Everything below concerns cyclic heptapeptide. We keep the language plain, cite what the science says, and separate well-supported claims from open questions.
Last reviewed on 2025-09-14. Where a claim depends on a specific study, the study is described rather than over-claimed.
Early published reports described melanotan-2 as a tanning agent without sun protection, which means darkening is not the same as protection against ultraviolet radiation. Later studies explored the peptide in erectile dysfunction, hemorrhagic shock, and some skin conditions. No regulator in the United States or Europe has approved it for clinical use. Many products labelled melanotan-2 are sold without approval and their identity and purity are unverified. Its long-term safety in humans remains an open question.
Melanotan-2, also written Melanotan II, is a synthetic cyclic heptapeptide designed as an analogue of alpha-melanocyte-stimulating hormone. Its sequence is Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2, and the lactam bridge between the aspartate and lysine side chains constrains the peptide into a ring. This structural change increases receptor affinity and metabolic stability relative to the native hormone. The compound was created in the 1980s as a research tool for studying pigmentation biology.
Receptor binding at MC1R on melanocytes raises intracellular cyclic AMP and increases expression of tyrosinase and related enzymes. The downstream result is greater synthesis of eumelanin, the dark pigment, without ultraviolet exposure acting as the trigger. The compound is not selective, however, and also engages MC3R, MC4R and MC5R, which are expressed in the central nervous system and elsewhere. That lack of selectivity is the explanation usually offered for effects reported outside pigmentation, including appetite suppression and nausea. Selectivity remains a central theme in comparative studies of related peptides.
Human data remain limited and mostly short-term. Reports describe small trials and observational accounts rather than large controlled studies, so questions about dose-response relationships and long-term effects on melanocytes stay open. Whether repeated exposure alters naevus behaviour is not settled in the published record. Researchers also note that self-administered use outside clinical settings makes actual exposure difficult to quantify. Statements about efficacy and safety should therefore be read as preliminary rather than established.
| Property | Value | Notes |
|---|---|---|
| Compound class | Synthetic cyclic heptapeptide | Alpha-MSH analogue containing a D-phenylalanine residue |
| Molecular formula | C50H69N15O9 | Average molecular mass approximately 1024.2 g/mol |
| Appearance | White to off-white lyophilised powder | Normally supplied as a freeze-dried solid in a sealed vial |
| Solubility | Freely soluble in water and polar solvents | Dissolves readily in aqueous buffers and in alcohol-water mixtures |
| Receptor targets | MC1R, MC3R, MC4R, MC5R | Acts as a non-selective melanocortin receptor agonist |
Research interest has centred on photoprotection and pigmentation, with a smaller body of work on appetite and sexual function. Published human data remain limited to small, frequently uncontrolled studies, and the compound has never received marketing approval from a national medicines regulator. Most laboratory work treats it as a pharmacological tool for probing melanocortin signalling in cell culture or animal models. Whether pigmentation changes observed in people translate into measurable protection against ultraviolet-induced DNA damage remains an open question.
Melanotan-2 is a synthetic cyclic heptapeptide designed as an analogue of alpha-melanocyte-stimulating hormone, the naturally occurring peptide involved in pigmentation signalling. Its sequence is conventionally written as Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2, with a lactam bridge joining the aspartate side chain to the lysine side chain. The empirical formula is C50H69N15O9 and the monoisotopic mass lies near 1023.5 daltons. N-terminal acetylation and the D-configured phenylalanine both increase resistance to enzymatic breakdown compared with the parent hormone.
The peptide acts as a non-selective agonist at melanocortin receptors, showing affinity for MC1R, MC3R, MC4R and MC5R. Activation of MC1R on melanocytes drives the conversion of tyrosine into melanin and shifts production toward the darker eumelanin form. MC4R signalling in the central nervous system is linked to appetite and energy balance, which helps explain why reduced food intake appeared in early human studies. Effects on MC4R and on vascular tone also account for the erectile responses recorded as unexpected findings in those same trials.
Melanotan-2 is frequently confused with afamelanotide, a linear analogue authorised in the European Union for erythropoietic protoporphyria. The two compounds differ in chain length, ring structure and receptor selectivity, so findings for one cannot be transferred directly to the other. Published controlled human data on melanotan-2 remain sparse, and much of what circulates online derives from small studies or unpublished reports. Questions about effect size, dose-response behaviour and long-term safety therefore remain unresolved.
Melanotan II is a synthetic peptide analog modeled on alpha-melanocyte-stimulating hormone, a naturally occurring signaling peptide involved in pigmentation. Its structure is a cyclic heptapeptide containing two non-natural substitutions, norleucine at position four and D-phenylalanine at position seven. These modifications resist enzymatic breakdown and extend the molecule's activity relative to the native hormone. The compound binds melanocortin receptors and is studied mainly as a pharmacological tool rather than a therapeutic product. It has never received approval as a medicine in any major jurisdiction.
The compound was developed in the late 1980s and 1990s by academic researchers investigating photoprotection. The rationale held that stimulating melanin production might reduce ultraviolet damage to skin and lower skin cancer risk. Early work examined receptor binding, pigment response, and short-term tolerability in small studies. That program did not produce an approved drug, and formal development stalled after early-phase trials. Whether induced pigmentation confers meaningful photoprotection remains an open question.
Melanotan-2 is a synthetic cyclic heptapeptide designed as an analogue of alpha-melanocyte-stimulating hormone, a naturally occurring peptide involved in pigmentation signalling. Its sequence incorporates modified residues that increase potency and extend biological activity relative to the native hormone. The compound binds receptors of the melanocortin family and is examined mainly in laboratory research. It does not occur naturally and exists only as a manufactured chemical entity produced by solid-phase synthesis.
The peptide was developed during the 1980s by researchers investigating melanocortin signalling and skin pigmentation pathways. Early work focused on analogues of alpha-melanocyte-stimulating hormone that would resist enzymatic breakdown more effectively than the parent molecule. Melanotan-2 emerged from that programme as a shortened, cyclised variant. Reports describing its synthesis and receptor activity later appeared in the scientific literature. Commercial availability grew through unregulated channels rather than through pharmaceutical approval.
Structurally, Melanotan-2 retains the core recognition motif of alpha-melanocyte-stimulating hormone while adding a lactam bridge that links two side chains and constrains the molecule into a ring. This modification lowers susceptibility to enzymatic degradation. The compound acts as an agonist at melanocortin receptors, particularly subtypes associated with melanin production. Because the same receptor family influences several physiological processes, researchers note that its activity is not confined to pigmentation alone. Receptor selectivity continues to be examined in published studies.
During this period, royalist forces made advances into New Granada, which they controlled from 1815 to 1819, and into Chile, which they controlled from 1814 to 1817. Except for royalist areas in the northeast and south, the provinces of New Granada had maintained independence from Spain since 1810, unlike neighboring Venezuela, where royalists and pro-independence forces had exchanged control of the region several times. To pacify Venezuela and to retake New Granada, Spain organized in 1815 the largest armed force it ever sent to the New World, consisting of 10,500 troops and nearly sixty ships. Although this force was crucial in retaking a solidly pro-independence region like New Granada (see Spanish reconquest of New Granada), its soldiers were eventually spread out throughout Venezuela, New Granada, Quito, and Peru, and were lost to tropical diseases, diluting their impact on the war. More importantly, the majority of the royalist forces were composed, not of soldiers sent from the peninsula, but of Spanish Americans. Overall, Europeans formed only about a tenth of the royalist armies in Spanish America, and only about half of the expeditionary units, once they were deployed in the Americas. Since each European soldier casualty was replaced by a Spanish American soldier, over time, there were more and more Spanish American soldiers in the expeditionary units.
In 1884 German chemist Eugen Baumann found that reduction of cystine with zinc gave monomer, which he named "cysteïne". The easy redox interconversion of cysteine and cystine has "provided more puzzles to protein chemists than any of the other amino acids".
=== Parasitic disease === Ivermectin has been researched in laboratory animals, as a potential treatment for trichinosis and trypanosomiasis. Ivermectin has also been tested on zebrafish infected with Pseudocapillaria tomentosa.
primary reconstruction: the replacement of breast tissues damaged by trauma (blunt, penetrating, blast), disease (breast cancer), and failed anatomic development (tuberous breast deformity). revision and reconstruction: to revise (correct) the outcome of a previous breast reconstruction surgery. primary augmentation: to aesthetically augment the size, form, and feel of the breasts. The operating room time of post–mastectomy breast reconstruction, and of breast augmentation surgery is determined by the procedure employed, the type of incisions, the breast implant (type and materials), and the pectoral locale of the implant pocket. Recent research has indicated that mammograms should not be done with any greater frequency than that used in normal procedure in patients undergoing breast surgery, including breast implant, augmentation, mastopexy, and breast reduction.
Sources: en.wikipedia.org
==== August 2015 Salmonella ==== At almost the same time as the Simi Valley norovirus outbreak, Minnesota health officials confirmed a Salmonella outbreak that affected 17 Minneapolis-area Chipotle restaurants in mid-August 2015. The source of the outbreak was traced back to contaminated tomatoes that were grown in Mexico. The Minnesota Department of Health reported that samples from 45 victims were tested and found that their illness was caused by the Salmonella Newport bacterium as determined by DNA profiling. Later, the state officials reported that the total of persons who became infected was increased to 64 and the number Chipotle locations in which they had acquired the bacterium was increased to 22, all located within the state of Minnesota.
== Chemistry == 2C-B, also known as 4-bromo-2,5-dimethoxyphenethylamine, is a substituted phenethylamine of the 2C family, also known as the 4-substituted 2,5-dimethoxyphenethylamines. It is a synthetic analogue of the naturally occurring phenethylamine psychedelic mescaline found in peyote and certain other cacti.
However, the amount of radium produced globally has always been small in comparison to other elements, and by the 2010s, annual production of radium, mainly via extraction from spent nuclear fuel, was less than 100 grams. In nature, radium is found in uranium ores in quantities as small as a seventh of a gram per ton of uraninite, and in thorium ores in trace amounts. Radium is not necessary for living organisms, and its radioactivity and chemical reactivity make adverse health effects likely when it is incorporated into biochemical processes because of its chemical mimicry of calcium, due to them both being group 2 elements. As of 2018, other than in nuclear medicine, radium has no commercial applications. Formerly, from the 1910s to the 1970s, it was used as a radioactive source for radioluminescent devices and also in radioactive quackery for its supposed curative power. In nearly all of its applications, radium has been replaced with less dangerous radioisotopes, with one of its few remaining non-medical uses being the production of actinium in nuclear reactors.
Methylphenidate is a psychostimulant drug that is often used in the treatment of ADHD and narcolepsy and occasionally to treat obesity in combination with diet restraints and exercise. Its effects at therapeutic doses include increased focus, increased alertness, decreased appetite, decreased need for sleep and decreased impulsivity. Methylphenidate is not usually used recreationally, but when it is used, its effects are similar to those of amphetamines. Methylphenidate acts as a norepinephrine–dopamine reuptake inhibitor (NDRI), by blocking the norepinephrine transporter (NET) and the dopamine transporter (DAT). Methylphenidate has a higher affinity for the dopamine transporter than for the norepinephrine transporter, and so its effects are mainly due to elevated dopamine levels caused by the inhibited reuptake of dopamine, however increased norepinephrine levels also contribute to various of the effects caused by the drug. Methylphenidate is sold under a number of brand names including Ritalin. Other versions include the long lasting tablet Concerta and the long lasting transdermal patch Daytrana.
Anshel Pfeffer(Hebrew: אנשיל פפר, born 22 June 1973); British -Israeli journalist; a senior correspondent and columnist for Haaretz, covering military, Jewish and international affairs, and Israel correspondent for The Economist.; has also written for The Guardian, The New York Times, The Washington Post and The Times; received the B'nai B'rith award for "Recognizing Excellence in Diaspora Reportage" Melanie Phillips,(born 4 June 1951) Neoconservative, and right wing hawkish pro Zionist journalist; began her career writing for The Guardian and New Statesman; during the 1990s, she came to identify with ideas more associated with the right and currently writes for The Times, The Jerusalem Post, and The Jewish Chronicle, covering political and social issues from a social conservative perspective.Irving Kristol, defines her as a liberal who has "been mugged by reality";was panellist on BBC Radio 4 programme The Moral Maze and BBC One's Question Time; was awarded the Orwell Prize for Journalism Hella Pick CBE (24 April 1929 – 4 April 2024); in 1960, was UN correspondent of The Guardian newspaper, tutored by chief US correspondent Alistair Cooke; awarded CBE in 2000; was Arts & Culture Programme Director at Institute for Strategic Dialogue, an independent think-tank based in London; author ofSimon Wiesenthal: A Life in Search of Justice, Weidenfeld & Nicolson, 1996; Guilty Victim – Austria from the Holocaust to Haider, I B Tauris & Co Ltd, 2000 and Invisible Walls, Weidenfeld & Nicolson, 2021 Gabriel Pogrund (born 1993 or 1994) is a journalist who has worked for the New Statesman, Shortlist, Ha'aretz and Jewish News and is currently Whitehall editor at The Sunday Times; won 2017 Young Journalist of the Year at the British Press Awards and in 2018 was a Stern Fellow at The Washington Post. In 2020 Pogrund and Patrick Maguire published Left Out: The Inside Story of Labour Under Corbyn, which in part, addresses charges of, and assumptions about 'the new anti-Semitism' in the Labour Party. Eve Pollard Evelyn, Lady Lloyd, (née Pollard, formerly Winkleman, born 25 December 1943); has been the editor of several tabloid newspapers; was fashion editor at Honey magazine; also worked for Daily Mirror; was launch editor-in-chief of Elle magazine in the US and edited Sunday magazine for the News of the World and You magazine for the Mail on Sunday; also worked in television as features editor of TV-am (1982–1983) and devised Frocks on the Box for ITV contractor TVS.; often appeared on radio and TV; was regular participant in Through the Keyhole; was a guest panellist on the talk show Loose Women; in 2016, was appointed the first Chair of Reporters without Borders in the UK. In June 2019, was awarded the prestigious Journalist Laureate prize by the London Press Club. 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He is also Chairman of the MOBO Charity Foundation (Music of Black Origin), a Trustee of both ChickenShed (Theatre Changing Lives), Patron of the Royal Television Society and co-chairman of the Classic BRITS, and a supporter of Norwood. He gave evidence to Leveson Inquiry into practices and ethics of British Press and was awarded the OBE in 2014 for services to entertainment industry. He also holds an honorary professorship, awarded in 2012, and honorary doctorate at Henley Business School of Reading University in recognition of his contribution to the arts, music and broadcasting. Miriam Shaviv (born 24 August 1976), columnist for "The Jewish Chronicle", "Haaretz", "The Times of Israel", "The Forward"; former literary editor of The Jerusalem Post; Features Editor of the "Times Higher Education" magazine. David Shukman (born 30 May 1958) journalist, and the former science editor of BBC News. 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In 2019 he represented Campaign Against Antisemitism (CAA) in its case a formal investigation under section 20 of the Equality Act 2006 into whether Labour Party had "unlawfully discriminated against, harassed or victimised people because they are Jewish"; specialist in human rights and public law, including COVID-19 lockdown rules. George Weidenfeld, Baron Weidenfeld, (13 September 1919 – 20 January 2016) was a British publisher, philanthropist, and newspaper columnist. He was also a lifelong Zionist and renowned as a master networker. He was on good terms with popes, prime ministers and presidents and put his connections to good use for diplomatic and philanthropic ends; founder of Institute for Strategic Dialogue Victor Weisz, Vicky, cartoonist Claudia Winkleman (born 15 January 1972); television presenter, radio personality, film critic and journalist; has written for The Sunday Times, The Independent, London paper Metro and has written opinion-led lifestyle journalism for Cosmopolitan, Tatler and The Independent; has also written for BBC, Daily Mail, The Mirror UK, The Sun, The Telegraph, Daily Express, The Times, and Radio Times Jonathan Wittenberg (born 17 September 1957 in Glasgow, Scotland); Masorti rabbi, the Senior Rabbi of Masorti Judaism UK; leading writer and thinker on Judaism; has written for The Guardian, Daily Mirror, HuffPost, Times of Israel, Haaretz, and The Jewish Chronicle. He is Rabbi of the New North London Synagogue,; member of the Elijah Interfaith Institute Board of World Religious Leaders.; has featured on Thought for the Day on the BBC Radio Four Today programme. Martin Wolf (born 16 August 1946 in London) journalist; chief economics commentator at the Financial Times; widely regarded as one of the most influential economics journalists in the world. Lawrence H. Summers called him "the world's preeminent financial journalist." Mohamed A. El-Erian, former CEO of the PIMCO, said Wolf is "by far, the most influential economic columnist out there".Prospect magazine described him as "the Anglosphere's most influential finance journalist",; Kenneth Rogoff said, "He really is the premier financial and economics writer in the world". In 2012, he received the Ischia International Journalism Award.In 2019, Wolf received the Gerald Loeb Lifetime Achievement Award from the UCLA Anderson School of Management. Donald Zec (12 March 1919 – 6 September 2021); author of over ten books, newspaper journalist and biographer; worked for the Daily Mirror for 40 years.
Sources: en.wikipedia.org
No. It is a laboratory-made peptide, while the natural hormone is alpha-melanocyte-stimulating hormone, a longer peptide produced by the pituitary gland and by skin cells. Melanotan-2 mimics only a short active region of that hormone and contains non-natural residues such as D-phenylalanine.
No approved regulatory indication exists in major markets. An approval exists for a different peptide, afamelanotide, which is used for a rare photosensitivity disorder called erythropoietic protoporphyria. Melanotan-2 itself remains a research compound with no cleared clinical role.
Melanocortin-1 receptors on melanocytes are the receptor most closely linked to pigment production. The peptide is not selective, however, and also activates melanocortin-3, melanocortin-4, and melanocortin-5 receptors. That lack of selectivity is the usual explanation offered for both its range of observed effects and its off-target effects.
It is a synthetic cyclic heptapeptide and a non-selective melanocortin receptor agonist. Structurally it is modelled on alpha-melanocyte-stimulating hormone, a peptide that occurs naturally in the body.