PT-141 vs Melanotan 2: Full Comparison (2026)
PT-141 vs Melanotan-2 comparison: sexual function, tanning, side effects, dosing, FDA status, and pricing.
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PT-141 (bremelanotide) was literally born from Melanotan-2. When researchers discovered that MT-2 caused powerful sexual arousal as a "side effect" during tanning studies, they engineered a modified version to target sexual function specifically — that became PT-141 (Hadley & Dorr, 2006).
Despite sharing a molecular ancestor, these two peptides serve fundamentally different purposes. This guide breaks down exactly where they overlap, where they diverge, and which one fits your goals.
Quick Comparison
| Feature | PT-141 (Bremelanotide) | Melanotan-2 |
|---|---|---|
| Primary use | Sexual function (desire + arousal) | Tanning (with sexual side effects) |
| FDA status | ✅ Approved (HSDD in women) | ❌ Not approved for any indication |
| Receptor targets | MC3R, MC4R (brain) | MC1R, MC3R, MC4R, MC5R (body-wide) |
| Tanning effect | Minimal to none | Significant |
| Sexual enhancement | Strong, targeted | Strong, but untargeted |
| Typical dose | 500 mcg–1 mg (as needed) | 250–500 mcg (daily during loading) |
| Dosing pattern | On-demand before activity | Daily loading → weekly maintenance |
| Nausea severity | Moderate (40%) | Severe during loading (80-90%) |
| Mole/skin changes | No | Yes — requires monitoring |
| Appetite effects | Minimal | Significant suppression |
The Origin Story: How PT-141 Came From MT-2
Understanding the relationship between these peptides explains their differences:
1990s: Researchers at the University of Arizona developed MT-2 as a tanning agent. During Phase I trials, male subjects unexpectedly reported spontaneous erections (Dorr et al., 1996).
1998: Wessells et al. confirmed MT-2's erectogenic properties in a double-blind trial — 8 of 10 men with psychogenic ED developed clinically apparent erections (Wessells et al., 1998).
2000s: Palatin Technologies modified MT-2's structure to create bremelanotide (PT-141), retaining MC3R/MC4R selectivity for sexual function while reducing MC1R activity (tanning) and improving the pharmacological profile.
2019: PT-141 received FDA approval as Vyleesi® for hypoactive sexual desire disorder (HSDD) in premenopausal women, following successful RECONNECT Phase III trials (Kingsberg et al., 2019).
MT-2 never progressed past Phase I for tanning. Its sexual effects remained a "side effect" rather than a feature.
Mechanism of Action: Same Family, Different Targets
Both peptides work through the melanocortin receptor system, but their selectivity profiles are dramatically different.
PT-141: Precision Targeting
PT-141 primarily activates MC3R and MC4R in the hypothalamus — the brain region controlling sexual desire and arousal. This triggers:
- Dopamine release in reward/motivation circuits
- Enhanced neural signaling for sexual desire
- Increased genital arousal through central (not peripheral) mechanisms
This is fundamentally different from PDE5 inhibitors (Viagra, Cialis) which work on blood vessels. PT-141 makes you want sex; PDE5 inhibitors help the mechanics. They can even be combined.
Melanotan-2: Broad Activation

MT-2 activates all five melanocortin receptor subtypes:
- MC1R → Melanin production (tanning)
- MC3R → Energy homeostasis, sexual arousal
- MC4R → Appetite regulation, sexual function, erectile response
- MC5R → Sebaceous gland function
This non-selective binding is why MT-2 produces tanning AND sexual effects AND appetite suppression AND nausea — it's hitting every melanocortin pathway at once.
Sexual Function: Head-to-Head
Both peptides enhance sexual function, but through different approaches:
Desire & Arousal
| Metric | PT-141 | MT-2 |
|---|---|---|
| Onset of sexual effects | 15-30 minutes | 1-4 hours |
| Duration | 4-6 hours | Variable (may persist) |
| Effect on desire | Strong, consistent | Strong but unpredictable |
| Effect on arousal | Central + some genital | Central + genital |
| Clinical evidence | Phase III (1,267 women) | Phase I only |
| Works for women | Yes (FDA-approved) | Anecdotal reports |
For Erectile Dysfunction
PT-141 is the clear winner for ED:
- Purpose-built for the indication
- Works via central arousal (complements PDE5 inhibitors)
- On-demand dosing matches sexual activity timing
- Clinical data in men with psychogenic ED
MT-2 can help ED as a side effect, but:
- Requires daily dosing during loading (not on-demand)
- ED benefits come bundled with tanning, nausea, appetite loss
- No dose optimization for sexual function specifically
- Sexual effects are less predictable in timing
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Tanning: No Contest
PT-141 does not produce meaningful tanning. Its reduced MC1R affinity means melanocyte stimulation is minimal. If tanning is your goal, PT-141 is the wrong peptide entirely.
MT-2 produces significant tanning through MC1R activation:
- Visible results in 1-2 weeks of loading
- Deep tan even with minimal UV exposure
- Requires maintenance dosing to sustain
If you want both tanning and sexual function, MT-2 delivers both. If you want only sexual function, PT-141 is cleaner and safer.
Side Effect Comparison
This is where the two peptides diverge most dramatically:
| Side Effect | PT-141 | MT-2 |
|---|---|---|
| Nausea | 40% (usually mild) | 80-90% during loading (can be severe) |
| Facial flushing | Common, brief | Common, more intense |
| Appetite suppression | Minimal | Significant (MC4R-mediated) |
| Mole changes | No | Yes — requires dermatological monitoring |
| Melanoma concern | No | Theoretical risk (case reports exist) |
| Spontaneous erections | Possible | More common, higher doses |
| Fatigue | Mild | Moderate during loading |
| Injection site darkening | No | Yes |
For a deep dive on every MT-2 side effect with management protocols, see our MT-2 Side Effects Guide.
Safety & Regulatory Status
PT-141: FDA-Approved
PT-141 (Vyleesi®) completed the full FDA approval pathway:
- Two Phase III trials (RECONNECT) with 1,267 women
- Established safety profile over 24-week treatment periods
- Known drug interactions (minimal — low CYP enzyme metabolism)
- Maximum frequency: one dose per 24 hours
MT-2: Unregulated
MT-2 has only completed Phase I clinical trials (safety/tolerability in small groups):
- No Phase II or III efficacy/safety data for tanning
- All available product is unregulated research chemical
- No standardized manufacturing or quality control
- Purity varies significantly between sources
This regulatory gap is the single biggest difference in risk profile between these peptides.
Dosing Comparison
| Parameter | PT-141 | MT-2 |
|---|---|---|
| Starting dose | 500 mcg | 100-250 mcg |
| Standard dose | 500 mcg–1 mg | 250-500 mcg |
| Frequency | As needed (max 1x/24h) | Daily (loading) → 1-2x/week (maintenance) |
| Route | Subcutaneous | Subcutaneous |
| Timing | 30 min before activity | Before bed (to sleep through nausea) |
| Loading required | No | Yes (2-3 weeks) |
| Vial size | 10 mg typical | 10 mg typical |
PT-141's on-demand dosing is a significant practical advantage — you use it only when you need it, rather than committing to a daily loading protocol.
For detailed protocols, see our PT-141 Dosing Guide and MT-2 Dosing Guide.
Which Should You Choose?

Choose PT-141 if:
- Sexual function is your only goal — desire, arousal, or ED
- Safety matters — you want an FDA-approved, clinically tested peptide
- You want on-demand use — take it only when needed
- You don't want tanning — PT-141 won't change your skin color
- Nausea is a concern — PT-141's nausea profile is significantly milder
- You have mole concerns — PT-141 doesn't affect melanocytes
Choose MT-2 if:
- You want tanning as the primary goal — with sexual effects as a bonus
- You want both tanning AND sexual enhancement — MT-2 delivers both
- Cost is a priority — MT-2 is generally cheaper per vial
- You're comfortable with unregulated products — and accept the additional risk
- You've had a dermatological baseline — and will monitor moles regularly
Consider Neither if:
- You have melanoma history — avoid MT-2; PT-141 is fine but won't help tanning
- You're on blood pressure medication — consult your physician first
- You want only tanning without sexual effects — consider Melanotan-1 instead
Frequently Asked Questions
What is the difference between PT-141 and Melanotan 2?
PT-141 is a modified fragment of MT-2 designed specifically for sexual function. PT-141 primarily targets MC3R/MC4R for arousal and desire, with minimal tanning. MT-2 hits all five melanocortin receptors, producing tanning plus sexual side effects, appetite suppression, and nausea.
Can PT-141 be used for tanning?
No — PT-141 has minimal MC1R activity and does not produce meaningful tanning. Use Melanotan-2 or Melanotan-1 for tanning.
Is PT-141 safer than Melanotan 2?
Yes, significantly. PT-141 is FDA-approved with Phase III safety data. MT-2 has only Phase I data and carries additional risks including mole changes, appetite disruption, and higher nausea rates.
Can I use PT-141 and Melanotan 2 together?
Generally not recommended. Both activate MC3R/MC4R, providing redundant stimulation with additive side effects. Use one or the other based on your goals.
Which is better for erectile dysfunction?
PT-141 is the better choice — purpose-built, FDA-studied, on-demand dosing, fewer side effects. MT-2's ED benefits are incidental to its tanning protocol.
How much cheaper is Melanotan 2 vs PT-141?
MT-2 is typically 30-50% cheaper per vial. However, PT-141's on-demand use means you may use fewer total doses over time compared to MT-2's daily loading protocol.
Related Guides
- PT-141 Dosing Guide — Complete bremelanotide protocols
- Melanotan-2 Dosing Guide — Loading, maintenance, and reconstitution
- Melanotan 2 Side Effects — Every MT-2 side effect with management protocols
- Melanotan 1 vs Melanotan 2 — Tanning peptide comparison
- Reconstitution Calculator — Get your dosing right
References
| Citation | Topic | PMID |
|---|---|---|
| Hadley & Dorr, Peptides (2006) | Melanocortin peptide therapeutics, MT-I/PT-141 development | 16412534 |
| Dorr et al., Life Sci (1996) | MT-II Phase I trial, erectogenic discovery | 8637402 |
| Wessells et al., J Urol (1998) | MT-II double-blind ED trial, 8/10 responders | 9679884 |
| Kingsberg et al., Obstet Gynecol (2019) | RECONNECT Phase III, bremelanotide for HSDD | 31599840 |
| Van der Ploeg et al., PNAS (2002) | MC4R role in sexual function and erectile modulation | 12172010 |
For educational and research purposes only. This is not medical advice. PT-141 is FDA-approved for specific indications; Melanotan-2 is not approved for any indication. Consult a healthcare provider.