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Product info
Produktname: PT-141
Alias:Bremelanotid; BREMELANOTID; Brmelanotice; Ac-Nle-cyclo(-asp-his-d-phe-arg-trp-lys)-OH; Bremelanotid, PT141, PT-141; BREMELANOTID PT141; Brmelanotid; PT141
CAS: 32780-32-8
MF: C50H69N15O10
MW: 1040.17736
Aussehen: Freeze-dried powder
Water Content(Karl Fischer): ≤ 5.0%
Acetat-Gehalt(durch HPLC): ≤ 15.0%
Zusammensetzung der Aminosäuren: ± 10% of theoretical
Reinheit(durch HPLC): ≥ 97.0%
Einzelne Verunreinigung(durch HPLC): ≤ 1.0%
Peptid-Gehalt(von %N): ≥ 80%
Probe(Von Anhydrous, Frei von Essigsäure): 95.0~105.0%
Bacterial Endotoxins: ≤ 5EU/mg
MS(ESI):Consistent
Mass Balance:95.0~105.0%
PT-141 Usage
PT-141 in Men:
Effective in a broad range of patients, including those with severe ED and those non-responsive to sildenafil, effcacy in “at-home” studies is comparable to PDE-5 inhibitors up to 50% of ED patients were restored to a normal level of function coadministration with sildenafil shows superior efficacy side effects include facial flushing, Übelkeit, aftertaste and post-nasal drip
PT-141 in Women:
Palatin conducted a Phase 2A study in 18 premenopausal women with a diagnosis of female sexual dysfunction (FSD). Patients reported a significant increase in sexual desire and in genital arousal after receiving PT-141, compared to placebo. Additionally, there was a correlation between sexual desire and genital arousal in patients receiving PT-141, an observation that further reinforces the potential importance of these reports.
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.
