Bremelanotide Sexual Stimulation Growth Hormone,
PT-141 Sexual Stimulation Growth Hormone
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|Appearance:||White Powder||Specification:||10 Mg/vial|
|Shipping Method:||EMS, HKEMS, FEDEX, DHL, UPS, Aramex, ETC||Product Name:||PT-141|
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PT-141 (Bremelanotide) is the first of a new class of drugs called melanocortin agonists being developed to treat sexual dysfunction.The mechanism of action of PT-141 (Bremelanotide) may offer significant safety and efficacy benefits over currently available products because it acts on the pathway that controls sexual function without acting directly on the vascular system.Clinical data indicates that PT-141 (Bremelanotide) may be effective in treating a broad range of patients suffering from ED.The nasal formulation of PT-141 (Bremelanotide) being developed is as convenient as oral treatments, is more patient-friendly than invasive treatments for ED, such as injections and trans-urethral pellets, and appears to result in a rapid onset of action.
Bremelanotide, also known as PT-141, is a melanocortin peptide hormone. Bremelanotide (PT-141) was developed from Melanotan II (MT-2) and can be regarded as a derivate from MT-2. Bremelanotide (PT-141) is regarded as the only synthetic aphrodisiac. Studies have shown Bremelanotide to be effective in treating sexual dysfunction in both men (erectile dysfunction or impotence) and women (sexual arousal disorder).
Unlike and other related medications (PDE5s), PT-141 does not act upon the vascular system, but directly through the nervous system (hypothalamus) to increase desire. , Cials and are not considered aphrodisiacs as they do not have any direct effect on the libido. However, treatment with PDE5 inhibitors and PT-141 are known to have a synergistic effect.
PT-141 is a potential remedy for the treatment of sexual dysfunction; specifically, male erectile
dysfunction. Studies have shown that PT-141 does not act on the vascular system like former
compounds, but allegedly works by activating melanocortin receptors in the brain, therefore
helping increase ones sexual stimulation. PT-141 is a melanocortin based peptide that has
shown effectiveness in clinical studies on both male and female rats. Male rats have shown
erectile response with doses as low as 1-2 mgs whereas most female rats have shown positive
results with higher doses around 2-3 mgs. While the dosage requirements tend to be higher for
female rats, the observable results in female rats tend to be stronger.
PT-141 was developed from the Melanotan 2 Peptide, which underwent testing as a sunless
tanning agent. In initial testing, Melanotan 2 did induce tanning, but additionally caused sexual
arousal and spontaneous erections as unexpected side effects in nine out of the ten original male
volunteer test subjects. Palatin completed patient treatment in its Phase 2B clinical trial in
premenopausal women with FSD Primary data analysis and announcement of top-line results
anticipated in first-half of fourth quarter of calendar year 2012. In studies, PT-141 was shown to
be effective in treating sexual dysfunction in both men (erectile dysfunction or impotence) and
women (sexual arousal disorder). Unlike and other related medications, it does not act
upon the vascular system, but directly increases sexual desire via the nervous system.
|Melanotan I||10mg/vial ,10vial/box|
|Melanotan II||10mg/vial ,10vial/box|
|CJC 1295||2mg/vial ,10vial/box|
|CJC 1295 dac||2mg/vial ,10vial/box|
|PT 141||10mg/vial ,10vial/box|
|Frag 176 191||2mg/vial ,10vial/box|
|Frag176 191||5mg/vial ,10vial/box|
|PEG MGF||2mg/vial ,10vial/box|
|Thymosin Beta 4 (TB4)(TB-500)||2mg/vial ,10vial/box|
|Follistatin 344||1mg/vial ,10vial/box|
|Oxytocin 2mg||2mg/vial ,10vial/box|
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