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PT-141 (Bremelanotide): Melanocortin Pathway Research Guide

A research-focused overview of PT-141 (Bremelanotide), the synthetic melanocortin receptor agonist studied for its central action on arousal pathways. Covers MC3R/MC4R mechanism, how it differs from peripheral PDE5 compounds, and what defines laboratory-grade material.

LyzeLabs Research Team
Published May 14, 2026
8 min read
PT-141 (Bremelanotide): Melanocortin Pathway Research Guide

Disclaimer: This article is for educational and informational purposes only. It does not constitute medical advice. All products referenced are intended for research and laboratory use only and are not approved for human consumption.

PT-141, known in scientific literature as Bremelanotide, occupies a distinct corner of peptide research because it acts where almost nothing else in the sexual-health space does: the central nervous system. Most compounds investigated for arousal work on peripheral blood flow. PT-141 works upstream, on the melanocortin receptor pathway in the brain itself. That single mechanistic difference is why this synthetic heptapeptide has drawn sustained attention from hormone and neuroscience researchers, and why demand for high-purity reference material continues to climb across global laboratories.

Key Takeaways

  • PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide analog of alpha-melanocyte-stimulating hormone (alpha-MSH) studied as a melanocortin receptor agonist.
  • Its functional activity centers on MC3R and MC4R, receptor subtypes densely expressed in hypothalamic and limbic regions tied to motivational behavior in research models.
  • Unlike PDE5-targeting compounds that act peripherally on vascular tissue, PT-141 acts centrally, making it a separate mechanistic class entirely.
  • Reported CAS is 189691-06-3 (base) with a molecular formula of C50H68N14O10, a molecular weight near 1025.2 Da, and an observed half-life of roughly 2.7 hours in published pharmacokinetic data.
  • Laboratory-grade PT-141 should carry a batch-specific Certificate of Analysis (COA) and third-party HPLC verification confirming purity above 99 percent.
  • Lyze Labs ships COA-verified PT-141 worldwide with free, discreet delivery, trusted by 12,000+ researchers across 50+ countries.

What PT-141 Is and How the Mechanism Works

PT-141 is a synthetic analog derived from alpha-MSH, the endogenous peptide hormone that signals through the melanocortin receptor family. Where the parent molecule is broadly active, Bremelanotide was engineered for a narrower, more stable profile. It binds across MC1R, MC3R, MC4R, and MC5R, but the functional activity most relevant to research interest concentrates at MC3R and MC4R.

The mechanistic story is what sets it apart. When PT-141 engages MC4R in neuronal populations, it triggers Gs-protein coupling, activates adenylyl cyclase, and elevates intracellular cAMP, with secondary signaling through phospholipase C and ERK/MAPK cascades. In published cell work, Bremelanotide induces cAMP accumulation in HEK-293 cells expressing the human MC4R, a clean readout that researchers use to confirm receptor engagement.

Because MC3R and MC4R are densely expressed in the paraventricular nucleus of the hypothalamus and surrounding limbic structures, the compound's activity localizes to brain regions associated with motivation and reward in animal models. This is a central nervous system mechanism, not a peripheral one. For researchers mapping the melanocortin system, PT-141 functions as a reliable pharmacological probe of MC4R signaling.

Why Researchers Are Interested

Interest in PT-141 has two roots: its clinical track record and its mechanistic cleanliness. Bremelanotide reached FDA approval in 2019 under the trade name Vyleesi for hypoactive sexual desire disorder in premenopausal women, validated through the Phase III RECONNECT program, two identical randomized, double-blind, placebo-controlled trials enrolling 1,267 participants. Both trials met their coprimary endpoints for desire and distress scores with strong statistical significance.

That clinical validation matters to laboratory researchers because it confirms the target is real and the pharmacology is reproducible. Preclinical investigations have demonstrated in vivo arousal-related responses in both male and female rat models, and earlier work explored Bremelanotide co-administered with peripheral vasodilators, where combined responses exceeded the vasodilator alone in subjects unresponsive to it. For researchers studying the interaction between central drive and peripheral response, that synergy is a productive line of inquiry.

The compound's narrow receptor focus also makes it valuable for isolating MC4R-specific effects from the broader melanocortin system. Researchers comparing melanocortin agonists frequently reference PT-141 alongside related compounds when characterizing receptor selectivity.

How PT-141 Compares to Peripheral-Acting Alternatives

The cleanest way to understand PT-141 is by contrast. PDE5-targeting research compounds act on the nitric oxide pathway in vascular tissue, modulating local blood flow. They never touch the brain's motivational circuitry. PT-141 does the opposite: it activates the upstream neurological pathway and leaves the peripheral vasculature alone.

PropertyPT-141 (Bremelanotide)Peripheral PDE5 Compounds
Primary site of actionCentral nervous system (hypothalamus)Peripheral vascular tissue
Molecular targetMC3R / MC4R melanocortin receptorsPhosphodiesterase type 5 enzyme
Pathway studiedcAMP / ERK-MAPK signalingNitric oxide / cGMP
Compound classCyclic heptapeptideSmall-molecule inhibitor
Research relevanceDesire and arousal circuitryLocalized blood-flow response

This distinction is why the two classes are often studied together rather than as substitutes. They probe different links in the same chain. For broader context on how peptides differ from small molecules in research workflows, the peptide glossary of terms and definitions is a useful companion reference.

Reported Specifications and Physical Profile

Consistent specifications matter when comparing batches across suppliers. The values below reflect figures reported across published chemical and pharmacokinetic sources and should be confirmed against the COA for any specific lot.

SpecificationReported Value
Compound nameBremelanotide (PT-141)
CAS number (base)189691-06-3
Molecular formulaC50H68N14O10
Molecular weight~1025.2 Da
Acetate salt CAS1607799-13-2
Observed half-life~2.7 hours
Receptor activityMC3R, MC4R (functional)
Parent hormonealpha-MSH analog

These figures are reference data for laboratory characterization only. Any analytical work should validate identity and mass against the supplied documentation rather than relying on published averages alone.

What to Look For in Quality and the COA

Peptide quality varies enormously across the market, and PT-141 is no exception. The single most important document is the batch-specific Certificate of Analysis. A credible COA reports HPLC purity, mass spectrometry confirmation of molecular weight, and the specific lot it covers. For PT-141, you want to see purity above 99 percent and a mass result consistent with the ~1025.2 Da figure above.

Third-party verification is the dividing line between a serious supplier and a reseller. In-house numbers can be self-reported; independent HPLC analysis cannot be quietly inflated. Lyze Labs PT-141 is pharmaceutical-grade, third-party HPLC tested, and ships with a COA available per batch confirming purity above 99 percent. Researchers who want to understand the full verification process should read how to verify research peptide purity with a COA, and anyone new to sourcing should review the research peptide scam red flags before buying anywhere.

If a vendor cannot produce a lot-specific COA on request, that absence is itself the answer. Reconstitution and downstream results are only as reliable as the starting material.

Reconstitution and Storage Notes for Research Settings

PT-141 is supplied as a lyophilized powder and requires reconstitution before use in laboratory protocols. In research settings, bacteriostatic water is the standard reconstitution medium, added slowly down the side of the vial rather than directly onto the powder to preserve peptide integrity. The vial should be gently swirled, never shaken, until the solution clears.

Storage discipline protects potency. Lyophilized PT-141 is stable for extended periods when kept frozen and protected from light. Once reconstituted, the solution should be refrigerated and used within a limited window, since peptides in solution degrade faster than in their dry state. For detailed handling, the guide to reconstituting research peptides and the peptide storage and stability guide cover technique and shelf-life in full. Note that these are laboratory handling notes only and not instructions for any other use.

Sourcing PT-141 With Confidence

Global demand for melanocortin and broader peptide research material has surged, and batch availability for high-purity PT-141 moves quickly. Securing current batch pricing while a verified lot is in stock is the practical reality of sourcing reference compounds in a tightening market.

Lyze Labs supplies PT-141 (Bremelanotide) to researchers worldwide from a neutral global position, with free worldwide shipping, discreet packaging, and typical delivery in 7 to 14 days. Every order is backed by third-party HPLC testing and a per-batch COA, and the company is trusted by 12,000+ researchers across 50+ countries. Ordering through WhatsApp is the fastest channel, with support also for Visa, Mastercard, UPI, PayPal, CashApp, bank and wire transfer, and crypto including BTC, USDT, and ETH.

Frequently Asked Questions

What is PT-141 (Bremelanotide) used for in research?

PT-141 is studied as a melanocortin receptor agonist, primarily as a pharmacological probe of MC3R and MC4R signaling in the central nervous system. Researchers investigating arousal and motivational pathways use it to isolate MC4R-specific effects in cell and animal models. All applications are for laboratory and research use only.

How does PT-141 differ from peripheral-acting compounds?

PT-141 acts centrally on melanocortin receptors in the hypothalamus, elevating intracellular cAMP through MC4R. Peripheral PDE5-targeting compounds instead act on the nitric oxide pathway in vascular tissue. They occupy entirely different mechanistic classes, which is why researchers often study them together rather than as substitutes.

What purity should laboratory-grade PT-141 have?

Research-grade PT-141 should be verified above 99 percent purity by HPLC, with mass spectrometry confirming a molecular weight near 1025.2 Da. The most reliable evidence is a batch-specific Certificate of Analysis from third-party testing. Lyze Labs provides a COA per batch on all PT-141 material.

What are the reported chemical specifications of PT-141?

PT-141 has a base CAS of 189691-06-3, a molecular formula of C50H68N14O10, and a molecular weight near 1025.2 Da. The acetate salt form carries CAS 1607799-13-2. Published pharmacokinetic data report a half-life of approximately 2.7 hours.

How should PT-141 be stored in a research setting?

Lyophilized PT-141 should be kept frozen and protected from light, where it remains stable for extended periods. After reconstitution with bacteriostatic water, the solution should be refrigerated and used within a limited window, since dissolved peptides degrade faster than the dry powder. See the storage and stability guide for full handling detail.

How can I order PT-141 from Lyze Labs?

Ordering through WhatsApp is the fastest and preferred channel, and Lyze Labs also accepts Visa, Mastercard, UPI, PayPal, CashApp, bank and wire transfer, and crypto. Shipping is free and discreet worldwide, with typical delivery in 7 to 14 days and a COA included per batch.

Researchers ready to source verified, HPLC-tested material can order PT-141 (Bremelanotide) directly through Lyze Labs. Message us on WhatsApp to confirm current batch availability and secure today's pricing before the lot sells through, every order ships free worldwide with a per-batch COA and purity above 99 percent.

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