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Purity: | 99.0%min. | Molecular Formula: | C50H68N14O10 |
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Molecular Weight: | 1025.2 | CAS: | 32780-32-8 |
Peptide Content (N%): | >=80.0% | Acetate Content (HPIC): | <=15.0% |
MW: | 177.5 | ||
High Light: | hgh human growth hormone,human growth hormone somatropin |
PT-141 Acetate Bodybuilding Peptides Muscle Gain Treating Sexual Dysfunction
CAS No.: | 32780-32-8 | Other Names: | PT 141 | MF: | C7H15NO4 |
EINECS No.: | 258279-04-8 | Place of Origin: | ShangHai, China (Mainland) | Type: | Auxiliaries and Other Medicinal Chemicals |
Grade Standard: | Medicine Grade | Usage: | Animal Pharmaceuticals, Bodybuilding | ||
Model Number: | Purity: | 99%min | Product Name: | PT141 | |
Appearance: | Powder | Grade: | Medical | Standard: | USP Grade |
Colour: | White | Export Markets: | Global | Production Capacity: | 10000g |
Description
PT-141 (Bremelanotide) is a highly potent synthetic peptide analogue of α-MSH that may elicit aphrodisiac effects through stimulation of melanocortin receptors. PT-141 (Bremelanotide) consists of seven amino acids and is a cyclic, shortened lactam variant of alpha-Melanocyte-stimulating hormone (α-MSH), a multifunctional peptide that regulates a broad array of physiological functions. In studies, bremelanotide was shown to induce lordosis in an animal model and was also effective in treating sexual dysfunction in both men (erectile dysfunction or impotence) and women (sexual arousal disorder).
Specification
Name: PT-141
Synonyms: Bremelanotide, PT-141 Acetate
CAS #: 189691-06-3
Molecular Formula: C50H68N14O10
Molecular Mass: 1025.2 Da (g/mol)
Amino Acid Sequence: Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Purity
PT-141 has a peptide purity level that exceeds 99.0% as determined by HPLC and MS. This peptide was synthesized with no additives and is supplied as a white lyophilized (freeze-dried) powder.
Usage
Bremelanotide, similarly to its analogues α-MSH and melanotan II, acts as a non-selective agonist of all of the melanocortin receptors except MC2, where it lacks significant affinity. Reported activity of the drug is as follows:
MC1 (Ki = 0.68 nM)
MC2 (Ki > 1000 nM)
MC3 (Ki = 72.07 nM)
MC4 (Ki = 19.25 nM)
MC5 (Ki = 166.8 nM)
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