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PT 141 10mg

PT 141 10mg

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide analog of α-MSH that acts as a melanocortin receptor agonist, studied primarily for MC4R-mediated signaling in the central nervous system. Supplied as a ≥99% HPLC-verified lyophilized powder for laboratory research use only.

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Compound Information

Technical specifications


Molecular Profile

What Is PT-141?

TypeMelanocortin Receptor Agonist (Cyclic Peptide)
CAS Number189691-06-3
Molecular Weight1025.16 g/mol
SynonymsBremelanotide / Vyleesi / Melanotan II metabolite
Amino Acids7 AA (Cyclic lactam heptapeptide)
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
FormulaC50H68N14O10

Storage Requirements

Stability Information

Lyophilized powder; keep sealed, dry, and protected from light
Cyclic structure confers good stability relative to linear analogs
Aliquot after reconstitution; avoid repeated freeze–thaw cycles

Lyophilized Powder

-20°C preferred; 2–8°C for short-term handling

Reconstituted

2–8°C


About PT-141

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide analog of alpha-melanocyte-stimulating hormone (α-MSH), structurally derived from Melanotan II. Its cyclic lactam architecture confers greater metabolic stability than linear melanocortin peptides while preserving receptor affinity. It acts as an agonist across several melanocortin receptor subtypes, with research interest centered on MC4R and MC3R signaling in the central nervous system. This makes PT-141 a reference compound for investigating melanocortin pathway activation, receptor-subtype selectivity, and downstream neural signaling. Supplied as a high-purity lyophilized powder for reproducible in-vitro and approved in-vivo work. This product is for laboratory research and development purposes only and must be handled by qualified professionals. Not for human, therapeutic, or diagnostic use.


Research Highlights

Melanocortin Receptor Agonism

Engages multiple melanocortin receptor subtypes, making it a useful probe for mapping pathway activation across the family.

MC4R Signaling Studies

Research interest centers on MC4R engagement in the central nervous system and its downstream neural signaling effects.

Cyclic Lactam Stability

The constrained ring structure resists enzymatic degradation better than linear analogs while retaining receptor affinity.

Receptor-Subtype Selectivity

Its cross-subtype activity makes it a common comparator in binding assays that characterize newer, more selective ligands.

Structural Analog Reference

Derived from Melanotan II, giving researchers a defined structural point of comparison within the melanocortin peptide family.

≥99% HPLC Purity

Every batch is HPLC-verified and supplied lyophilized, ensuring reproducible results across long study timelines.

Product Specifications

Molecular Formula
C50H68N14O10
Molecular Weight
1025.16 g/mol
CAS Number
189691-06-3
Sequence
Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Purity
≥99% (HPLC verified)
Form
Lyophilized powder
Appearance
White to off-white powder
Solubility
Soluble in water, bacteriostatic water
Storage
-20°C (lyophilized), 2–8°C (reconstituted)

Research Studies

Frequently Asked Questions

What is PT-141?

PT-141, also known as Bremelanotide, is a synthetic cyclic heptapeptide analog of α-MSH that acts as a melanocortin receptor agonist.

How does it relate to Melanotan II?

PT-141 is structurally derived from Melanotan II and shares its cyclic lactam core, making the two useful structural comparators within the melanocortin peptide family.

Why is the cyclic structure significant?

The constrained lactam ring resists enzymatic degradation more effectively than a linear sequence, giving the peptide greater metabolic stability while preserving receptor affinity.

Is this product approved for human use?

No. This product has not been evaluated by the FDA and is strictly intended for research and development purposes by qualified professionals only. It is not for human, therapeutic, or diagnostic use.

PT-141 molecular structure

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