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|Customized:||Customized||Packing:||Disguised Package Or As Required|
|Suitable For:||Adult||MOQ:||One Box|
Routes of administration :Intravenous, subcutaneous
Elimination half-life :2 hours
CAS No. :170851-70-4
Molar mass :711.85296 g/mol
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Delivery: Safe & timely, around 4-7days after payment
What is Ipamorelin
iPamorelin is one of the cleanest, most versatile and safest GHRP’s out there. The pentapeptide Ipamorelin is somewhat like Hexarelin, but it's cleaner. In some ways, it acts like GHRP-6 or GHRP – 2 without the sloppy sides of elevated hunger issues.
It should be emphasized that Ipamorelin is not only the most efficient, but also the safest and selective GH stimulant, since even at over-dosage Ipamorelin will solely stimulate growth hormone, without having an effect on the blood levels of prolactin and cortisol. This feature makes Ipamorelin attractive for professional sportsmen and it is currently arguably considered the best option from among all peptides stimulating the GH production (GHR peptides).
|Other Name||IpoMarelin; IpaMorelin Acetate; Aib-His-D-2-Nal-D-Phe-Lys-NH2; NNC 26-0161|
|Package||2mg/5mg per vial|
Ipamorelin (INN) (developmental code name NNC 26-0161) is a peptide selective agonist of the ghrelin/growth hormone secretagogue receptor (GHS) and a growth hormone secretagogue. It is a pentapeptide with the amino acid sequence Aib-His-D-2-Nal-D-Phe-Lys-NH2 that was derived from GHRP-1.
It significantly increases plasma growth hormone (GH) levels in both animals and humans. In addition,this drug stimulates body weight gain in animals. Like pralmorelin and GHRP-6, this drug does not affect prolactin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), or thyroid-stimulating hormone (TSH) levels.However, unlike pralmorelin (GHRP-2) and GHRP-6, but similarly to growth hormone-releasing hormone (GHRH), this product does not stimulate the secretion of adrenocorticotropic hormone (ACTH) or cortisol, and is highly selective for inducing the secretion only of GH.
The drug was originally developed by Novo Nordisk, and was investigated in phase II clinical trials by Helsinn Therapeutics for the treatment of postoperative ileus, but was discontinued due to lack of efficacy.
The drug has been used by athletes as a performance enhancing drug.
There are no spikes in cortisol or prolactin at lower doses.
Reduce body fat.
Anti-aging properties (faster recovery).
Improve sleep and mood.
How does it Work?
After the athlete being given the drug, a selective pulse is sent to stimulate the hypothalamic/pituitary to release GH. This pulse can last for about 3 hours after injection. Once the GH pulse is sent, the cells go straight into the muscles to support development while avoiding any possible bone or cartilage growth. This is good for users of this drug because long-term use can affect the growth of lean muscle without any possibility of bone or cartilage deformity. The same is true for synthetic HGH users, who have significant side effects in swollen joints and, in some cases, Carpel Tunnel. This product will increase cell synthesis, increase insulin secretion levels in pancreatic tissue, and increase ghrelin in the stomach - which helps release GH and control hunger. All of these features help promote fat loss, nutrient shuttles and build clean muscle mass.
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