Sexual HealthExtensively StudiedFDA Approved

PT-141

Bremelanotide / Vyleesi · Melanocortin MC3R and MC4R agonism in the central nervous system; activates dopaminergic reward pathways and hypothalamic circuits governing sexual behavior; CNS-mediated increase in sexual desire independent of vascular effects

Not medical advice. For educational and research reference only.

Typical Dose

1.75 mg subcutaneous (FDA-approved dose)

Route

Injectable

Cycle

As needed (max 1× per 24 hours)

Storage

Room Temperature (≤77°F)

What is PT-141?

PT-141 (bremelanotide, brand: Vyleesi) is FDA-approved for hypoactive sexual desire disorder (HSDD) in premenopausal women. Unlike PDE5 inhibitors, PT-141 acts centrally on melanocortin receptors in the CNS to increase sexual desire and arousal rather than acting peripherally on blood flow. Administered as a subcutaneous autoinjector 45 minutes before anticipated sexual activity. Banned from 503A compounding pharmacies.

Mechanism of Action

Melanocortin MC3R and MC4R agonism in the central nervous system; activates dopaminergic reward pathways and hypothalamic circuits governing sexual behavior; CNS-mediated increase in sexual desire independent of vascular effects

Target: Melanocortin MC3R and MC4R

Educational reference — not medical advice. Educational research index only — not medical advice. Literature maturity is not a verdict on whether a compound works in people. Community reports are not evidence of efficacy.

Evidence at a glance

Derived · maturity-1.0

Human efficacy is unproven unless an approved label or completed published efficacy program says otherwise. Counts reflect indexed literature volume/kind — never a verdict on effect.

Literature maturity

moderate 61/100

PubMed hits

114

CT.gov trials

10

Strong-human apps

1

Sample papers

8

Sample articles by era

  • pre-20183
  • 2018-20203
  • 2021-20233
  • 2024-20261

Application grades (curated)

  • Human-grade apps1
  • Animal / in-vitro0
  • Mechanistic0

Does literature support studied applications?

Grades reflect cited literature posture — not a treatment recommendation. Community notes are never efficacy evidence.

ApplicationCited evidenceGradeCommunity
Hypoactive sexual desire disorder (premenopausal women) — bremelanotide

Approved bremelanotide (Vyleesi) covers HSDD in premenopausal women; research-chemical forms are distinct.

Strong humanCommunity reports vary; not evidence of efficacy.

Pharmacology

Mechanism of action

  • •Melanocortin MC3R and MC4R agonism in the central nervous system; activates dopaminergic reward pathways and hypothalamic circuits governing sexual behavior; CNS-mediated increase in sexual desire independent of vascular effects
  • •Primary target framing: Melanocortin MC3R and MC4R

Half-life

~2.7 hours

Identity & chemistry

CAS
189691-06-3
Formula
C50H68N14O10
Molar mass
1025.2 Da
InChIKey
FFHBJDQSGDNCIV-MFVUMRCOSA-N

Identity cross-checked with PubChem where available. Compass HTML used only as a bootstrap checklist — not republished as product copy.

Storage & stability

Lyophilized
2–8°C; lyophilized typical shelf 18–24 months
Reconstituted
2–8°C; in-use window often 14–30 days (product-dependent)
Tell-tale degradation
  • !Cloudiness, clumping, or particles after mixing
  • !Discoloration versus the expected clear/colorless (or labeled) solution
  • !Failed or incomplete reconstitution of lyophilized cake

Educational estimates. Prefer product labeling and peptide shelf-life tool.

Lab handling posture

Research / educational handling notes only. Not a substitute for an SDS.

  • •Use PPE appropriate for peptide powder/solution handling
  • •Avoid inhalation of lyophilized powder; handle spills per institutional policy
  • •Do not present research materials as medicines

Sample indexed literature

Research Indications

Sexual FunctionEffective

Research and clinical data supporting effects on sexual response

Libido SupportEffective

Clinical data shows improvements in desire and arousal metrics

Melanocortin ActivityModerate

Acts via central nervous system melanocortin receptor pathways

Research Protocols

These are commonly discussed research protocols — not medical advice. Consult a healthcare provider before use.

GoalDoseFrequencyRoute
Starting DoseLow dosePer protocolVaries
Standard DoseTitratedPer protocolVaries

Peptide & Drug Interactions

Always consult your healthcare provider before combining with other compounds. Use our Interaction Checker for reference.

PDE5 Inhibitors (Sildenafil, Tadalafil)Monitor
Blood Pressure MedicationsCaution
Other Melanocortin AgonistsAvoid
NaltrexoneMonitor

How to Reconstitute & Inject

Use bacteriostatic (BAC) water only. Avoid saline — may cause precipitation. Refrigerate and use within 28 days.

  1. 1

    Remove PT-141 vial from refrigeration and allow to reach room temperature (15–20 minutes)

  2. 2

    Clean vial top with alcohol swab and allow to air dry completely

  3. 3

    Using a sterile syringe, draw the calculated volume of bacteriostatic water (BAC water)

  4. 4

    Inject BAC water slowly down the side of the vial — do not aim directly at the powder

  5. 5

    Gently swirl in circular motions — DO NOT shake vigorously as this degrades the peptide

  6. 6

    Allow 2–3 minutes for full dissolution — solution should be clear and colorless

  7. 7

    Draw calculated dose into an insulin syringe for subcutaneous injection

  8. 8

    Inject into abdomen, thigh, or upper arm. Rotate injection sites to prevent lipodystrophy

  9. 9

    Store reconstituted solution refrigerated (2–8°C) and use within 28 days

What to Expect

Week 1–2

Initial effects and adaptation period. Monitor for any adverse reactions.

Week 2–4

Primary effects begin to manifest. Adjust dosing as recommended by your provider.

Week 4–8

Main therapeutic effects should be established. Assess progress with your provider.

Week 8+

Evaluate results and determine continuation, cycling, or dose adjustments.

Side Effects & Safety

  • Injection site reactions (redness, bruising, mild pain)
  • Potential for allergic reaction — discontinue if rash or hives occur
  • Individual reactions vary — start at the lowest dose and monitor carefully
  • Consult your healthcare provider before use and report any unusual symptoms

PT-141 cannot be prepared by 503A compounding pharmacies. A branded FDA-approved product may exist by prescription. PeptIQ does not sell peptides or list vendors. Talk with a licensed clinician.

FDA Status & Regulatory Info

FDA Approved

PT-141 (bremelanotide, brand: Vyleesi) is FDA-approved for hypoactive sexual desire disorder (HSDD) in premenopausal women. Unlike PDE5 inhibitors, PT-141 acts centrally on melanocortin receptors in the CNS to increase sexual desire and arousal rather than acting peripherally on blood flow. Administered as a subcutaneous autoinjector 45 minutes before anticipated sexual activity. Banned from 503A compounding pharmacies.

Rx Required: Yes
503A Ban: Yes
Telehealth: Available
Full FDA Status Tracker

Frequently Asked Questions

Research References

External links for education only. We do not control third-party content.

Community-reported data

The information below reflects self-reported experiences from PeptIQ app users. It is not clinical evidence and should not replace professional medical advice.

Community Intelligence

What 29 users report

29 community reports

Overall experience

From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.

Favorable 4% · Mixed 3% · Unfavorable overall 93%

Most reported benefits

Benefits users selected when logging a favorable or mixed check-in.

Libido
115
Mood
2

Most logged side effects

Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.

Nausea
38
Headache
37
Injection site irritation
35

Self-reported dose per injection

Median bucket: 2–3 mg · Most common: 2–3 mg

Reports span 0.1 to ≥ 5 mg (open-ended top bucket)

0.1–0.2 mg
1
0.2–0.4 mg
2
0.4–0.6 mg
9
0.6–1 mg
3
1–2 mg
9
2–3 mg
90
5+ mg
1

Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.

How repeat users are trending

Among repeat reporters, 87% said they felt similar to their last entry, 13% more positive, and 0% more negative.

Overall, repeat reporters leaned more positive than their previous entry.

Median gap between entries: 100 days · Based on 23 repeat reporters

Share Your Experience

Rate PT-141 in the PeptIQ app and help the community make informed decisions.

Educational information only

This page is for educational reference. It is not medical or legal advice. PeptIQ does not sell peptides or list vendors. Consult the FDA and a licensed healthcare professional for current regulations and individualized guidance.

PeptIQ app

Log your PT-141 protocol in PeptIQ

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Quick Facts

Half-Life
~2.7 hours
Target
Melanocortin MC3R and MC4R
Route
Injectable
Availability
Pharmacy & Telehealth
Rx Required
Yes
503A Ban
Yes
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Talk with a clinician

PeptIQ is education only. We do not sell peptides or list vendors. Discuss PT-141 with a licensed healthcare provider — not medical advice, not a prescription.

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