PT-141, also known as bremelanotide, is a synthetic peptide derived from the alpha-melanocyte-stimulating hormone (α-MSH). It is widely studied for its role in modulating melanocortin receptors, particularly those associated with neurological and physiological responses in laboratory research.

Key Properties

• Melanocortin Receptor Interaction: Investigated for its ability to bind and activate melanocortin receptors (MC1R through MC5R).
• Neurophysiological Modulation: Explored for its role in regulating central nervous system pathways in controlled research environments.
• Cellular Pathway Studies: Studied for its potential influence on cell signalling and receptor activation mechanisms.

Applications in Research

PT-141 is the focus of laboratory research investigating:

• Mechanisms of melanocortin receptor activation and neural pathway interactions.
• Potential effects on physiological responses related to receptor signalling.
• Cellular pathways that may be involved in systemic regulation and energy homeostasis.

Research is conducted in laboratories to expand understanding of PT-141’s biochemical interactions.

Storage and Handling Instructions

• Store PT-141 in its lyophilized form at -4°F (-20°C) or lower.
• Protect from light, moisture, and excessive heat to maintain stability.
• Discard unused or reconstituted solutions promptly in compliance with research protocols.

Safety Information

This product is intended for research purposes. You must:

• Follow institutional guidelines for handling and disposal.
• Use appropriate protective equipment.

Frequently Asked Questions

What is PT-141?
PT-141 is a synthetic peptide derived from α-MSH, studied for its role in activating melanocortin receptors and its potential effects on neural pathways.

How should PT-141 be stored?
Store PT-141 at -4°F (-20°C) in a sealed container protected from light and moisture. Reconstituted solutions should be used promptly following laboratory protocols.

What are the primary research focuses of PT-141?
Research explores its effects on melanocortin receptor activation, neural pathway modulation, and its systemic regulation mechanisms in laboratory settings.