prescribed to women who are experiencing fertility issues due to ovulation problems. Clomid works by stimulating the release of hormones necessary for ovulation to occur.

    Clomid is available in tablet form and is typically taken orally once a day for a specific duration, as determined by a healthcare professional. The tablets come in different strengths, ranging from 25 mg to 100 mg. The dosage prescribed varies depending on the individual's medical condition and the response to treatment.

    When taken, Clomid acts on the pituitary gland in the brain, which then releases follicle-stimulating hormone (FSH) and luteinizing hormone (LH). These hormones are crucial for the development and release of eggs from the ovaries. By increasing the production of FSH and LH, Clomid helps to stimulate ovulation and increase the chances of conception.

    Before starting Clomid, it is essential to undergo a thorough medical evaluation to determine the underlying cause of infertility. This may involve assessing hormone levels, conducting imaging tests, and evaluating the overall reproductive health of both partners.

    It's important to note that Clomid is not suitable for everyone, and its use should be carefully monitored by a healthcare professional. Some individuals may have certain medical conditions or factors that make them unsuitable candidates for Clomid treatment. Additionally, Clomid should not be used if there is a known or suspected pregnancy, as it may cause harm to the developing fetus.

    Like any medication, Clomid may have side effects. Common side effects include hot flashes, mood swings, breast tenderness, nausea, and headaches. These side effects are usually temporary and resolve on their own. However, if any side effects persist or become bothersome, it is important to consult a healthcare provider.

    While Clomid is generally well-tolerated, there are some risks associated with its use. These include the potential for ovarian hyperstimulation syndrome (OHSS), multiple pregnancies (such as twins or triplets), and an increased risk of ovarian tumors. Close monitoring by a healthcare professional is essential to minimize these risks and ensure the safe use of Clomid.

    In summary, Clomid tablets are a widely used medication for women experiencing ovulation problems and infertility. By stimulating the release of hormones necessary for ovulation, Clomid increases the chances of successful conception. However, it is important to consult with a healthcare professional before starting Clomid and to closely follow their instructions throughout the treatment process.



    MT-II peptide, also known as Melanotan II, is a synthetic analog of the naturally occurring hormone alpha-melanocyte stimulating hormone (α-MSH). It is a peptide that has gained popularity for its potential use in melanogenesis, tanning, and sexual dysfunction treatment.

    Melanotan II was initially developed as a potential treatment for skin conditions such as erythropoietic protoporphyria, a genetic disorder that causes severe sun sensitivity. However, it was found to have additional effects on the body, particularly in relation to pigmentation and sexual function.

    One of the primary effects of MT-II peptide is its ability to stimulate melanocytes, the cells responsible for producing the pigment melanin. Melanin is responsible for the color of our skin, hair, and eyes. By binding to melanocortin receptors in the skin, Melanotan II increases the production of melanin, leading to skin darkening and tanning. This has made it popular among individuals looking to achieve a tan without excessive sun exposure.

    In addition to its pigmentation effects, MT-II peptide has also been studied for its potential use in treating sexual dysfunction. It has been shown to enhance sexual arousal and desire in both men and women. This effect is thought to be mediated through the activation of melanocortin receptors in the brain, which play a role in regulating sexual behavior.

    It is important to note that the use of MT-II peptide has some potential side effects. These can include nausea, flushing, increased blood pressure, and darkening of moles or freckles. Long-term use of Melanotan II is still being studied, and its safety and efficacy for various uses are not yet fully understood.

    It is crucial to consult a healthcare professional before using MT-II peptide or any other peptide-based product. They can provide guidance on its appropriate use, potential risks, and any contraindications based on an individual's medical history.

    Overall, MT-II peptide, or Melanotan II, is a synthetic peptide that has gained attention for its potential to induce skin darkening and enhance sexual function. While it may offer benefits for certain individuals, it is essential to approach its use with caution and under medical supervision.



    Oxymetholone, also known as Anadrol or A50, is a powerful oral anabolic steroid that has gained significant popularity among athletes and bodybuilders. This compound, derived from dihydrotestosterone (DHT), was first introduced in the 1960s by the pharmaceutical company Syntex under the brand name Anadrol.

    Oxymetholone is primarily used for the treatment of anemia, a condition characterized by low red blood cell count. It stimulates erythropoiesis, the production of red blood cells, by increasing the levels of erythropoietin, a hormone responsible for their formation. This property makes Oxymetholone a valuable tool in the medical field for patients suffering from anemia caused by various conditions such as chemotherapy, renal failure, or bone marrow disorders.

    In terms of its anabolic properties, Oxymetholone is considered to be one of the most potent steroids available. It has an incredibly high anabolic rating, surpassing that of testosterone. This means that it has a strong ability to promote muscle growth, increase strength, and improve athletic performance. Bodybuilders often incorporate Oxymetholone into their bulking cycles to maximize muscle mass gains.

    One of the primary mechanisms by which Oxymetholone enhances muscle growth is through its ability to increase protein synthesis. This process is crucial for muscle repair and growth, as it involves the production of new proteins within the muscle cells. By elevating protein synthesis, Oxymetholone creates an environment conducive to muscle hypertrophy, leading to larger and stronger muscles.

    In addition to promoting protein synthesis, Oxymetholone also enhances nitrogen retention in the muscles. Nitrogen is an essential component of amino acids, the building blocks of proteins. By maintaining positive nitrogen balance, Oxymetholone ensures that the body remains in an anabolic state, where muscle breakdown is minimized, and muscle growth is maximized.

    Another notable effect of Oxymetholone is its ability to increase red blood cell count. This leads to improved oxygenation and enhanced endurance. With more oxygen being delivered to the muscles, athletes can perform more prolonged and intense workouts, ultimately leading to improved performance and stamina.

    However, it is important to note that Oxymetholone also carries several potential side effects, which should be carefully considered before use. Due to its strong androgenic properties, it can cause androgenic side effects such as acne, oily skin, and increased body and facial hair growth. It can also lead to estrogenic side effects, including water retention, gynecomastia (development of breast tissue in males), and high blood pressure.

    Liver toxicity is another concern associated with Oxymetholone use. Being an oral steroid, it passes through the liver, where it can cause strain and damage. Therefore, it is recommended to limit the duration of Oxymetholone cycles and use liver support supplements to minimize the potential harm.

    As with any steroid, it is crucial to use Oxymetholone responsibly and under the supervision of a healthcare professional. It is generally recommended to start with a low dosage and gradually increase it to assess individual tolerance and minimize the risk of adverse effects.

    In conclusion, Oxymetholone is a powerful anabolic steroid that offers significant benefits in terms of muscle growth, strength enhancement, and increased red blood cell production. It is widely used in the medical field for the treatment of anemia and has gained popularity among bodybuilders and athletes seeking to maximize their performance. However, it is essential to be aware of the potential side effects and use Oxymetholone responsibly to ensure both short-term gains and long-term health.



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