Research use only
Structural researchReference entry

MT-2

CATALOG NO.
MT2-10
MOL. WEIGHT
1,024.2
CLASS
Peptide
Computed conformer
Overview

MT-2 is a cyclic lactam heptapeptide analogue of alpha-melanocyte-stimulating hormone (Ac-Nle4-Asp5-His6-D-Phe7-Arg8-Trp9-Lys10-NH2), made by closing a side-chain lactam bridge across the alpha-MSH 4-10 core; the design work that produced this ring reported greater potency and prolonged residual activity than the native hormone in frog and lizard skin bioassays, not in people. Three melanocortin peptides are easily confused and are not the same molecule: MT-2; afamelanotide (melanotan I), a linear alpha-MSH analogue tested in randomized placebo-controlled trials and the only alpha-MSH analogue approved for a medical indication, erythropoietic protoporphyria; and bremelanotide (PT-141), an analogue derived from MT-2 and developed separately for sexual dysfunction. Evidence for those two is not evidence for MT-2. MT-2 itself is not an approved medicine, and its human record stops at three small early-phase studies run by a single University of Arizona group between 1996 and 2000.

Research-use-only note

Information on this page is provided for laboratory research reference. The compound is not a drug, supplement, or medical product, and is not for human or veterinary use, ingestion, or consumption.

Molecular characteristics
Catalog no.MT2-10
Research areaStructural
ClassPeptide
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
Length7 aa
Molecular weight1,024.2 g/mol
Molecular formulaC50H69N15O9
Measured purity99.756% · report #137015
FormLyophilized research material
AppearanceWhite to off-white powder
UseFor laboratory research use only
VerificationReference specifications pending COA verification
COA statusPending authentic product-specific COA
Measured results
Measured HPLC purityreport #137015
98.099.0100.0
  • #137015 · 10 mg99.756%

Each result applies to the tested sample shown, not to every catalog strength or lot.

Sequence
NleDHFRWKAcNH₂
Nle
Norleucine — Straight-chain leucine isomer; a non-oxidisable methionine surrogate.
Phe
D-Phenylalanine
How it works

MT-2 is a potent but unselective agonist across the human melanocortin receptors; the lactam cyclization holds the alpha-MSH pharmacophore in its active conformation, and replacing that bridge with other linkers shifts receptor affinity and can produce the hMC1R functional selectivity the parent peptide lacks. MC1R activation on melanocytes stimulates eumelanin production and skin pigmentation independent of sun exposure, while central MC3R/MC4R activation is the pathway invoked for the erectile, appetite and body-composition effects reported in the early human studies and in rodents; the appetite and body-composition work is rodent-only and used infusion directly into the brain.1,5,8,9,10

What the research shows9 findings · 22 sources · 4 from clinical trials

Skin & hair

In a 1996 single-blind, alternating-day, placebo-controlled pilot phase I study in 3 healthy male volunteers, 2 of the 3 had increased pigmentation of the face, upper body and buttock on both quantitative reflectance and visual assessment, measured one week after two weeks of subcutaneous dosing ended.2

Clinical trialPhase Phase I · 3 participants · 2 weeks dosing, assessed 1 week after3 healthy male volunteers, single-blind alternating-day placebo-controlled dose escalation

Vials sold as MT-2 skin-tanning product by three online shops were assayed by LC-UV-MS/MS, using methods validated against guidelines for active substances in authorised medicines. Total peptide per vial ranged from 4.32 to 8.84 mg against a labelled 10 mg at every shop, and vials from two of the three shops carried unidentified impurities of 4.1 to 5.9 percent. These are label-versus-content figures.11

Lab studyPhase not applicable · 3 studies · not applicableanalytical chemistry of illicitly sold internet-sourced MT-2 vials from three shops

In a 2026 single-patient case report with three months of follow-up, a person who self-injected MT-2 over a 64-day period for tanning had brown pigmentation on the attached gingiva of both arches and on both buccal mucosae; one month after stopping, the buccal pigmentation had nearly disappeared, while at three months the gingival pigmentation persisted at reduced intensity.9

Clinical trialPhase case report, not a trial · 1 participants · 64 days of use, 3 months follow-upsingle-patient case report, intraoral examination and follow-up

A qualitative study extracted 623 discussion entries from 205 contributors on public UK and Ireland forums between January 2016 and October 2017. Reported motivations for MT-2 use included a tanned appearance ahead of sun holidays and fitness or bodybuilding competitions; themes also covered misinformation, sunbed use, self-reported side effects and practices the authors judged concerning. It measured no clinical outcome.12

Evidence reviewPhase not applicable · 205 studies · posts from January 2016 to October 2017inductive thematic analysis of public online forum posts; not a clinical study

Libido & sexual health

In a 1998 double-blind, placebo-controlled crossover study in 10 men with erectile dysfunction of no known organic cause, RigiScan monitoring across a 6-hour window recorded mean tip rigidity above 80 percent lasting 38.0 minutes after MT-2 versus 3.0 minutes after vehicle placebo (p=0.0045); clinically apparent erections developed in 8 of the 10 men.3

Clinical trialPhase early-phase controlled clinical trial · 10 participants · 6-hour monitoring per injection10 men with psychogenic erectile dysfunction, double-blind placebo-controlled crossover

In a 2000 double-blind, placebo-controlled crossover study in 10 men whose erectile dysfunction had organic risk factors, run by the same University of Arizona group, mean duration of tip rigidity above 80 percent was 45.3 minutes after MT-2 versus 1.9 minutes after vehicle (p=0.047); subjectively reported erections followed 12 of 19 MT-2 injections versus 1 of 21 placebo injections, and self-rated sexual desire was significantly higher after MT-2 than placebo.4

Clinical trialPhase early-phase randomized controlled trial · 10 participants · 6-hour monitoring per injection10 men with organic-risk erectile dysfunction, double-blind placebo-controlled crossover

In 14 ovariectomized female Long-Evans rats, intravenous MT-2 given before 30-minute paced mating tests significantly increased hops, darts and ear wiggling versus saline in the 7 rats primed with estradiol benzoate plus progesterone, but did not alter pacing or lordosis; in the 7 rats primed with estradiol alone it altered none of the measured behaviours.13

Animal studyPhase preclinical · 14 studies · 30-minute mating testsovariectomized Long-Evans rats, paced mating test, each female received all treatments

Fat loss & metabolism

In male Wistar rats held four weeks on free-choice diets, MT-2 infused directly into the brain's lateral ventricle suppressed caloric intake more in rats given chow plus saturated fat than in rats on chow alone, chow plus liquid sugar, or chow plus fat plus sugar; the fat component was suppressed most and the sugar component least, tracking diet composition rather than body-weight gain. Rodent, brain-infusion result only.10

Animal studyPhase preclinical · 4 weeks of diet before testingmale Wistar rats on free-choice diets, MT-2 into the lateral ventricle versus vehicle

In rats given MT-2 by continuous infusion into the brain versus vehicle, with a third group pair-fed to match MT-2 intake, MT-2 produced rapid and sustained fat-mass loss that pair-feeding did not reproduce; MT-2 rats held their lean-to-fat mass ratio while pair-fed rats transiently lost theirs, and long-term body-mass loss was independent of the initial hypophagia. Rodent, brain-infusion result only.14

Animal studyPhase preclinical · body composition assessed biweeklyrats, central MT-2 infusion versus vehicle and pair-fed controls
Reported adverse events

What investigators recorded alongside the results above, at the rates their papers state.

Melanoma, cutaneous and mucosal. In one case report a 20-year-old woman with Fitzpatrick type II skin had a gluteal melanoma excised three months after a 3-to-4-week course of MT-2 self-injection taken to augment sunbed tanning. A second report describes melanoma in situ associated with an injectable melanotropic peptide sold as 'melanotan', the specific analogue not named in the record. A third describes a 22-year-old woman with a maxillary mucosal malignant melanoma after using an MT-2 nasal spray for tanning, treated by resection and ongoing immunotherapy.15,16,17

as reported in individual case reports; there is no incidence rate for any of this, and causality is established in none of them

Clinical trial

Eruptive and atypical (dysplastic) nevi, and darkening or growth of existing moles. A review of unregulated use of the alpha-MSH analogues melanotan I and II found melanocytic change in existing moles and newly emerging dysplastic nevi to be the chief reported cutaneous complications, and counted four case reports of melanoma emerging from existing moles during or shortly after melanotan use while stating that conclusive evidence linking them is lacking. A separate case report describes a 40-year-old man with prior melanoma and multiple dysplastic nevi who self-administered a synthetic alpha-MSH peptide, which the report does not identify as MT-2, and developed crops of clinically and histopathologically atypical nevi that lightened and lost growth features after he stopped.7,18

as reported; described in the review as the chief cutaneous complication in the case literature, with no rate given and no causality established. The review covers melanotan I and melanotan II together and does not separate them

Evidence review

Rhabdomyolysis with sympathomimetic toxicity and renal injury. A 39-year-old man who self-injected internet-purchased MT-2, in a single quantity he described as several times his usual starting amount and later confirmed as MT-2 by mass spectrometry, presented with tachycardia, hypertension, mydriasis, diaphoresis and tremor, with creatinine 2.25 mg/dL on presentation and creatine kinase rising to 17,773 IU/L twelve hours later; he was discharged from intensive care after three days. A separate case report with literature review describes a renal infarction the authors considered most likely attributable to MT-2.19,20

as reported in individual case reports; causality is not established in either, and the second is framed by its own authors as a possible cause

Clinical trial

Priapism. A patient presented to the emergency department of a tertiary urology centre with acute low-flow priapism after abdominal subcutaneous injection of melanotan, which the report names without specifying the analogue. He was managed with cavernosal aspiration, irrigation and intracavernosal phenylephrine, avoided surgical shunting, and had not recovered erectile function at four-week follow-up.21

as reported in a single case report; causality is not established, and the analogue used is not specified in the record

Clinical trial

Posterior reversible encephalopathy syndrome. A report indexed by PubMed as a case report and letter is titled 'Melanotan and the posterior reversible encephalopathy syndrome'. It carries no abstract in PubMed, and its title names 'melanotan' rather than melanotan II, so which analogue was involved cannot be determined from the record. Nothing beyond that reported association is asserted here.22

as reported in a single published case report that has no abstract; causality is not established and the analogue is not specified

Clinical trial

Acute symptoms in the early-phase human studies. Nausea, severe after 4 of 19 MT-2 injections in the 2000 organic-erectile-dysfunction crossover; a stretching-and-yawning complex; decreased appetite in the 1998 psychogenic crossover; and WHO grade II somnolence and fatigue in one of the two volunteers escalated to the highest level in the 1996 phase I study.2,3,4

as reported; nausea and the stretching-and-yawning complex were more frequent after MT-2 than after placebo in both 10-man crossover studies

Clinical trial
Sources
  1. 1.Potent and prolonged acting cyclic lactam analogues of alpha-melanotropin: design based on molecular dynamics. · Journal of medicinal chemistry · 1989 · PMID 2555512
  2. 2.Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study. · Life sciences · 1996 · PMID 8637402
  3. 3.Synthetic melanotropic peptide initiates erections in men with psychogenic erectile dysfunction: double-blind, placebo controlled crossover study. · The Journal of urology · 1998 · PMID 9679884
  4. 4.Effect of an alpha-melanocyte stimulating hormone analog on penile erection and sexual desire in men with organic erectile dysfunction. · Urology · 2000 · PMID 11018622
  5. 5.Melanocortin peptide therapeutics: historical milestones, clinical studies and commercialization. · Peptides · 2006 · PMID 16412534
  6. 6.Afamelanotide for Erythropoietic Protoporphyria. · The New England journal of medicine · 2015 · PMID 26132941
  7. 7.Risks of unregulated use of alpha-melanocyte-stimulating hormone analogues: a review. · International journal of dermatology · 2017 · PMID 28266027
  8. 8.CLIPSing Melanotan-II to Discover Multiple Functionally Selective hMCR Agonists. · Journal of medicinal chemistry · 2022 · PMID 35188390
  9. 9.Changes in Oral Mucosa Associated with Melanotan II Injections: A Case Report. · Life (Basel, Switzerland) · 2026 · PMID 41752902
  10. 10.Inhibitory Effect of the Melanocortin Receptor Agonist Melanotan-II (MTII) on Feeding Depends on Dietary Fat Content and not Obesity in Rats on Free-Choice Diets. · Frontiers in behavioral neuroscience · 2015 · PMID 26733840
  11. 11.Identification and characterization by LC-UV-MS/MS of melanotan II skin-tanning products sold illegally on the Internet. · Drug testing and analysis · 2015 · PMID 24771717
  12. 12.Melanotan II User Experience: A Qualitative Study of Online Discussion Forums. · Dermatology (Basel, Switzerland) · 2021 · PMID 34464955
  13. 13.The melanocortin agonist, melanotan II, enhances proceptive sexual behaviors in the female rat. · Pharmacology, biochemistry, and behavior · 2006 · PMID 17113634
  14. 14.Activation of the central melanocortin system in rats persistently reduces body and fat mass independently of caloric reduction. · Canadian journal of physiology and pharmacology · 2018 · PMID 29131966
  15. 15.Melanoma associated with the use of melanotan-II. · Dermatology (Basel, Switzerland) · 2014 · PMID 24355990
  16. 16.Melanotan-associated melanoma in situ. · The Australasian journal of dermatology · 2012 · PMID 22724573
  17. 17.Melanotan II nasal spray: a possible risk factor for oral mucosal malignant melanoma? · International journal of oral and maxillofacial surgery · 2025 · PMID 40210573
  18. 18.alpha-Melanocyte-stimulating hormone-induced eruptive nevi. · Archives of dermatology · 2009 · PMID 19380666
  19. 19.Melanotan II injection resulting in systemic toxicity and rhabdomyolysis. · Clinical toxicology (Philadelphia, Pa.) · 2012 · PMID 23121206
  20. 20.Melanotan II: a possible cause of renal infarction: review of the literature and case report. · CEN case reports · 2020 · PMID 31953620
  21. 21.Melanotan-induced priapism: a hard-earned tan. · BMJ case reports · 2019 · PMID 30796078
  22. 22.Melanotan and the posterior reversible encephalopathy syndrome. · Annals of internal medicine · 2013 · PMID 23648958
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