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FTPP (Adipotide) is a peptidomimetic (a small protein-like chain designed to mimic a peptide), transformed into an experimental proapoptotic drug used for cellular death. Its purpose is to contribute in the weight loss. This substance has shown favorable results in tests and its main feature is its property of rapid loss weight.
Adipotide is designed to target specific blood vessels, supplying adipose tissue with blood. This process causes a shrinking effect on vessels, which forces the fat cells to feed on those vessels. All this mechanism gives origin to an apoptosis, which is a process of programmed cell death of multicellular organisms. There are two receptors where Adipotide binds: ANXA2 and prohibitin; these are found in blood vessels and accomplish the function of supplying white adipose tissue.
Palmitoyl Tetrapeptide-7 (PT-7) is a synthetic peptide comprised of four amino acids whose sequence is SSNA (Serine, Serine, Asparagine, Alanine). As in PP-4, palmitic acid is attached to the peptide chain as a penetration enhancer to drive the peptide through the stratum corneum. PT-7 was formulated with the goal of suppressing the body's production of excess interleukins, the chemical messengers which trigger the body's acute inflammatory response which leads to glycation damage.
Glycation is the process by which glucose links with proteins and causes them to bind together, thus stiffening tissues and leading to the complications of diabetes and some of the physiologic problems associated with aging. Glycation affects the skin's support system - collagen, elastin and other proteins - and leads to wrinkles, sagging, loss of youthful contours and uneven skin tone.
Inflammation is normally a protective response to tissue injury or destruction and is an important part of the body's immune response. It is the body's way of walling off a harmful agent and the injured tissue. Up to about age 35 when hormone levels begin to drop, very little interleukin is secreted and its secretion is strictly controlled.
However, as we age further, the hormonal regulatory system begins to break down and significant levels of interleukins are found in the plasma even when there is no inflammatory stimulus. This results in high levels of inflammatory proteins in the tissues, slow tissue regeneration, tissue rigidity and a loss of healing potential. This process has been linked with breast cancer, osteoporosis, anemia, autoimmunity and slower tissue regeneration.
Theoretically, if the production of excess interleukins can be suppressed, the inappropriate inflammatory response will not be triggered and glycation damage will be inhibited. This theory was borne out in the lab. In vitro, the Ultra Aesthetics scientists found that PT-7 induced a marked dose-dependent reduction in interleukin production. The higher the concentration of Palmitoyl Tetrapeptide-7, the greater the reduction in interleukin production - up to 40%.
UV radiation is known to accelerate interleukin production. When the scientists exposed cells to UV radiation and then added PT-7, they achieved an 86% reduction of interleukin production. These results show that PT-7 is able to affect baseline levels of interleukin as well as modulate the effects of UV-stimulated over-production.
Adipotide cycle and dosage
Adipotide is a new drug that is showing some promise in the area of obesity research. This drug was initially created as a cancer treatment designed to starve cancer cells of a blood supply so they would stop growing. The effects of Adipotide have shown that the drug actually starves fat cells of blood forcing them to die and be reabsorbed into the body. Initial tests were done on rats and then moved on to monkeys. The results from testing on rats showed a 30 percent decrease in body weight. After four weeks of daily injections of Adipotide followed by four weeks of non-treatment, 10 obese female rhesus monkeys lost an average of 11 percent of their body weight and 39 percent of fat deposits. Most of the loss was experienced during the non-treatment period.
High purity Polypeptides
|CJC-1295 DAC (Drug Affinity Complex)||2mg/Vial, 10Vials/kit|
|GHRP-2 (Pralmorelin)||10mg/Vial, 10Vials/kit|
|GHRP-2 (Pralmorelin)||5mg/Vial, 10Vials/kit|
|GHRP-6 (Growth hormone releasing peptide)||10mg/Vial, 10Vials/kit|
|GHRP-6 (Growth hormone releasing peptide)||5mg/Vial, 10Vials/kit|
|Melanotan-2 (MT2)||10mg/Vial, 10Vials/kit|
|Bremelanotide (PT-141)||5mg/Vial, 10Vials/kit|
|MGF(mast cell grow*th fac*tor)||2mg/Vial, 10Vials/kit|
|HG*H Frag 176-191||2mg/Vial, 10Vials/kit|
|HG*H 99.7% (Red, Yellow, Blue, Green Tops)||10IU/Vial, 10Vials/Kit|
|EPO Suspension||3000IU/Vial, 5Vials/Kit|
|EPO Powder||3000IU/Vial, 5Vials/Kit|
|IG*F1 Des1-3||1mg/Vial, 10Vials/Kit|
|IG*F1 LR3||0.1mg/Vial, 10Vials/Kit|
|IG*F1 LR3||1mg/Vial, 10Vials/Kit|
|Oxytocin Acetate; Oxtocin||2mg/Vial, 10Vials/kit|
|Thymosin β4 Acetate (TB500)||2mg/Vial, 10Vials/kit|
|Hexarelin Acetate||2mg/Vial, 10Vials/kit|
|Hexarelin Acetate||5mg/Vial, 10Vials/kit|
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