Peptide database / Melanocortin

Melanotan-2

An unapproved ring-shaped alpha-MSH analog that darkens skin and causes erections; tested in a few small 1990s studies, never approved.

Research chemical WADA prohibited B Evidence At least one human randomized trial

Also called Melanotan II, MT-II, MT2, Ac-Nle4-c[Asp5, D-Phe7, Lys10]-alpha-MSH(4-10)-NH2, Barbie drug, Tanning injection

All peptides Last reviewed October 13, 2026
Legal status Research chemical Banned in sport (WADA)
Evidence grade B At least one human randomized trial
Human studies 5 published, approximate count
Half-life Not characterized in humans time for levels to halve
Route studied Subcutaneous injection (published studies) plus intranasal spray (sold online, never studied)
What it is

Melanotan-2 is a 7-amino-acid ring-shaped peptide built at the University of Arizona in 1989 as a shorter, tougher copy of alpha-MSH, the hormone that darkens skin. Unlike melanotan-1, it switches on several melanocortin receptors at once: MC1R on pigment cells, which tans the skin, and MC3R and MC4R in the brain, which cut appetite and trigger erections and sexual arousal.

The human data are thin. A 3-man pilot in 1996 found it tanned the face and upper body after 5 low doses, and the men also had spontaneous erections, bouts of yawning and stretching, and mild nausea. Two 10-man placebo-controlled crossover studies in 1998 and 2000 then tested it for erectile dysfunction: erections with tip rigidity over 80% lasted 38 to 45 minutes on the drug versus 2 to 3 minutes on placebo, but some men had severe nausea. Development moved to bremelanotide (PT-141), a close relative of MT-II that became the approved drug Vyleesi. Melanotan-2 itself was never approved anywhere.

Read the full overview 1 more

Today it is sold online as a tanning injection or nasal spray. Dermatologists have published case reports of new and darkening moles, several melanomas, priapism, rhabdomyolysis and a kidney infarction in people using these products. None of those reports proves the drug caused the problem, but no one has ever studied the long-term safety of repeated use, and the vials are unregulated.

Structure 7 residues
1. Nle Nle 2. Aspartic acid D 3. Histidine H 4. D-Phenylalanine dF 5. Arginine R 6. Tryptophan W 7. Lysine K N C
  • Hydrophobic
  • Positive charge
  • Negative charge
  • Non-standard
Sequence
Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-NH2
Length
7 amino acids
Molecular weight
1024.2 g/mol
Origin
Synthetic cyclic heptapeptide based on alpha-MSH residues 4 to 10, closed by a lactam bridge between Asp5 and Lys10, with norleucine at position 4 and D-phenylalanine at position 7; designed at the University of Arizona (1989)
Mechanism

How Melanotan-2 works

What it binds to, and what happens inside the body after that, step by step.

Outside the cell Inside the cell
Target Melanocortin receptors MC1R, MC3R, MC4R, MC5R (non-selective agonist)

MT-II is a non-selective agonist at melanocortin receptors MC1R, MC3R, MC4R and MC5R. At MC1R on melanocytes it raises cAMP and eumelanin production, darkening the skin. It crosses into the brain, where MC4R activation in the hypothalamus and spinal pathways triggers erections, sexual arousal, yawning and reduced appetite. That receptor spread is why its side effects are broader than afamelanotide's.

  1. 1 Injection or nasal absorption Given under the skin in the published studies. Nasal sprays sold online have no published absorption data.
  2. 2 MC1R in skin Activates MC1R on melanocytes, raising cAMP and eumelanin output so skin, moles and freckles darken.
  3. 3 MC4R in the brain Reaches the hypothalamus and acts on MC4R, which drives erections, sexual desire, stretching and yawning, and lowers appetite.
  4. 4 Visible effects Erections started within hours of a dose in the 1990s studies; tanning showed up about a week after a course of injections.
The research

What the studies show

Human results and animal results are kept apart below. A result in rats tells you a mechanism is plausible. It does not tell you what happens in a person.

B Evidence

Humans: two 10-man placebo-controlled crossover trials show it reliably triggers erections, and a 3-man pilot showed skin darkening after a few low doses. That is the entire controlled human dataset, all from one Arizona group in 1996 to 2000, all short-term. Everything else in humans is case reports of harm in people using unregulated products. Appetite and weight effects come from rodent studies only.

How far the evidence reaches Highest rung: Randomized trials
  1. Cell studies In a dish None listed
  2. Animal studies Rodents and other models None listed
  3. Small human studies Open-label, case series 3 key studies below
  4. Randomized trials Placebo-controlled RCTs, meta-analyses 2 key studies below
  5. Regulatory approval Not approved No
Preclinical: tells you a mechanism is plausible Human: tells you what happened in people (5 published studies, approx.)

In people 5

Randomized trial 1998

Synthetic melanotropic peptide initiates erections in men with psychogenic erectile dysfunction (Wessells et al., J Urol)

10 men with psychogenic erectile dysfunction, double-blind placebo crossover

8 of 10 men had erections; tip rigidity over 80% lasted a mean 38.0 minutes on MT-II vs 3.0 minutes on placebo (P=0.0045).

Read the study
Randomized trial 2000

Effect of an alpha-MSH analog on penile erection and sexual desire in men with organic erectile dysfunction (Wessells et al., Urology)

10 men with erectile dysfunction and organic risk factors, double-blind placebo crossover

Erections followed 12 of 19 MT-II injections vs 1 of 21 placebo doses; 4 of 19 injections caused severe nausea.

Read the study
Human, open-label 1996

Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide, in a pilot phase-I clinical study (Dorr et al., Life Sciences)

3 healthy men, single-blind alternating-day placebo design

Two of three men had measurable darkening of the face, upper body and buttocks a week after dosing ended; spontaneous erections came and went for 1 to 5 hours after doses, and mild nausea occurred at most dose levels.

Read the study
Show all 5 studies
Case series 2012

Melanotan II injection resulting in systemic toxicity and rhabdomyolysis (Nelson et al.)

One 39-year-old man who injected 6 mg of internet-bought MT-II

He developed racing heart, agitation and muscle breakdown with CK peaking at 17,773 IU/L and temporary kidney injury; lab testing confirmed the product was MT-II.

Read the study
Case series 2014

Melanoma associated with the use of melanotan-II (Hjuler and Lorentzen)

One 20-year-old woman with fair skin who used MT-II with sunbeds

A melanoma was diagnosed on the buttock 3 months after a 3 to 4 week course of self-injected MT-II combined with sunbed use.

Read the study
Gaps in the research

What nobody has measured yet

These are questions the published research has not answered.

  1. 01 Whether repeated MT-II use raises melanoma risk; no cohort or controlled study exists.
  2. 02 Basic human pharmacokinetics: half-life, absorption and clearance have never been published.
  3. 03 Long-term safety of any kind; the longest controlled exposure was 2 weeks.
  4. 04 Whether nasal sprays sold online deliver any drug at all.
  5. 05 The identity, purity and dose of internet products; independent testing of melanotan vials has not been systematically published.
  6. 06 Whether it changes appetite or body weight in humans; that evidence is from rodents.
  7. 07 Effects in women; all controlled studies enrolled men.
History

Melanotan-2 from discovery to today

1989202637 years of research history
  1. 1989Al-Obeidi, Hruby and Hadley at the University of Arizona publish cyclic lactam alpha-MSH analogs, including the compound later called Melanotan-II.
  2. 1996First human pilot study: 3 men show skin darkening plus spontaneous erections, yawning and nausea.
  3. 1998Placebo-controlled crossover trial shows MT-II triggers erections in men with psychogenic erectile dysfunction.
  4. 2000Second crossover trial extends the erection finding to men with organic risk factors; development shifts to bremelanotide (PT-141).
  5. 2012A case report describes rhabdomyolysis and kidney injury after an internet-bought MT-II injection, adding to earlier reports of changing moles in users; priapism, melanoma and kidney infarction reports follow.
  6. 2019Bremelanotide, a close MT-II relative, is approved by FDA as Vyleesi; MT-II itself stays unapproved.
  7. 2023FDA places melanotan II in 503A Category 2, citing immunogenicity and case reports including melanoma and priapism.
  8. 2026Nomination withdrawn and FDA removes MT-II from Category 2 in April; it is slated for an advisory committee review before the end of February 2027.
Approval or regulatory milestoneResearch milestone
Pharmacokinetics

How long it stays in the body

Half-life
Not characterized in humans
Routes studied
Subcutaneous injection (published studies), Intranasal spray (sold online, never studied)
Bioavailability
Unknown in humans. The 1990s studies used subcutaneous injection and did not report plasma levels.
Notes
No human pharmacokinetic study has been published. In the 1996 pilot, erections came on within hours of a dose and lasted 1 to 5 hours, and tanning appeared about a week after the last dose. Its relative bremelanotide has a labeled half-life of about 2.7 hours, but that does not transfer directly because the molecules differ at the C-terminus.

No human half-life has been published for Melanotan-2, so we do not draw a clearance curve. Half-lives quoted online for it are usually estimates from animal data.

Members

Doses used in published studies

This table records the doses that trials and approved labels used, with the source for each row. It is a record of research, not a recommendation, and it is open to free members.

Doses used in published research and approved labels3 rows
Checking membershipEach row names the trial or label, the dose, route, frequency, duration and a link to the source. Free account, no card.
Safety

Side effects, higher-risk groups and interactions

5Commonroughly 1 in 10 or more
1Uncommonroughly 1 in 100 to 1 in 10
2Rareunder 1 in 100
1Frequency unknownnot measured in trials
EffectCommonUncommonRareUnknown
NauseaReported at most dose levels in every published study; 4 of 19 injections caused severe nausea in the 2000 trial.Common
Spontaneous erectionsReported in the 1996 pilot, coming on with yawning and stretching and recurring for 1 to 5 hours after a dose.Common
Yawning and stretchingA stretching and yawning complex came just before erections in the 1990s studies.Common
Reduced appetiteDecreased appetite was reported more often after MT-II than placebo in the 1998 trial.Common
Darkening and new molesMultiple case reports describe eruptive, atypical or darkening moles in users; the existing mole count and sun habits of users make cause hard to separate.Common
Sleepiness and fatigueGrade II somnolence and fatigue at 0.03 mg/kg in one of two men in the 1996 pilot.Uncommon
PriapismErections lasting hours that needed emergency treatment have been reported in case reports, including after overdose.Rare
Rhabdomyolysis, kidney injury, kidney infarctionIsolated case reports in people using internet-bought MT-II; not seen in the controlled studies.Rare
MelanomaAt least four case reports of melanoma during or after use. Whether MT-II raises melanoma risk has never been studied.Frequency unknown
Groups with specific risks
  • Personal or family history of melanoma, atypical mole syndrome, or many moles.
  • Pregnancy and breastfeeding: no human data.
  • History of priapism or conditions that raise priapism risk such as sickle cell disease.
  • Uncontrolled high blood pressure or heart disease: the Vyleesi label for its relative bremelanotide lists these as contraindications because each dose briefly raises blood pressure; MT-II's cardiovascular effects were never studied.
  • Competing athletes, because it falls under WADA's S0 ban on unapproved drugs.
Interactions
  • PDE5 inhibitors (sildenafil, tadalafil): combined erectile effects raise the chance of prolonged erection; never studied together.
  • Bremelanotide (PT-141) or afamelanotide: same receptor family, so effects stack; no data on combined use.
  • Tanning beds and heavy sun exposure: case reports of melanoma and changing moles mostly involve MT-II combined with sunbeds.
  • Oral naltrexone: the Vyleesi label says bremelanotide can sharply lower naltrexone blood levels and may slow stomach emptying; whether MT-II does the same is unknown.

Which symptoms are expected and which mean stop and get help: side effects and red flags.

Claims checked

What people say online, checked against the studies

Tap a claim to see what the studies found.

The claim"Melanotan 2 lets you tan without sun damage."Not supportedThe evidence does not back this

MT-II darkens skin without UV in small studies, but no study has shown it protects against sunburn, skin aging or cancer. Most users combine it with sunbeds, and that combination appears in most of the melanoma case reports.

The claim"Melanotan 2 causes melanoma."MixedSome studies agree, some do not

There are case reports of melanoma and fast-changing moles in users, and FDA cited melanoma when restricting compounding. Case reports cannot prove cause, and no study has measured risk. The honest answer is that a real risk has not been ruled out.

The claim"It works as a libido booster."SupportedHuman evidence backs this

Two small placebo-controlled trials in men showed it triggers erections and raised self-rated sexual desire. Its relative bremelanotide is approved for low desire in premenopausal women. Neither fact means MT-II is safe for routine use.

The claim"Melanotan 2 is an appetite suppressant that helps weight loss."UntestedNobody has measured this in people

Reduced appetite was reported as a side effect, and rodent studies show MC4R activation cuts food intake, but no human study has measured weight change.

The claim"The nasal spray is a safer, needle-free option."UntestedNobody has measured this in people

No study has tested nasal MT-II for absorption, dose or safety. One 2025 case report raised oral mucosal melanoma in a nasal spray user, without proof of cause.

The claim"Melanotan 2 and PT-141 are the same thing."MixedSome studies agree, some do not

They are close relatives: bremelanotide is MT-II with a free acid instead of an amide at the C-terminus. Bremelanotide went through full Phase 3 trials and FDA approval; MT-II never did.

Untested pairings

Combinations people discuss

These pairings come up often. Almost none have been tested together in a trial, and the evidence note on each says so plainly.

Melanotan 2 with sunbed sessions

Users combine injections with sunbeds or sun exposure to speed up the tan, since MT-II amplifies the pigment response to UV.

EvidenceNo study has tested MT-II with sunbeds. Most published melanoma and atypical mole case reports involve exactly this combination, and sunbeds alone raise melanoma risk.

Melanotan 2 with PT-141

Discussed online for combined tanning and libido effects.

EvidenceNever studied. Both act on the same receptors, so nausea, blood pressure effects and prolonged erections would be expected to add up.

Handling

Storage and stability

Dry powder (lyophilized)

No approved product exists, so there is no labeled storage. Published stability data for research-grade MT-II powder are not available.

Mixed with water (reconstituted)

No published stability data exist for reconstituted MT-II.

Guide Reconstitution and storage, explainedMembers Bacteriostatic water, fridge vs freezer, and how fast peptides break down.
Keep reading

Related peptides

The Staate peptide brief

New Melanotan-2 research, explained when it is published

One email when a trial reads out, a label changes or the FDA acts on a peptide. Free, no selling of peptides, unsubscribe any time.

Frequently asked questions
Is Melanotan 2 legal?
It is not approved as a drug anywhere. In the US it cannot be legally marketed for human use, and it is not on the list of substances pharmacies can compound. Several countries have issued warnings against buying tanning injections online.
What is the difference between Melanotan 1 and Melanotan 2?
Melanotan 1 (afamelanotide) mostly acts on the skin's MC1 receptor and is an approved drug for a rare light-sensitivity disorder. Melanotan 2 acts on several melanocortin receptors including MC4R in the brain, so it also causes erections, nausea and appetite loss, and it was never approved.
Why does Melanotan 2 cause nausea and erections?
It reaches the brain and switches on the MC4 receptor, which controls sexual arousal, erections and appetite. Nausea was the most common side effect in every published study.
Can Melanotan 2 cause skin cancer?
No study has measured that risk. Dermatologists have reported new and changing moles and several melanomas in users, and FDA cited melanoma when it restricted compounding. Anyone who has used it should get changing moles checked.
Is Melanotan 2 banned for athletes?
It is not named on the WADA list, but WADA's S0 rule bans any substance with no approval for human therapeutic use, which covers MT-II.
Do melanotan tans fade?
Yes. In the Arizona studies, darkening was measured about a week after the last dose; with melanotan-1 it peaked at 1 week and was still visible 3 weeks later. Nobody has published how long an MT-II tan lasts after repeated use.