PEPTIDE INFORMATION Contact Kitt Burkley for Pricing 855-762-4878
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PEPTIDE INFORMATION Contact Kitt Burkley for pricing 855-762-4878 AOD 9604 AOD 9604 works by mimicking the way natural HGH regulates fat metabolism but without the adverse effects on blood sugar or growth that is seen with unmodified HGH. Studies have suggested that AOD 9604 has an ability to stimulate lipolysis and inhibit lipogenesis. In addition AOD 9604 possesses other regenerative properties associated with growth hormone. Trials have been undertaken to determine the possible application of AOD 9604 in osteoarthritis and hypercholesterolemia, as well as for bone and cartilage repair. Results of oral glucose tolerance testing have demonstrated that AOD 9604 has no negative effect on carbohydrate metabolism, and it does not affect serum IGF-1 levels. AOD 9604 has an excellent safety profile and is generally well tolerated. It has attained Human GRAS status in the US. AOD 9604 600mcg/ml Cream – 30g AOD 9604* 0.5mg Troche BPC-157 (Body Protection Compound) BPC-157 promotes muscle and tendon healing, increases angiogenesis and decreases inflammatory response. Produces more type 1 collagen and has excellent potential for diabetic wound healing. BPC- 157 is highly stable, resistant to both hydrolysis and enzyme digestion. It can be given orally as well as administered subcutaneously or intramuscularly – no carrier molecule is required. This peptide has significant anti-inflammatory modulating effects. BPC-157 promotes tissue healing through signaling pathways – it provides specific response to particular injury thru cell signaling. BPC- 157 can be used continuously as body protective, or for specific period to treat body injury. BCP-157 is in clinical trials for IBD. Cytoprotective – it counteracts NSAID lesions in the GI tract, can help get patients of PPIs. BPC-157 10mg/vial – lyophilized BPC-157 0.5mg capsules Bremelanotide (PT-141) Bremelanotide is a peptide melanocortin receptor agonist. While it has been studied for treatment of sexual dysfunction in both men (erectile dysfunction) and women (sexual arousal disorder) it has been shown to be most effective in premenopausal women with hypoactive sexual desire disorder (HSDD). Bremelanotide does not act upon the vascular system, but directly increases sexual desire via the nervous system. Bremelanotide activates melanocortin receptors, but the mechanism by which it improves sexual desire is not understood. Contraindicated for patients with uncontrolled high blood pressure or in those with known cardiovascular disease, and is not recommended for patients at high risk for cardiovascular disease. Bremelanotide (PT-141) 20mg/vial – lyophilized Bremelanotide* (PT-141) 15mg/ml Nasal Spray – 4mL Dihexa Dihexa is a nootropic small peptide that was developed by researchers at Washington State University. It has been found to potently improve certain cognitive function of neurodegenerative conditions and potential trauma-based brain disorders through increased synaptogenesis. Dihexa has been found to potentiate the cellular actions of HGF (Hepatocyte Growth Factor). It is this ability to activate HGF that is responsible for both the synaptogenic and procognitive activities. Dihexa is orally active and able to permeate the blood-brain barrier, making it effective in either oral or topical forms of administration. Dihexa 20mg/ml transdermal cream – 30g Dihexa 5mg capsules Epithalon Epithalon is a synthetically-derived tetrapeptide whose sequence of amino acids is Alanine-Glutamate- Asparagine-Glycine. Epitalon’s primary role is to increase the body’s production of telomerase, a natural enzyme that helps cells reproduce telomeres, the protective parts of DNA. The longer the telomere strands are, the better cell health and replication function they provide. As people age, the production of telomerase falls and telomeres become shorter, resulting in declining cell replication and health. Epithalon’s ability to increase the production of telomerase strengthens and lengthens telomeres, thus it may assist in decreasing the aging process and improving general health and quality of life. Epithalon 15mg/vial – lyophilized GHK-Cu GHK-Cu is a naturally occurring copper complex found in the human body. Copper peptides are small, naturally occurring protein fragments that have high affinity for copper ions, which are critical to normal body function. GHK-Cu has a variety of roles in the human body including wound healing and infection control, attracting immune cells, anti-oxidant and anti-inflammatory effects, stimulating collagen and promoting blood vessel growth. It has also been found that GHK-Cu stimulates hair growth, with efficacy comparable to that of 5% minoxidil. It is widely used in anti-aging skin care products for its ability to firm the appearance, increase thickness, reduce wrinkles and increase collagen in photo-aged skin. GHK-Cu exerts its action on a variety of pathways in the human body due to the peptide sequence and copper’s ability to promote various functions. GHK-Cu 10mg/ml – 5ml vial* GHK-Cu 5mg/ml Topical Foam - 30ml GHK-Cu 1%/BioPeptides Cream – 30g Ipamorelin Ipamorelin is a growth hormone releasing peptide (GHRP). It suppresses somatostatin and increases the stimulation and release of growth hormone (GH) from the anterior pituitary. Ipamorelin increases release of hypothalamic GHRH in part by helping to overcome the diminished secretory capacity of the release neurons, which diminishes due to oxidative damage as the body ages. Ipamorelin therapy may help increase vitality and mental clarity and improve many of the unwanted health issues associated with aging such as lean muscle loss, fat gain, skin laxity, cognitive decline, poor sleep patterns and reduced bone density. It has demonstrated good safety and tolerability in human clinical studies. Ipamorelin 9mg/vial – lyophilized Ipamorelin 15mg/vial – lyophilized Ipamorelin Combos Ipamorelin may be administered by itself or in combination with a growth hormone releasing hormone (GHRH) – either Sermorelin or Modified GRF 1-29 (CJC 1295 without DAC). GHRHs stimulate the pituitary to increase or amplify the strength of growth hormone pulses, while Ipamorelin stimulates the frequency of growth hormone pulses. The goal of combining these peptides is to create synergy that stimulates the patient’s body to increase both the strength and frequency of growth hormone pulses, thereby creating a more youthful, natural and effective cycle of growth hormone release. Ipamorelin+Modified GRF 1-29 (CJC 1295 without DAC) 9mg/5mg per vial – lyophilized Ipamorelin+Sermorelin 9mg/9mg per vial and 15mg/15mg per vial – lyophilized Kisspeptin Kisspeptin is produced in the hypothalamus and acts upon KISS1 and GPR54 receptors to stimulate the release of several other hormones. It initiates the release of gonadotropin-releasing hormone (GnRH), which then stimulates the pituitary gland to release lutenizing hormone (LH) and follicle stimulating hormone (FSH). These hormones have a direct role in the production of testosterone and estradiol. Inadequate function of Kisspeptin can contribute to both male and female infertility. Kisspeptin has been indicated in the treatment of primary hypogonadism, a condition that causes insufficient production of testosterone (which plays a key role in masculine growth and health) and the inability to produce healthy sperm. Kisspeptin-10 – 200mcg troches Melanotan II Melanotan II is an analog of the peptide hormone alpha-melanocyte stimulating hormone (a-MSH) which induces skin tanning. Like its predecessor, Melanotan I, Melanotan II plays a role in stimulating melanogenesis and thus providing a protective mechanism against UV rays since under its actions melanocytes are able to increase production and secretion of hormone melanin. Another characteristic of this compound is its ability to induce erections in men with erectile dysfunction. Melanotan II 10mg/vial – lyophilized MK-677 (Ibutamoren) Ibutamoren (also known as MK-677) is a long-acting, selective agonist of the ghrelin receptor and a growth hormone secretagogue. It mimics the growth hormone stimulating action of the hormone ghrelin. Ibutamoren has been shown to increase the secretion of several hormones including GH and IGF-1and produces sustained increased levels of these hormones without affecting cortisol levels. Ibutamoren is orally administered, which makes it unique from other secretagogues. It requires only a once daily dose at bedtime and remains active for approximately 24 hours in the body. MK-677 (Ibutamoren) 12.5mg MK-677 (Ibutamoren) 25mg Selank Selank is a nootropic, anxiolytic heptapeptide. Clinical studies have shown that Selank has an anxiolytic effect comparable to that of benzodiazepine drugs without the undesirable potential side effects such as amnesia, confusion, drowsiness, dependency and withdrawal. In addition to its anti-anxiety and antidepressant properties, Selank can also enhance memory and cognitive function. This peptide can potentially replace stimulants, tranquilizers, and antidepressants. Selank is also considered to be immunomodulatory, capable of changing and improving the immune system. It can help with hyperglycemia, weight gain, and alcohol and opioid dependence. Selank is generally safe and well tolerated. Various clinical trials reported no drug interactions, allergic reactions or any dependence or withdrawal symptoms. Selank* 7.5mg/mL nasal spray – 3mL Semax Semax is a peptide best known for its nootropic, neuroprotective, and neurogenic/neurorestorative properties. Semax increases brain-derived neurotrophic