Medical Grade CAS 121062-08-6 Weight Loss Peptides 10mg/Vial Melanotan-II For Rrectile Dysfunction

Medical Grade CAS 121062-08-6 Weight Loss Peptides 10mg/Vial Melanotan-II For Rrectile Dysfunction

Melanotan-II (MT-II)

Melanotan-II (MT-II)/Cas No.: 121062-08-6
Product Name:Melanotan II
Synonyms:Acetate Melanotan II
Sequence: Ac-NLE-c[ASP-His-d-PHE-ARG-TRP-LYS]-NH2 Chemical Bridge Asp2-Lys7
Purity (HPLC): 98.0%
CAS:121062-08-6
Appearance: White powder
Molecular Formula: C50H69N15O9
Molecular Weight: 1024.18

Melanotan-II specification
Single Impurity (HPLC): 0.5%max
density :1.43
Amino Acid Composition: ±10% of theoretical
Peptide Content (N%): ≥80.0%
Water Content(Karl Fischer): ≤8.0%
Acetate Content(HPIC): ≤10.0%
Specific Rotation (20/D): -55.0～-65.0°(c=1 1%HAc)
MS(ESI): Consistent
Mass Balance: 95.0~105.0%
density:1.43

Melanotan-Ⅱ Introduction
Melanotan-Ⅱ is a new ring a- melanocyte stimulating hormone analogs, the product may be used to move from the treatment of psychological disorders. This product is a way to speculate on the effects on the CNS level before moving from. This double-blind study in 10 cases determined rational erectile dysfunction in men (18 to 60 years old) in the form of a cross in the abdominal wall subcutaneous injection for the 0.025 ~ 0.157mg / kg or saline placebo. Between the administration of the product and placebo over a 24-hour washout period. After each injection, patients monitored for 6 hours, and the patient is asked to avoid irritation. This product after injection eight cases men have erectile (mean duration of 144 minutes, and sufficient for sexual intercourse), and no one has this effect after the placebo injections. No pain when moving from erectile start time from 15 to 270 minutes (average 127.5 minutes). The researchers noted that the FDA in the home plus sexual stimulation may straining started sooner. Compared with placebo, the product significantly the most common adverse reactions are nausea, yawning, and decreased appetite. However, the present product g dose of 0.025mg people but no reports of serious adverse reactions.

Melanotan II COA:

A Potential Treatment For Skin Cancer:

It is known that the effects of α-MSH are mediated by melanocortin receptors.

MC1R is expressed in skin cells and has a high affinity for α-MSH and is the main receptor by which α-MSH signals.

Based on this fundamental information and observations of how α-MSH impacts melanomic cells, one study has hypothesized that "α-MSH acts initially to reduce initial tumor spread, but paradoxically protects those cells that escape from the primary tumor.

As an analog of α-MSH, it is logical to believe that Melanotan II may have similar effects.

Treatment For Male And Female Sexual Dysfunction:

Melanotan-1, the precusor to Melanotan II, would eventually be licensed for commercialization as a tanning agent and has been in development for use as a potential "therapeutic tan," with minimal need for prolonged sun exposure. In the initial clinical testing of Melanotan II, an immediate and unexpected response was noted. The main subject experienced an erection shortly after administration. It was suggested that Melanotan II "may prove equally effective in women" as a "treatment of female sexual dysfunction. At least one study has observed that administration of Melanotan II may increase sexual desire, which should warrant further "investigation of centrally acting agents on disorders of sexual desire.

Theoretically, Melanotan II may enhance sexual function in males (erectile activity) and females (increased levels of sexual desire and genital arousal). Unlike other sexual-enhancement drugs, it is hypothesizedd that Melanotan II works at a neurological level, eliciting a more "natural" sexual response with minimal side effects. It was suggested that Melanotan II "may prove equally effective in women" as a "treatment of female sexual dysfunction. [5] At least one study has observed that administration of Melanotan II may increase sexual desire, which should warrant further "investigation of centrally acting agents on disorders of sexual desire.

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