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  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)

PT-141 (Bremelanotide) (10mg)

PT-141, also known as Bremelanotide, was derived from a synthetic Melanocortin known as Melanotan 2 (MT-2)
$40.00
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
  • PT-141 (Bremelanotide) (10mg)
SPECIFICATION

PT-141 (Bremelanotide) Peptide

PT-141, also known as Bremelanotide, was derived from a synthetic Melanocortin known as Melanotan 2 (MT-2). PT-141 is a Melanocortin that was developed to interact with Melanocortin-4 Receptor (MC-4R) and MC-1R. PT-141 has been studied for a variety of potential characteristics and bioactiviies, including implications in sexual dysfunction and cancer, and aiding hemorrhages.

Specifications

OTHER KNOWN TITLES: Bremelanotide

MOLECULAR FORMULA: C50H68N14O10

MOLECULAR WEIGHT: 1025.2 g/mol

SEQUENCE: Ac-Nle-Asp(1)-His-D-Phe-Arg-Trp-Lys(1)-OH

PT-141 Research

PT-141 PEPTIDE (BREMELANOTIDE) AND AROUSAL
PT-141 appears to uniquely stimulate the MC-4R, which may trigger cascades in the central nervous system which impact the brain region that controls sexual behavior.[1] The researchers suggest that “The erectogenic potential of PT-141, its tolerability profile and its ability to cause significant erections in [cases that otherwise] do not have an adequate response to a PDE5 inhibitor suggest that PT-141 may provide an alternative [avenue for ED research].” Studies in mice agonist binding to MC-4R reported sexual arousal and increased copulation activity in both males and females.[2] The mechanism of PT-141 appears to be different from compounds that manage blood flow to the genitals.[3][4] Researchers suggest that PT-141, potentially combined with existing modalities, may encourage both physiological and psychological alterations.

PT-141 PEPTIDE (BREMELANOTIDE) AND INFECTION
The MC-1R appears to mediate important anti-fungal and anti-inflammatory effects, as seen in one study using a rat model of specific fungal infection.[5] This may be relevant to PT-141 peptides as current compounds have limited mechanisms of action and may exhibit adverse effects in some cases. The alternative in PT-141 might impact morbidity and mortality, especially in immunocompromised cases.

PT-141 PEPTIDE (BREMELANOTIDE) AND HEMORRHAGE
In 2009, modified PT-141 was investigated for use in hemorrhagic shock. The peptide appears to control ischemia and protect tissues against inadequate blood supply hypovolemic (hemorrhagic) shock through interaction with both MC-1R and MC-4R. The modified version is referred to as PL-6983.

PT-141 PEPTIDE (BREMELANOTIDE) AND CANCER CELLS
The MC-1R receptor may be an important stimulus of DNA repair pathways, and is of relevance in cancer cell research.[6] The scientists reported that “MC1R signalling activates antioxidant, DNA repair and survival pathways.” Research models of variant MC-1R receptors appeared to be more prone to both basal cell and squamous cell carcinoma.[7] Altered PT-141 was suggested to be efficacious in these cases.

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WuhanZhengtai Technology Co., Ltd is mainly engaged in the export of fine chemicals, cosmetic raw materials, food additives, pharmaceutical intermediates and other products; Our company is committed to the development of international market, our products are mainly exported to many countries and regions, such as Europe, America, South-east Asia, the Middle East and Africa etc. 

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