Compound Profile

PT 141 (Bremelanotide)

Melanocortin receptor agonist peptide

PT 141 is the research chemical name for bremelanotide, a melanocortin receptor agonist with an actual FDA approved product (Vyleesi) for hypoactive sexual desire disorder in premenopausal women; most gray market marketing (including to men, for erectile dysfunction) extends well beyond that narrow approved indication on much thinner evidence.

Last reviewed:

B Moderate

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PT 141 (Bremelanotide)

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Approved drug exists, but research-chemical product is a separate category

Bremelanotide is FDA-approved as Vyleesi, prescription-only, for hypoactive sexual desire disorder (HSDD) in premenopausal women specifically. PT-141 sold as a research chemical is a different regulatory category, not FDA-approved for any use outside that narrow indication, and is not legally intended for human consumption.

  • Off-label marketing (e.g., male sexual enhancement, general libido) is not backed by the trial data that supports the approved indication.
  • Can transiently raise blood pressure; relevant for anyone with cardiovascular risk factors.
  • This profile is not a self-treatment guide.

Regulatory status

2026 federal and state regulatory context

Last checked 2026 06 30

Vyleesi (bremelanotide) is FDA approved prescription only for HSDD in premenopausal women. RUO labeled PT 141 product is not legally intended for human consumption and is not the same regulatory entity as Vyleesi.

Quick Stats

Evidence level

Moderate evidence

Typical onset

Varies by prep

Safety rating

Use extra caution: Use caution

Best for

Melanocortin Receptor (MC3R/MC4R) Agonism, Central Nervous System Arousal Pathway Activation

Avoid / review if

Uncontrolled Hypertension, Pregnancy/Breastfeeding, Use In Postmenopausal Women Is Not Well Studied

Safety & Cautions

Review before use if any apply: Uncontrolled Hypertension, Pregnancy/Breastfeeding, Use In Postmenopausal Women Is Not Well Studied.

Evidence-based safety

Caution when combined

These pairings share a flagged risk mechanism. They are additive-effect cautions derived from contraindication data, not confirmed clinical interactions. Consult a clinician before combining.

Evidence Summary

B Moderate

Evidence lens

Useful signal, but study design, dose, and population still matter.

ModerateModerate evidence

Human clinical evidence: Present in source signals

Mechanistic / preclinical: Mechanism mappedMelanocortin Receptor (MC3R/MC4R) Agonism · Central Nervous System Arousal Pathway Activation

Research maturity: More interpretablemain contexts: Melanocortin Receptor (MC3R/MC4R) Agonism · Central Nervous System Arousal Pathway Activation

Safety boundary: Safety note availableReview before use if any apply: Uncontrolled Hypertension, Pregnancy/Breastfeeding, Use In Postmenopausal Women Is Not Well Studied.

Evidence Strength

Confidence estimate based on the design quality and consistency of published clinical trials.

Moderate evidence

PT 141 (Bremelanotide) has a moderate evidence evidence rating.

General wellnessGeneral wellness
Effects
2
How evidence grades work

Each grade reflects the strength and consistency of published human evidence — not marketing claims. Grades are based on study count, design quality, effect size, consistency, and recency.

A

Strong

Multiple RCTs, consistent direction, adequate effect size

B

Moderate

Some RCTs or consistent observational data in humans

C

Preliminary / Mixed

Animal or in-vitro only, or conflicting human data

D

Traditional / Theoretical

Traditional use only; no controlled human trials

How PT 141 (Bremelanotide) Works

Simplified mechanism pathway based on preclinical and pharmacological evidence. Does not confirm clinical efficacy.

Mechanism Pathway — How PT 141 (Bremelanotide) Works

How PT 141 (Bremelanotide) WorksPT 141 (Bremelanotide) acts on pathways via melanocortin receptor ((mc3r/mc4r) agonism), leading to melanocortin receptor (mc3r/mc4r) agonism.PT 141 (Bremelanotide)Biological pathwayMelanocortin Receptor(MC3R/MC4R) AgonismMelanocortin Receptor (Mc3r/Mc4r) AgonismObservable outcomeCentral Nervous SystemArousal Pathway Activation
CompoundTarget / ReceptorMechanismEffect / Outcome
Mechanisms & Biological Pathways

Preclinical mechanism details from scientific profiles; these represent plausible pathways but do not guarantee clinical efficacy in humans.

Melanocortin Receptor (MC3R/MC4R) AgonismCentral Nervous System Arousal Pathway ActivationCentral Melanocortin Signaling

Compare & Sourcing

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⚠️ Sourcing Options Disabled for Safety

Direct product recommendations and affiliate links are suppressed for this compound due to its high caution or needs-review safety classification.

Evaluate the safety checks, contraindications, and potential medication interactions below under clinician supervision before use.

Safety first · Harm reduction

This information is educational and not medical advice. Start low, avoid risky combinations, and consult a licensed clinician before making health decisions—especially if you use medications, have diagnosed conditions, or are pregnant/breastfeeding.

Learn how we evaluate confidence, safety, and intensity on the methodology page.

Editorial Review

Checked against primary sources, cited evidence, and contraindication language before publication. Evidence claims, safety language, and affiliate modules are reviewed independently. Not personal medical advice.

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Compound profile context

How to interpret PT 141 (Bremelanotide)

PT 141 dosage by use case, onset and duration, safety limits, and interactions for melanocortin receptor (mc3r/mc4r) agonism, graded against research.… Use this compound profile to understand mechanism, evidence quality, and practical safety context before comparing products or building a stack. A biochemical pathway connection can be useful for discovery, but it is not the same as proven benefit in humans.

When reviewing PT 141 (Bremelanotide), separate the active molecule from the product category around it. Dose form, absorption, extract standardization, medication interactions, and individual sensitivity can change the real-world risk-benefit picture.

For supplement planning, avoid combining multiple compounds with overlapping sedating, stimulating, serotonergic, blood-pressure, anticoagulant, or liver-metabolism effects unless a qualified clinician has reviewed the context.