References
Sources, in one place
Every source cited on a published page, together with the standing regulators, registries and reporting standards this site points readers towards. Sources attached to unpublished records do not appear here.
Showing all 233 references.
- Reporting standard
US National Library of Medicine · accessed 20 August 2026
Confirms this is a small molecule rather than a peptide.
Cited in: 5-amino-1MQ
- Primary researchCitation not yet verified
Acta Paediatrica Supplement, 1993 · doi:10.1111/j.1651-2227.1993.tb12834.x (opens doi.org in a new tab)
Found growth hormone clearly superior. Bibliographic record confirmed via Europe PMC.
Cited in: Sermorelin
- Primary research
Medvedev VE, Tereshchenko ON, Israelian AIu, et al.. Zhurnal Nevrologii i Psikhiatrii im. S.S. Korsakova, 2014
Russian language. Active comparator, no placebo arm.
Cited in: Selank
- Primary researchCitation not yet verified
Lois N, et al.. Journal of Clinical Medicine, 2020 · doi:10.3390/jcm9072225 (opens doi.org in a new tab)
Negative on every objective endpoint. DOI confirmed registered via Crossref; the publisher page blocks automated access.
Cited in: ARA-290
- Primary research
Genetics in Medicine, 2021 · doi:10.1038/s41436-020-01006-8 (opens doi.org in a new tab)
Neither primary endpoint was met in the randomised phase.
Cited in: SS-31
- Primary researchCitation not yet verified
Grant R, Berg J, Mestayer R, et al.. Frontiers in Aging Neuroscience, 2019 · doi:10.3389/fnagi.2019.00257 (opens doi.org in a new tab)
The only human pharmacokinetic data for the infused form. Bibliographic record confirmed via Europe PMC.
Cited in: NAD+
- Primary research
Van Den Neste E, et al.. Cancer Chemotherapy and Pharmacology, 2013 · doi:10.1007/s00280-012-2033-5 (opens doi.org in a new tab)
Cited in: AICAR
- Regulator or official body
electronic Medicines Compendium · accessed 20 August 2026
Across 163 active ingredients beginning with A the index carries no entry for acadesine. No UK marketing authorisation exists, and none was established in any jurisdiction; development was discontinued after the phase 3 failure.
Cited in: AICAR
- Regulator or official body
electronic Medicines Compendium · accessed 20 August 2026
Across seventy active ingredients beginning with N the index lists nicotinamide but no entry for nicotinamide adenine dinucleotide. No NAD+ injectable holds a UK marketing authorisation, and none was found in any other jurisdiction. Of the oral precursors, nicotinamide riboside chloride is an authorised novel food in Great Britain; nicotinamide mononucleotide is not authorised and remains under assessment.
Cited in: NAD+
- Primary researchCitation not yet verified
Schneider-Helmert D, Gnirss F, Monnier M, et al.. International Journal of Clinical Pharmacology, Therapy and Toxicology, 1981
Six normal volunteers. Bibliographic record confirmed via Europe PMC.
Cited in: DSIP
- Primary research
von Walden F, Fernandez-Gonzalo R, Norrbom J, et al.. Journal of Applied Physiology, 2021
Cited in: MOTS-c
- GuidanceCitation not yet verified
Advertising Standards Authority (opens asa.org.uk in a new tab)
ASA · accessed 17 August 2026
- Regulator or official body
Afamelanotide 16mg implant (Scenesse) — SMC advice (opens scottishmedicines.org.uk in a new tab)
Scottish Medicines Consortium, 2021 · accessed 20 August 2026
Records the licensed indication — prevention of phototoxic reactions in patients with erythropoietic protoporphyria — and that the product was authorised under exceptional circumstances in November 2014. The SMC accepted it for use in NHS Scotland. Afamelanotide is prescription only and restricted to specialist prescribers.
Cited in: Melanotan I
- Review or secondary sourceCitation not yet verified
Višnjić D, et al.. Cells, 2021 · doi:10.3390/cells10051095 (opens doi.org in a new tab)
DOI confirmed registered via Crossref; the publisher page blocks automated access.
Cited in: AICAR
- Reporting standard
Ala-Glu-Asp-Pro, PubChem compound record CID 18439621 (opens pubchem.ncbi.nlm.nih.gov in a new tab)
US National Library of Medicine · accessed 20 August 2026
Confirms the tetrapeptide sequence and lists Cortagen among its synonyms.
Cited in: Cortagen
- Review or secondary source
Böhm M, et al.. Journal of the European Academy of Dermatology and Venereology, 2025 · doi:10.1111/jdv.20269 (opens doi.org in a new tab)
Cited in: Melanotan II
- Regulator or official body
legislation.gov.uk, 2001 · accessed 22 August 2026
Lists “Botulinum toxins” under TOXINS. Premises holding listed toxins are subject to notification and security requirements under Part 7 of the Act.
Cited in: Botulinum toxin
- Primary research
Dahan A, et al.. Molecular Medicine, 2013 · doi:10.2119/molmed.2013.00122 (opens doi.org in a new tab)
Cited in: ARA-290
- Reporting standardCitation not yet verified
ARRIVE guidelines for reporting animal research (opens arriveguidelines.org in a new tab)
NC3Rs · accessed 17 August 2026
Cited to show how a reporting standard is presented alongside primary findings.
Cited in: Illustrative Compound BETA-2
- Regulator or official body
Scottish Medicines Consortium, 2017 · accessed 22 August 2026
Advice of 11 December 2017 on the licensed UK product: aviptadil 25 micrograms with phentolamine mesilate 2 mg, intracavernosal injection, prescription-only. Confirms the licensed indication in erectile dysfunction.
Cited in: VIP
- Regulator or official body
electronic Medicines Compendium, 2012 · accessed 20 August 2026
PL 00057/0934, Pfizer Limited, first authorised 29 March 2012. Legal category: Prescription only medicine. The authorised indication is narrow — it is licensed as the diluent syringe for one named product, not as a general-purpose diluent.
Cited in: Bacteriostatic water
- Primary researchCitation not yet verified
Popovic V, Damjanovic S, Micic D, et al.. Journal of Clinical Endocrinology and Metabolism, 1995 · doi:10.1210/jcem.80.3.7883854 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: GHRP-6
- Regulator or official body
electronic Medicines Compendium, 2024 · accessed 22 August 2026
Botulinum toxin type A, AbbVie Ltd. Legal category: prescription-only medicine. Licensed indications span focal spasticity, cervical dystonia, chronic migraine, overactive bladder, severe hyperhidrosis and defined aesthetic uses.
Cited in: Botulinum toxin
- Review or secondary source
Rossetto O, Pirazzini M, Montecucco C. Nature Reviews Microbiology, 2014
Cited in: Botulinum toxin
- Review or secondary source
Herd CP, et al.. Cochrane Database of Systematic Reviews, 2018
Cited in: Botulinum toxin
- Primary research
Sudarkina OY, Filippenkov IB, Stavchansky VV, et al.. International Journal of Molecular Sciences, 2021
Cited in: Semax
- Primary research
Kingsberg SA, Clayton AH, Portman D, et al.. Obstetrics and Gynecology, 2019 · doi:10.1097/AOG.0000000000003500 (opens doi.org in a new tab)
Cited in: PT-141
- Review or secondary source
Edinoff AN, et al.. Neurology International, 2022 · doi:10.3390/neurolint14010006 (opens doi.org in a new tab)
Records the modest effect sizes and the non-significant secondary endpoint.
Cited in: PT-141
- GuidanceCitation not yet verified
British Pharmacopoeia (opens pharmacopoeia.com in a new tab)
British Pharmacopoeia Commission · accessed 17 August 2026
Publishes general methods and monograph requirements used as reference points for analytical practice in the UK.
Cited in: What peptide purity percentages do and do not mean, Identity testing, High-performance liquid chromatography, Microbiological testing, Endotoxin testing
- Primary research
Carvas AO et al.. eBioMedicine, 2025 · doi:10.1016/j.ebiom.2025.105836 (opens doi.org in a new tab)
Cited in: Cagrilintide
- Primary researchCitation not yet verified
Buse JB, Bajaj HS, Dalskov SM, et al.. The Lancet Diabetes & Endocrinology, 2026 · doi:10.1016/s2213-8587(26)00125-7 (opens doi.org in a new tab)
The trial that compares the combination against each constituent separately. Bibliographic record confirmed via Europe PMC.
Cited in: Cagrilintide and semaglutide combination
- Primary researchCitation not yet verified
Cardiac effects of hexarelin in hypopituitary adults (opens doi.org in a new tab)
Bisi G, Podio V, Valetto MR, et al.. European Journal of Pharmacology, 1999 · doi:10.1016/s0014-2999(99)00537-3 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: Hexarelin
- Review or secondary source
Carnitine transport and fatty acid oxidation (opens pubmed.ncbi.nlm.nih.gov in a new tab)
Longo N, Frigeni M, Pasquali M. Biochimica et Biophysica Acta, 2016
Cited in: L-Carnitine
- Primary research
Muresanu DF, Heiss WD, Hoemberg V, et al.. Stroke, 2016 · doi:10.1161/STROKEAHA.115.009416 (opens doi.org in a new tab)
Reported large superiority on upper-limb function. Funded by the manufacturer, with multiple authors declaring grants, consultancy or employment with it.
Cited in: Cerebrolysin
- Review or secondary source
Cerebrolysin for acute ischaemic stroke (opens cochrane.org in a new tab)
Ziganshina LE, Abakumova T, Nurkhametova D, et al.. Cochrane Database of Systematic Reviews, 2023 · doi:10.1002/14651858.CD007026.pub7 (opens doi.org in a new tab)
Seven trials, 1,773 participants. Note that this review pooled in a bovine-derived comparator, so its conclusion mentions cattle brain; Cerebrolysin itself is porcine.
Cited in: Cerebrolysin
- Review or secondary source
Cerebrolysin for vascular dementia (opens cochrane.org in a new tab)
Cui S, Chen N, Yang M, et al.. Cochrane Database of Systematic Reviews, 2019 · doi:10.1002/14651858.CD008900.pub3 (opens doi.org in a new tab)
Six trials, 597 participants. Graded very low quality; the authors conclude the data are not definitive and effects may be too small to be clinically meaningful.
Cited in: Cerebrolysin
- Primary researchCitation not yet verified
Martens CR, Denman BA, Mazzo MR, et al.. Nature Communications, 2018 · doi:10.1038/s41467-018-03421-7 (opens doi.org in a new tab)
Concerns an oral precursor, not NAD+ itself. Bibliographic record confirmed via Europe PMC.
Cited in: NAD+
- Regulator or official body
Cibinetide — orphan designation EU/3/13/1191 (opens ema.europa.eu in a new tab)
European Medicines Agency, 2013 · accessed 20 August 2026
The page states plainly that an orphan designation is not a marketing authorisation. This is also an EU designation rather than a Great Britain one, so it confers no GB status. No UK marketing authorisation exists — confirmed against the electronic Medicines Compendium ingredient index, which lists 201 active ingredients beginning with C and carries no entry for cibinetide.
Cited in: ARA-290
- Primary research
Culver DA, et al.. Investigative Ophthalmology and Visual Science, 2017 · doi:10.1167/iovs.16-21291 (opens doi.org in a new tab)
Primary endpoint significant in only one of three dose groups; the pain difference was not significant.
Cited in: ARA-290
- Trial registryCitation not yet verified
ClinicalTrials.gov (opens clinicaltrials.gov in a new tab)
National Library of Medicine · accessed 17 August 2026
Cited in: Illustrative Compound ALPHA-1, Research evidence versus clinical evidence
- Review or secondary sourceCitation not yet verified
Cochrane Library (opens cochranelibrary.com in a new tab)
Cochrane · accessed 17 August 2026
- Primary researchCitation not yet verified
Sampson CM, et al.. Scientific Reports, 2021 · doi:10.1038/s41598-021-85051-6 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: 5-amino-1MQ
- Regulator or official body
legislation.gov.uk, 2019 · accessed 20 August 2026
The glossary contains Copper Tripeptide-1 and Copper Tripeptide-34, but no entry for Copper Tripeptide-3 — the name suppliers commonly attach to this compound. So unlike some related peptides it has no verified Great Britain cosmetic-ingredient identity. In any case the cosmetics regime reaches only the external parts of the body, so an injectable presentation falls outside it entirely and no UK marketing authorisation exists.
- Review or secondary sourceCitation not yet verified
Antiviral Research, 2008 · doi:10.1016/j.antiviral.2007.10.014 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not directly accessible.
Cited in: Thymosin alpha-1
- Review or secondary source
Cosmeceutical Peptides in the Framework of Sustainable Wellness Economy (opens doi.org in a new tab)
Errante F, et al.. Frontiers in Chemistry, 2020 · doi:10.3389/fchem.2020.572923 (opens doi.org in a new tab)
Attributes the circulating mechanistic figure to manufacturer material rather than to a published experiment.
Cited in: SNAP-8
- Review or secondary sourceCitation not yet verified
Delta sleep-inducing peptide (DSIP): a still unresolved riddle (opens doi.org in a new tab)
Kovalzon VM, Strekalova TV. Journal of Neurochemistry, 2006 · doi:10.1111/j.1471-4159.2006.03693.x (opens doi.org in a new tab)
States that the link between this peptide and sleep has never been further characterised, in part because of the lack of isolation of its gene, protein and possible receptor. Bibliographic record confirmed via Europe PMC.
Cited in: DSIP
- Regulator or official body
US Food and Drug Administration, Federal Register, 2013 · accessed 20 August 2026
Correcting a common claim: the historical licence was a United States one, discontinued by the manufacturer in 2008. No current UK marketing authorisation exists, and whether a separate UK or EU authorisation ever existed could not be established.
Cited in: Sermorelin
- Primary researchCitation not yet verified
Petersenn S, Jung R, Beil FU. European Journal of Endocrinology, 2002 · doi:10.1530/eje.0.1460667 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page returned an access error.
Cited in: GHRP-6
- Primary researchCitation not yet verified
Yang SY, Goldspink G. FEBS Letters, 2002 · doi:10.1016/S0014-5793(02)02918-6 (opens doi.org in a new tab)
The original finding. Bibliographic record confirmed via Europe PMC.
Cited in: MGF
- Primary researchCitation not yet verified
Human Reproduction, 2015 · doi:10.1093/humrep/dev143 (opens doi.org in a new tab)
Registration confirmed via the Crossref API; the publisher page blocks automated access.
Cited in: Kisspeptin-10
- Primary research
Lau J, et al.. Journal of Medicinal Chemistry, 2015
Cited in: Semaglutide
- Trial registry
ClinicalTrials.gov · accessed 19 August 2026
Phase 2, 72 participants, completed with results posted. Used full-length thymosin beta-4, not the fragment.
Cited in: TB-500
- Primary researchCitation not yet verified
Larsen AT et al.. Biomedicine & Pharmacotherapy, 2022 · doi:10.1016/j.biopha.2022.113842 (opens doi.org in a new tab)
Bibliographic record confirmed via the NCBI E-utilities API; the publisher page was not directly accessible.
Cited in: Cagrilintide
- Regulator or official body
EarCalm Spray — Summary of Product Characteristics (opens medicines.org.uk in a new tab)
electronic Medicines Compendium, 2008 · accessed 20 August 2026
PL 14017/0310. Glacial acetic acid 2.0 per cent weight for weight, for superficial infections of the external ear canal. Legal category: Pharmacy. This is the only UK product with acetic acid as an active ingredient outside two combination ear preparations. There is no UK-authorised acetic acid injection or injectable diluent.
Cited in: Acetic acid solution
- Primary researchCitation not yet verified
Newman MF, et al.. JAMA, 2012 · doi:10.1001/jama.2012.7633 (opens doi.org in a new tab)
Stopped early for futility. DOI confirmed registered via Crossref with matching title; the publisher page blocks automated access.
Cited in: AICAR
- Primary research
Anisimov VN, Khavinson VKh, Popovich IG, et al.. Biogerontology, 2003
Found no effect on mean lifespan.
Cited in: Epitalon
- Primary research
Stanley TL, et al.. JAMA, 2014
Cited in: Tesamorelin
- Primary researchCitation not yet verified
Effect of tetrapeptide cortagen on regeneration of sciatic nerve (opens doi.org in a new tab)
Turchaninova LN, Kolosova LI, Malinin VV, et al.. Bulletin of Experimental Biology and Medicine, 2000 · doi:10.1023/a:1017532001908 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Cortagen
- Primary research
Gusev EI, Skvortsova VI, Miasoedov NF, et al.. Zhurnal Nevrologii i Psikhiatrii im. S.S. Korsakova, 1997
Russian language. Non-randomised allocation, with an unmatched control group.
Cited in: Semax
- Primary research
Biçer O, Adanir O, Güleryüz Y, et al.. Joint Diseases and Related Surgery, 2026 · doi:10.52312/jdrs.2026.2951 (opens doi.org in a new tab)
The only published study testing any of these marketed blends against its own constituents. The combination showed no additive benefit and did not reach significance on the biomechanical endpoint that the single agent did.
Cited in: BPC-157 and TB-500 combination
- Primary researchCitation not yet verified
Bes F, Hofman W, Schuur J, et al.. Neuropsychobiology, 1992 · doi:10.1159/000118919 (opens doi.org in a new tab)
Sixteen patients. Concluded short-term treatment is not likely to be of major therapeutic benefit. Bibliographic record confirmed via Europe PMC.
Cited in: DSIP
- Primary researchCitation not yet verified
Effects of short peptides on lymphocyte chromatin in senile subjects (opens doi.org in a new tab)
Khavinson VKh, Lezhava TA, Malinin VV. Bulletin of Experimental Biology and Medicine, 2004 · doi:10.1023/b:bebm.0000024393.40560.05 (opens doi.org in a new tab)
Cell culture using human donor lymphocytes. Not a clinical study, despite frequently being cited as one. Bibliographic record confirmed via Europe PMC.
Cited in: Cortagen
- Primary research
Miller TR, Wagner JD, Baack BR, et al.. Archives of Facial Plastic Surgery, 2006
Thirteen completers. No significant difference on objective endpoints.
Cited in: GHK-Cu
- Primary research
Zozulya AA, Neznamov GG, Siuniakov TS, et al.. Zhurnal Nevrologii i Psikhiatrii im. S.S. Korsakova, 2008
Russian language. Active comparator, no placebo arm.
Cited in: Selank
- Primary researchCitation not yet verified
Yamauchi T, Becker NP, Hagemann CA, et al.. The Lancet Diabetes & Endocrinology, 2026 · doi:10.1016/s2213-8587(25)00402-4 (opens doi.org in a new tab)
Bibliographic record and abstract confirmed via the Europe PMC API; the publisher page was not opened, so this is marked unverified.
Cited in: Cagrilintide and semaglutide combination
- Primary research
Neurology, 2023 · doi:10.1212/WNL.0000000000207402 (opens doi.org in a new tab)
Missed both co-primary endpoints.
Cited in: SS-31
- Primary research
Avcil M, et al.. Journal of Cosmetic Dermatology, 2020 · doi:10.1111/jocd.13009 (opens doi.org in a new tab)
Uncontrolled, and tested five actives together.
Cited in: SNAP-8
- Primary researchCitation not yet verified
Venkova K, Fraser G, Hoveyda HR, et al.. Journal of Pharmacology and Experimental Therapeutics, 2009 · doi:10.1124/jpet.108.149211 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Ipamorelin
- Regulator or official body
European Medicines Agency, 2012 · accessed 22 August 2026
Application withdrawn 21 June 2012 after the CHMP provisionally concluded that benefits did not outweigh risks.
Cited in: Tesamorelin
- Regulator or official body
NIHR Innovation Observatory, 2024 · accessed 20 August 2026
States that elamipretide does not hold a marketing authorisation in the EU or UK for any indication. Corroborated by its absence from the electronic Medicines Compendium ingredient index. A US accelerated approval was granted in September 2025 for Barth syndrome; that confers no UK status, and a UK paediatric investigation plan is a development-stage agreement rather than an authorisation.
Cited in: SS-31
- Primary researchCitation not yet verified
Circulation, 2023 · doi:10.1161/CIRCULATIONAHA.122.058794 (opens doi.org in a new tab)
The key contrary finding. Bibliographic record confirmed via Europe PMC and the DOI verified as registered via Crossref.
Cited in: FOXO4-DRI
- Review or secondary source
Vasireddi N, Hahamyan H, Salata MJ, et al.. HSS Journal, 2025 · doi:10.1177/15563316251355551 (opens doi.org in a new tab)
Cited in: BPC-157
- Primary research
Khavinson VKh, Bondarev IE, Butyugov AA. Bulletin of Experimental Biology and Medicine, 2003
Cited in: Epitalon
- Reporting standardCitation not yet verified
EQUATOR Network reporting guidelines (opens equator-network.org in a new tab)
EQUATOR Network · accessed 17 August 2026
Index of CONSORT, STROBE, ARRIVE and related reporting standards referred to in this article.
- Primary research
Europe PMC REST API, 2026 · accessed 20 August 2026
Cited as the evidence for a negative. The query returns hitCount 0. A companion search for "adamax AND peptide" returned 18 records, none of them about this compound — all were unrelated computational and machine-learning papers. Re-running this URL reproduces the result.
Cited in: Adamax
- Primary research
Mahlapuu M, Sidorowicz A, Mikosinski J, et al.. Wound Repair and Regeneration, 2021 · doi:10.1111/wrr.12977 (opens doi.org in a new tab)
Failed its primary endpoint.
Cited in: LL-37
- Review or secondary source
Adnan SB, Maarof M, Fauzi MB, et al.. International Journal of Medical Sciences, 2025
States that clinical trial data for this compound are lacking.
Cited in: GHK-Cu
- Review or secondary source
Adnan SB, Maarof M, Fauzi MB, et al.. International Journal of Medical Sciences, 2025 · doi:10.7150/ijms.118118 (opens doi.org in a new tab)
Cited in: Klow combination
- Primary research
Shehab N, et al.. Pediatric Critical Care Medicine, 2009 · doi:10.1097/PCC.0b013e31819a383c (opens doi.org in a new tab)
Cited in: Bacteriostatic water
- Primary researchCitation not yet verified
Hameed M, et al.. Journal of Physiology, 2003 · doi:10.1113/jphysiol.2002.032136 (opens doi.org in a new tab)
Measured endogenous expression; the peptide was not administered. Bibliographic record confirmed via NCBI E-utilities.
Cited in: MGF
- Regulator or official body
FDA Grants Accelerated Approval to First Treatment for Barth Syndrome (opens fda.gov in a new tab)
US Food and Drug Administration, 2025 · accessed 20 August 2026
United States only. Accelerated approval on an intermediate endpoint, with a confirmatory trial required.
Cited in: SS-31
- Primary research
Aging, 2020 · doi:10.18632/aging.102682 (opens doi.org in a new tab)
Independent group.
Cited in: FOXO4-DRI
- Regulator or official body
Medicines and Healthcare products Regulatory Agency, 2024 · accessed 20 August 2026
States that products containing this substance are classified as medicines if injectable, that the MHRA has repeatedly acted to remove such products from the market for over ten years, and that users should stop immediately. An earlier response frames classification less absolutely, noting it is decided case by case rather than automatically.
Cited in: Melanotan II
- Primary research
Filatova E, Kasian A, Kolomin T, et al.. Frontiers in Pharmacology, 2017
Cited in: Selank
- Primary research
Wang X, et al.. Wound Repair and Regeneration, 2017
Cited in: GHK-Cu
- Reporting standard
Glu-Asp-Arg, PubChem compound record CID 10273502 (opens pubchem.ncbi.nlm.nih.gov in a new tab)
US National Library of Medicine · accessed 20 August 2026
Confirms the tripeptide sequence and lists Pinealon among its synonyms.
Cited in: Pinealon
- Review or secondary source
Sonthalia S, Daulatabad D, Sarkar R. Indian Journal of Dermatology, Venereology and Leprology, 2016
Cited in: Glutathione
- Review or secondary source
Glutathione metabolism and its implications for health (opens pubmed.ncbi.nlm.nih.gov in a new tab)
Wu G, et al.. The Journal of Nutrition, 2004
Cited in: Glutathione
- Primary researchCitation not yet verified
Gajda M, et al.. Drug Testing and Analysis, 2019 · doi:10.1002/dta.2489 (opens doi.org in a new tab)
Forensic chemistry on seized material. Bibliographic record confirmed via Europe PMC.
Cited in: CJC-1295 with DAC, CJC-1295 without DAC
- Regulator or official body
electronic Medicines Compendium, 2021 · accessed 22 August 2026
PL 17509/0005. Legal category: prescription-only medicine. Licensed for evaluating the functional capacity and response of the gonadotropes of the anterior pituitary.
Cited in: Gonadorelin
- Regulator or official body
US Food and Drug Administration · accessed 20 August 2026
Searched directly and re-verified on alternative terms. No notice exists, therefore no FDA response letter exists. No UK marketing authorisation and no UK novel food authorisation either, so there is no lawful route to sale as a food or supplement in Great Britain.
Cited in: AOD-9604
- Primary research
Laferrère B, Abraham C, Russell CD, et al.. Journal of Clinical Endocrinology and Metabolism, 2005 · doi:10.1210/jc.2004-1719 (opens doi.org in a new tab)
Seven participants.
Cited in: GHRP-2
- Primary researchCitation not yet verified
Growth hormone status during long-term hexarelin therapy (opens doi.org in a new tab)
Rahim A, O’Neill PA, Shalet SM. Journal of Clinical Endocrinology and Metabolism, 1998 · doi:10.1210/jcem.83.5.4812 (opens doi.org in a new tab)
The sixteen-week study documenting the decline in response. Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: Hexarelin
- Review or secondary source
Svensson D, Nilsson BO. Inflammation Research, 2025 · doi:10.1007/s00011-025-02005-8 (opens doi.org in a new tab)
Cited in: LL-37
- Primary researchCitation not yet verified
Gombart AF, Borregaard N, Koeffler HP. FASEB Journal, 2005 · doi:10.1096/fj.04-3284com (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: LL-37
- Regulator or official bodyCitation not yet verified
Human Tissue Authority (opens hta.gov.uk in a new tab)
HTA · accessed 17 August 2026
Relevant where material is derived from human tissue or cells.
- Regulator or official body
electronic Medicines Compendium, 2026 · accessed 20 August 2026
PL 12762/0008, Mercury Pharmaceuticals Ltd. Legal category: Prescription only medicine. Cited to establish that injectable vitamin B12, a common constituent of these mixtures, is prescription only in the UK. Oral B12 is not — the distinction is the route, not the molecule.
Cited in: Lipo-C, Vitamin B12
- Primary researchCitation not yet verified
Proceedings of the National Academy of Sciences, 2003 · doi:10.1073/pnas.1834399100 (opens doi.org in a new tab)
Registration confirmed via the Crossref API; the publisher page blocks automated access.
Cited in: Kisspeptin-10
- Primary research
Belchetz PE, et al.. Science, 1978
The pulsatile-versus-continuous experiment on which the field turns.
Cited in: Gonadorelin
- GuidanceCitation not yet verified
ICH guidelines (opens ich.org in a new tab)
International Council for Harmonisation · accessed 17 August 2026
Includes Q2 on validation of analytical procedures, which underpins what a stated method can support.
Cited in: What a certificate of analysis actually shows, What peptide purity percentages do and do not mean, Identity testing, Purity analysis, High-performance liquid chromatography, Mass spectrometry, Interpreting certificates of analysis, Storage conditions, Stability testing
- Primary researchCitation not yet verified
White A, Stremming J, Wesolowski SR, et al.. American Journal of Physiology: Endocrinology and Metabolism, 2025 · doi:10.1152/ajpendo.00259.2024 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: IGF-1 LR3
- Regulator or official body
electronic Medicines Compendium · accessed 20 August 2026
Included for contrast. Mecasermin is recombinant human IGF-1 and IS a UK licensed medicine, marketing authorisation PL 08498/0041, for severe primary IGF-1 deficiency in children. IGF-1 LR3 is a different, structurally modified molecule with no authorisation anywhere. Conflating the two is the commonest factual error on this topic.
Cited in: IGF-1 LR3
- Trial registryCitation not yet verified
International Clinical Trials Registry Platform (opens trialsearch.who.int in a new tab)
World Health Organization · accessed 17 August 2026
- Primary research
Koeth RA, et al.. Nature Medicine, 2013
Cited in: L-Carnitine
- Primary researchCitation not yet verified
Acta Paediatrica Supplement, 1993 · doi:10.1111/j.1651-2227.1993.tb12830.x (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Sermorelin
- Primary research
Sikich L, et al.. New England Journal of Medicine, 2021 · doi:10.1056/NEJMoa2103583 (opens doi.org in a new tab)
The largest and longest trial of oxytocin outside obstetrics, and null on its primary outcome.
Cited in: Oxytocin
- Primary researchCitation not yet verified
Ipamorelin, the first selective growth hormone secretagogue (opens doi.org in a new tab)
Raun K, Hansen BS, Johansen NL, et al.. European Journal of Endocrinology, 1998 · doi:10.1530/eje.0.1390552 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Ipamorelin
- Trial registryCitation not yet verified
ISRCTN registry (opens isrctn.com in a new tab)
BMC · accessed 17 August 2026
Cited in: Illustrative Compound ALPHA-1
- Reporting standardCitation not yet verified
International Union of Pure and Applied Chemistry · accessed 17 August 2026
Standard nomenclature for amino acid and peptide description.
Cited in: What is a peptide?
- Regulator or official body
electronic Medicines Compendium, 2023 · accessed 22 August 2026
Legal category: prescription-only medicine; licensed for primary and secondary carnitine deficiency. The injectable presentation (Carnitor Injection, PL 45043/0110) is likewise prescription-only — PL number confirmed against the MHRA products register 20 August 2026.
Cited in: L-Carnitine
- Primary researchCitation not yet verified
Dunaiski V, Dunshea FR, Walton PE, et al.. Journal of Endocrinology, 1997 · doi:10.1677/joe.0.1550559 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: IGF-1 LR3
- Primary researchCitation not yet verified
Conlon MA, Tomas FM, Owens PC, et al.. Journal of Endocrinology, 1995 · doi:10.1677/joe.0.1460247 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: IGF-1 LR3
- Primary researchCitation not yet verified
Cell Metabolism, 2016 · doi:10.1016/j.cmet.2016.09.013 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: NAD+
- Primary researchCitation not yet verified
Genetics in Medicine, 2024 · doi:10.1016/j.gim.2024.101138 (opens doi.org in a new tab)
Uncontrolled extension. Bibliographic record confirmed via NCBI E-utilities.
Cited in: SS-31
- Primary research
Coskun T, et al.. Molecular Metabolism, 2018
Cited in: Tirzepatide
- Primary researchCitation not yet verified
Coskun T et al.. Cell Metabolism, 2022 · doi:10.1016/j.cmet.2022.07.013 (opens doi.org in a new tab)
Bibliographic record confirmed via the NCBI E-utilities API; the publisher page was not directly accessible.
Cited in: Retatrutide
- Primary research
Mazdutide versus dulaglutide in Chinese adults with type 2 diabetes (opens doi.org in a new tab)
Guo L, et al.. Nature, 2026 · doi:10.1038/s41586-025-10031-z (opens doi.org in a new tab)
The only active-comparator phase 3 trial.
Cited in: Mazdutide
- Review or secondary source
Mazdutide: first approval (opens doi.org in a new tab)
Shirley M. Drugs, 2025 · doi:10.1007/s40265-025-02249-y (opens doi.org in a new tab)
Records the Chinese approvals and the absence of any other.
Cited in: Mazdutide
- Primary researchCitation not yet verified
Fornaro M, et al.. American Journal of Physiology: Endocrinology and Metabolism, 2014 · doi:10.1152/ajpendo.00408.2013 (opens doi.org in a new tab)
The replication failure. Bibliographic record confirmed via Europe PMC and the DOI verified as registered via Crossref.
- Regulator or official bodyCitation not yet verified
Medicines and Healthcare products Regulatory Agency (opens gov.uk in a new tab)
GOV.UK · accessed 17 August 2026
The UK regulator for medicines and medical devices. The starting point for any question about the status of a product in the UK.
- Primary research
Kannengiesser K, Maaser C, Heidemann J, et al.. Inflammatory Bowel Diseases, 2008 · doi:10.1002/ibd.20334 (opens doi.org in a new tab)
Cited in: KPV
- Primary research
Nelson ME, et al.. Clinical Toxicology, 2012 · doi:10.3109/15563650.2012.740637 (opens doi.org in a new tab)
Cited in: Melanotan II
- Primary research
Yassin Alsabbagh A, et al.. International Journal of Oral and Maxillofacial Surgery, 2025 · doi:10.1016/j.ijom.2025.03.014 (opens doi.org in a new tab)
Cited in: Melanotan II
- Regulator or official body
electronic Medicines Compendium, 2022 · accessed 22 August 2026
PL 03194/0074, Ferring Pharmaceuticals Ltd. Legal category: prescription-only medicine. Active substance menotrophin, 75 IU FSH and 75 IU LH bioactivity per vial.
Cited in: HMG
- Primary research
Falutz J, et al.. New England Journal of Medicine, 2007
Cited in: Tesamorelin
- Regulator or official bodyCitation not yet verified
MHRA Products portal (opens products.mhra.gov.uk in a new tab)
MHRA · accessed 17 August 2026
Searchable record of products authorised in the UK, including the patient information leaflet and summary of product characteristics.
- Review or secondary source
Théry C, et al.. Journal of Extracellular Vesicles, 2018
Cited in: Exosome-related material
- Review or secondary sourceCitation not yet verified
Rejdak K, Sienkiewicz-Jarosz H, Bienkowski P, et al.. Medicinal Research Reviews, 2023 · doi:10.1002/med.21960 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not separately confirmed.
Cited in: Cerebrolysin
- Primary research
Reynolds JC, Lai RW, Woodhead JST, et al.. Nature Communications, 2021
Cited in: MOTS-c
- Regulator or official body
electronic Medicines Compendium, 2024 · accessed 22 August 2026
Active substance tirzepatide; marketing authorisation holder Eli Lilly and Company Limited. Legal category: prescription-only medicine. Licensed for type 2 diabetes and for weight management alongside diet and physical activity.
Cited in: Tirzepatide
- Review or secondary sourceCitation not yet verified
Gallagher C, Emmanuel OO. Ageing Research Reviews, 2026 · doi:10.1016/j.arr.2026.103057 (opens doi.org in a new tab)
States that no eligible outcomes trial evaluated intravenous or intramuscular NAD+ itself. Bibliographic record confirmed via Europe PMC.
Cited in: NAD+
- GuidanceCitation not yet verified
NHS (opens nhs.uk in a new tab)
NHS · accessed 17 August 2026
For readers seeking health information about themselves rather than information about research.
- Primary researchCitation not yet verified
Trammell SA, Schmidt MS, Weidemann BJ, et al.. Nature Communications, 2016 · doi:10.1038/ncomms12948 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: NAD+
- Regulator or official body
No summer shortcut for safe weight loss (opens gov.uk in a new tab)
Medicines and Healthcare products Regulatory Agency, 2026 · accessed 19 August 2026
States that retatrutide has not been authorised for use in the UK, and that products sold under the name have not been tested for safety, quality or effectiveness.
Cited in: Retatrutide
- Primary researchCitation not yet verified
Francis GL, Ross M, Ballard FJ, et al.. Journal of Molecular Endocrinology, 1992 · doi:10.1677/jme.0.0080213 (opens doi.org in a new tab)
The founding characterisation paper. Bibliographic record confirmed via Europe PMC; the publisher page returned an access error.
Cited in: IGF-1 LR3
- Primary researchCitation not yet verified
Lau DCW et al.. The Lancet, 2021 · doi:10.1016/S0140-6736(21)01751-7 (opens doi.org in a new tab)
Bibliographic record confirmed via the NCBI E-utilities API; the publisher page was not directly accessible.
Cited in: Cagrilintide
- Primary research
Once-weekly mazdutide in Chinese adults with obesity or overweight (opens doi.org in a new tab)
Ji L, et al.. New England Journal of Medicine, 2025 · doi:10.1056/NEJMoa2411528 (opens doi.org in a new tab)
Cited in: Mazdutide
- Primary research
Wilding JPH, et al.. New England Journal of Medicine, 2021
STEP 1, 1,961 participants, 68 weeks.
Cited in: Semaglutide
- Primary research
Haruta I, Fuku Y, Kinoshita K, et al.. Journal of Cachexia, Sarcopenia and Muscle, 2015 · doi:10.1002/jcsm.12028 (opens doi.org in a new tab)
A single patient.
Cited in: GHRP-2
- Review or secondary source
Wang H, et al.. Cochrane Database of Systematic Reviews, 2018
Cited in: Vitamin B12
- Primary research
Xiao B, Xu Z, Viennois E, et al.. Molecular Therapy, 2017 · doi:10.1016/j.ymthe.2016.11.020 (opens doi.org in a new tab)
Cited in: KPV
- Regulator or official body
electronic Medicines Compendium, 2023 · accessed 22 August 2026
PLGB 11648/0273, Merck Serono Ltd. Legal category: prescription-only medicine. Active substance choriogonadotropin alfa (recombinant hCG).
Cited in: HCG
- Regulator or official body
electronic Medicines Compendium, 2016 · accessed 20 August 2026
Cited as a worked example of glacial acetic acid appearing as an authorised pH-adjusting excipient in a UK injectable.
Cited in: Acetic acid solution, Oxytocin
- Primary research
Dalmasso G, Charrier-Hisamuddin L, Nguyen HTT, et al.. Gastroenterology, 2008 · doi:10.1053/j.gastro.2007.10.026 (opens doi.org in a new tab)
Cited in: KPV
- Review or secondary source
Tewari K, Liu TP, Im C, et al.. American Journal of Sports Medicine, 2026 · doi:10.1177/03635465261464420 (opens doi.org in a new tab)
Discusses the constituents individually, as does every review located. None studies the mixture.
Cited in: Glow combination
- Review or secondary source
Vyunova TV, Andreeva L, Shevchenko K, et al.. Protein and Peptide Letters, 2018
Cited in: Selank
- Primary researchCitation not yet verified
Peptides of pineal gland and thymus prolong human life (opens pubmed.ncbi.nlm.nih.gov in a new tab)
Khavinson VKh, Morozov VG. Neuro Endocrinology Letters, 2003
Bibliographic record confirmed via Europe PMC; the article page was blocked to automated retrieval.
Cited in: Thymalin
- Primary research
Takayanagi Y, et al.. Proceedings of the National Academy of Sciences, 2005 · doi:10.1073/pnas.0505312102 (opens doi.org in a new tab)
Cited in: Oxytocin
- Review or secondary source
Harmar AJ, et al.. British Journal of Pharmacology, 2012
Cited in: VIP
- Primary researchCitation not yet verified
Mu X, Qu L, Yin L, et al.. Frontiers in Pharmacology, 2024 · doi:10.3389/fphar.2024.1439536 (opens doi.org in a new tab)
Tested a fusion construct rather than the peptide itself. Bibliographic record confirmed via Europe PMC.
Cited in: DSIP
- Primary research
Khavinson V, Razumovsky M, Trofimova S, et al.. Neuro Endocrinology Letters, 2002
Unregistered, with no described randomisation or blinding.
Cited in: Epitalon
- Primary researchCitation not yet verified
Khavinson V, Ribakova Y, Kulebiakin K, et al.. Rejuvenation Research, 2011 · doi:10.1089/rej.2011.1172 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Pinealon
- Primary researchCitation not yet verified
Arutjunyan A, Kozina L, Stvolinskiy S, et al.. International Journal of Clinical and Experimental Medicine, 2012
Bibliographic record confirmed via Europe PMC.
Cited in: Pinealon
- Primary research
Said SI, Mutt V. Science, 1970
Cited in: VIP
- Review or secondary sourceCitation not yet verified
Drugs in R&D, 2004 · doi:10.2165/00126839-200405040-00011 (opens doi.org in a new tab)
Records the Japanese approval as a diagnostic agent. Bibliographic record confirmed via Europe PMC.
Cited in: GHRP-2
- Primary research
Xu C, Sun L, Ren F, et al.. Regulatory Toxicology and Pharmacology, 2020 · doi:10.1016/j.yrtph.2020.104665 (opens doi.org in a new tab)
Cited in: BPC-157
- Primary researchCitation not yet verified
Teichman SL, Neale A, Lawrence B, et al.. Journal of Clinical Endocrinology and Metabolism, 2006 · doi:10.1210/jc.2005-1536 (opens doi.org in a new tab)
Single-agent, and only for the long-acting form. Bibliographic record confirmed via Europe PMC.
Cited in: CJC-1295 and ipamorelin combination, CJC-1295 with DAC
- Review or secondary source
Salati JA, et al.. Cochrane Database of Systematic Reviews, 2019 · doi:10.1002/14651858.CD001808.pub3 (opens doi.org in a new tab)
Cited in: Oxytocin
- Primary researchCitation not yet verified
Beck DE, Sweeney WB, McCarter MD. International Journal of Colorectal Disease, 2014 · doi:10.1007/s00384-014-2030-8 (opens doi.org in a new tab)
Single-agent, and did not lead to approval. Bibliographic record confirmed via Europe PMC.
Cited in: CJC-1295 and ipamorelin combination, Ipamorelin
- Primary researchCitation not yet verified
PubMed (opens pubmed.ncbi.nlm.nih.gov in a new tab)
National Library of Medicine · accessed 17 August 2026
Included to demonstrate citation formatting. A real profile cites specific papers, not a search portal.
Cited in: Illustrative Compound ALPHA-1, What is a peptide?
- Primary researchCitation not yet verified
Ionescu M, Frohman LA. Journal of Clinical Endocrinology and Metabolism, 2006 · doi:10.1210/jc.2006-1702 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: CJC-1295 with DAC
- Primary research
Richie JP Jr, et al.. European Journal of Nutrition, 2015
Cited in: Glutathione
- Review or secondary source
van Wely M, et al.. Cochrane Database of Systematic Reviews, 2011
42 trials, 9,606 couples; no substantive difference in live birth.
Cited in: HMG
- Review or secondary source
Pickart L, Margolina A. International Journal of Molecular Sciences, 2018
Authored by the compound’s principal proponent, who holds commercial interests in it. Read accordingly.
Cited in: GHK-Cu
- Regulator or official body
Regulated products register: acetic acid (E 260) (opens data.food.gov.uk in a new tab)
Food Standards Agency, 2020 · accessed 20 August 2026
Authorised as a food additive in Great Britain with effect from 31 December 2020.
Cited in: Acetic acid solution
- Regulator or official body
Office for Product Safety and Standards · accessed 20 August 2026
Under the INCI name Copper Tripeptide-1 this substance is used in topical cosmetics, which require notification rather than a marketing authorisation. The statutory guidance is explicit that products intended to be ingested, inhaled, injected or implanted are not cosmetic products, so injectable preparations fall outside that regime and hold no UK authorisation.
Cited in: GHK-Cu
- Primary researchCitation not yet verified
Stem Cell Reviews and Reports, 2021 · doi:10.1007/s12015-020-10087-6 (opens doi.org in a new tab)
Non-randomised. Bibliographic record confirmed via Europe PMC.
Cited in: Thymalin
- Primary research
Sosne G, et al.. International Journal of Molecular Sciences, 2023 · doi:10.3390/ijms24010554 (opens doi.org in a new tab)
Cited in: TB-500
- Review or secondary source
Mendias CL, Awan TM. Sports Medicine, 2026 · doi:10.1007/s40279-026-02437-0 (opens doi.org in a new tab)
The peer-reviewed companion to the sample-quality analysis. Concludes that rigorous human safety data are scarce across this class.
Cited in: BPC-157 and TB-500 combination, Glow combination, Klow combination
- Primary research
Moré MI, Kenley D. Journal of Endocrinology and Metabolism, 2014 · doi:10.14740/jem213w (opens doi.org in a new tab)
The source of the self-affirmed GRAS claim. Sponsor-affiliated authorship.
Cited in: AOD-9604
- Primary research
Safety and Tolerability of the Hexadecapeptide AOD9604 in Humans (opens doi.org in a new tab)
Stier H, Vos E, Kenley D. Journal of Endocrinology and Metabolism, 2013 · doi:10.4021/jem157w (opens doi.org in a new tab)
Sponsor-affiliated authorship. Note that this paper is frequently miscited to the Journal of Obesity, which did not publish it.
Cited in: AOD-9604
- Guidance
Cosmetic Ingredient Review · accessed 20 August 2026
Contains no entry for this compound, which is why no safety assessment can be cited for it.
Cited in: AHK-Cu
- Review or secondary source
Strilciuc S, Vécsei L, Boering D, et al.. Pharmaceuticals, 2021 · doi:10.3390/ph14121297 (opens doi.org in a new tab)
Reached a more reassuring safety conclusion than Cochrane on a broadly overlapping evidence base. Declared no external funding.
Cited in: Cerebrolysin
- Primary research
Lee E, Burgess K. Alternative Therapies in Health and Medicine, 2025
Two participants. Reported as a pilot, not a controlled safety study.
Cited in: BPC-157
- Regulator or official body
Search of the electronic Medicines Compendium for cagrilintide (opens medicines.org.uk in a new tab)
electronic Medicines Compendium · accessed 19 August 2026
Returns no results. The compendium holds UK product information for authorised medicines, so the absence of an entry indicates no UK marketing authorisation exists. No MHRA document naming cagrilintide was found, so this record rests on absence from the register rather than on an affirmative regulator statement.
Cited in: Cagrilintide
- Regulator or official body
Search of the electronic Medicines Compendium for retatrutide (opens medicines.org.uk in a new tab)
electronic Medicines Compendium · accessed 19 August 2026
Returns no results, corroborating the absence of any UK product information for this compound.
Cited in: Retatrutide
- Primary researchCitation not yet verified
Neelakantan H, et al.. Biochemical Pharmacology, 2018 · doi:10.1016/j.bcp.2017.11.007 (opens doi.org in a new tab)
The foundational obesity paper. Refers to a class of inhibitors rather than naming this compound specifically. Bibliographic record confirmed via Europe PMC.
Cited in: 5-amino-1MQ
- Primary research
Marso SP, et al.. New England Journal of Medicine, 2016
SUSTAIN-6.
Cited in: Semaglutide
- Primary research
Frontiers in Bioengineering and Biotechnology, 2021 · doi:10.3389/fbioe.2021.677576 (opens doi.org in a new tab)
Independent group, primary human cells.
Cited in: FOXO4-DRI
- Primary researchCitation not yet verified
Kraskovskaya N, Linkova N, Sakhenberg E, et al.. International Journal of Molecular Sciences, 2024 · doi:10.3390/ijms252111363 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Pinealon
- Primary research
Matsuo H, et al.. Biochemical and Biophysical Research Communications, 1971
Cited in: Gonadorelin
- Primary researchCitation not yet verified
Neelakantan H, et al.. Journal of Medicinal Chemistry, 2017 · doi:10.1021/acs.jmedchem.7b00389 (opens doi.org in a new tab)
Bibliographic record and abstract confirmed via Europe PMC; the publisher page blocks automated access.
Cited in: 5-amino-1MQ
- Primary researchCitation not yet verified
Monti JM, Debellis J, Alterwain P, et al.. International Journal of Clinical Pharmacology Research, 1987
Found no significant differences against baseline or placebo. Bibliographic record confirmed via Europe PMC.
Cited in: DSIP
- Regulator or official body
Supply unlicensed medicinal products (specials) (opens gov.uk in a new tab)
Medicines and Healthcare products Regulatory Agency · accessed 20 August 2026
No UK marketing authorisation exists. Cited for the regulatory terminology distinction: an unlicensed medicine in UK usage is a special manufactured or imported for an individual patient, which this preparation is not.
Cited in: Thymalin
- Regulator or official body
Swissmedic (Swiss Agency for Therapeutic Products), 2024 · accessed 20 August 2026
Published 26 March 2024. States that the ingredients do not match the declaration and vary greatly from pack to pack, that one sample contained only caffeine and another none of the listed ingredients, that no medicinal effect has been scientifically proven, and that the product is not authorised and may not be sold, dispensed or used in Switzerland.
Cited in: Lemon Bottle
- Primary research
Esposito S, Deventer K, Goeman J, et al.. Drug Testing and Analysis, 2012 · doi:10.1002/dta.1402 (opens doi.org in a new tab)
Establishes that material sold as TB-500 is the seven-residue fragment, not full-length thymosin beta-4.
Cited in: BPC-157 and TB-500 combination, Glow combination
- Primary research
Esposito S, Deventer K, Goeman J, et al.. Drug Testing and Analysis, 2012 · doi:10.1002/dta.1402 (opens doi.org in a new tab)
Establishes that material sold as TB-500 is the acetylated fragment, not full-length thymosin beta-4.
Cited in: TB-500
- Primary research
Filippenkov IB, Remizova JA, Stavchansky VV, et al.. Genes, 2023
Cited in: Semax
- Review or secondary source
Berlanga-Acosta J, Abreu-Cruz A, Herrera DGB, et al.. Clinical Medicine Insights: Cardiology, 2017 · doi:10.1177/1179546817694558 (opens doi.org in a new tab)
Cited in: GHRP-6
- Primary researchCitation not yet verified
Wessells H, et al.. Journal of Urology, 1998 · doi:10.1016/s0022-5347(01)62903-3 (opens doi.org in a new tab)
Ten participants. Bibliographic record confirmed via Europe PMC.
Cited in: Melanotan II
- Primary research
Baar MP, et al.. Cell, 2017 · doi:10.1016/j.cell.2017.02.031 (opens doi.org in a new tab)
The originating study. Checked for corrections, errata and expressions of concern; none found.
Cited in: FOXO4-DRI
- Review or secondary source
Kalluri R, LeBleu VS. Science, 2020
Cited in: Exosome-related material
- Review or secondary source
The cardiovascular action of hexarelin (opens pmc.ncbi.nlm.nih.gov in a new tab)
Mao Y, Tokudome T, Kishimoto I. Journal of Geriatric Cardiology, 2014 · doi:10.11909/j.issn.1671-5411.2014.03.007 (opens doi.org in a new tab)
Cited in: Hexarelin
- Primary researchCitation not yet verified
Van den Berghe G, Baxter RC, Weekers F, et al.. Clinical Endocrinology, 2002 · doi:10.1046/j.1365-2265.2002.01255.x (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: GHRP-2
- Primary researchCitation not yet verified
Kolosova LI, Moiseeva AB, Turchaninova LN, et al.. Doklady Biological Sciences, 2002 · doi:10.1023/a:1016098302564 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: Cortagen
- Primary researchCitation not yet verified
Nature Communications, 2025 · doi:10.1038/s41467-025-60844-9 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: FOXO4-DRI
- Primary researchCitation not yet verified
Massoud AF, Hindmarsh PC, Matthews DR, et al.. Clinical Endocrinology, 1996 · doi:10.1046/j.1365-2265.1996.722543.x (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not confirmed.
Cited in: Hexarelin
- Primary research
The effect of tripeptide-copper complex on human hair growth in vitro (opens doi.org in a new tab)
Pyo HK, et al.. Archives of Pharmacal Research, 2007 · doi:10.1007/bf02978833 (opens doi.org in a new tab)
The single study underpinning this compound.
Cited in: AHK-Cu
- Primary research
Heffernan M, et al.. Endocrinology, 2001 · doi:10.1210/endo.142.12.8522 (opens doi.org in a new tab)
Cited in: AOD-9604
- Primary researchCitation not yet verified
Journal of Clinical Endocrinology and Metabolism, 2011 · doi:10.1210/jc.2011-1408 (opens doi.org in a new tab)
Registration confirmed via the Crossref API; the publisher page blocks automated access.
Cited in: Kisspeptin-10
- Primary research
BMJ, 2025 · doi:10.1136/bmj-2024-082583 (opens doi.org in a new tab)
The largest trial of this compound. Found no mortality benefit.
Cited in: Thymosin alpha-1
- Primary research
Gusev EI, Martynov MY, Kostenko EV, et al.. Zhurnal Nevrologii i Psikhiatrii im. S.S. Korsakova, 2018
Russian language.
Cited in: Semax
- Primary research
Critical Care, 2013 · doi:10.1186/cc11932 (opens doi.org in a new tab)
Cited in: Thymosin alpha-1
- Review or secondary source
Dominikowski A, Rękoś Z, Olejarz M, et al.. Frontiers in Endocrinology, 2026 · doi:10.3389/fendo.2026.1822475 (opens doi.org in a new tab)
States that the stacking practice rests on anecdotal rationale, and records that the form usually combined is the one without published human pharmacokinetics.
Cited in: CJC-1295 and ipamorelin combination, CJC-1295 without DAC, Ipamorelin, PEG-MGF
- Primary research
The gasping syndrome and benzyl alcohol poisoning (opens doi.org in a new tab)
Gershanik J, et al.. New England Journal of Medicine, 1982 · doi:10.1056/NEJM198211253072206 (opens doi.org in a new tab)
Cited in: Bacteriostatic water
- Primary researchCitation not yet verified
The GPR54 gene as a regulator of puberty (opens doi.org in a new tab)
New England Journal of Medicine, 2003 · doi:10.1056/NEJMoa035322 (opens doi.org in a new tab)
Registration confirmed via the Crossref API; the publisher page blocks automated access.
Cited in: Kisspeptin-10
- Regulator or official bodyCitation not yet verified
The Human Medicines Regulations 2012 (opens legislation.gov.uk in a new tab)
legislation.gov.uk · accessed 17 August 2026
The principal UK legislation governing medicinal products, including the definition of a medicinal product and restrictions on advertising.
- Regulator or official body
legislation.gov.uk, 2012 · accessed 19 August 2026
A substance presented as having properties for treating disease, or administered to modify a physiological function, is a medicinal product. No product containing this compound holds a UK marketing authorisation.
- Regulator or official body
legislation.gov.uk, 2012 · accessed 20 August 2026
No UK marketing authorisation and no UK novel food authorisation, so there is no lawful route to sale as a food or supplement in Great Britain either.
Cited in: 5-amino-1MQ, Adamax, BPC-157 and TB-500 combination, Cagrilintide and semaglutide combination, Cerebrolysin, CJC-1295 and ipamorelin combination, CJC-1295 with DAC, CJC-1295 without DAC, Cortagen, DSIP, Epitalon, Exosome-related material, FOXO4-DRI, GHRP-2, GHRP-6, Glow combination, Glutathione, Hexarelin, IGF-1 LR3, Ipamorelin, Kisspeptin-10, Klow combination, Lemon Bottle, Lipo-C, LL-37, Mazdutide, Melanotan I, MGF, MOTS-c, PEG-MGF, Pinealon, Selank, Semax, Tesamorelin
- Review or secondary source
Ascoli M, Fanelli F, Segaloff DL. Endocrine Reviews, 2002
Cited in: HCG
- Review or secondary source
Gravina AG, Pellegrino R, Durante T, et al.. Cells, 2023 · doi:10.3390/cells12141889 (opens doi.org in a new tab)
Covers the constituent’s own preclinical base, not the mixture.
Cited in: Klow combination
- Primary research
Journal of Biological Chemistry, 2001 · doi:10.1074/jbc.M104847200 (opens doi.org in a new tab)
Registration and bibliographic detail confirmed via the Crossref API.
Cited in: Kisspeptin-10
- Primary research
Lee C, Zeng J, Drew BG, et al.. Cell Metabolism, 2015
Cited in: MOTS-c
- Primary research
Kumagai H, Natsume T, Kim SJ, et al.. Biochimica et Biophysica Acta — General Subjects, 2022
Cited in: MOTS-c
- Review or secondary source
The oxytocin receptor system: structure, function, and regulation (opens doi.org in a new tab)
Gimpl G, Fahrenholz F. Physiological Reviews, 2001 · doi:10.1152/physrev.2001.81.2.629 (opens doi.org in a new tab)
Cited in: Oxytocin
- Regulator or official bodyCitation not yet verified
The Prohibited List (opens wada-ama.org in a new tab)
World Anti-Doping Agency · accessed 17 August 2026
Relevant to readers in tested sport. The list is revised annually and must be checked against the current edition.
- Primary research
Chang CH, Tsai WC, Lin MS, et al.. Journal of Applied Physiology, 2011 · doi:10.1152/japplphysiol.00945.2010 (opens doi.org in a new tab)
Cited in: BPC-157
- GuidanceCitation not yet verified
The UK Advertising Codes (opens asa.org.uk in a new tab)
Committees of Advertising Practice · accessed 17 August 2026
The CAP and BCAP codes, which govern how medicines and health claims may be advertised in the UK.
- Regulator or official body
Thymalfasin — orphan designation EU/3/02/110 (opens ema.europa.eu in a new tab)
European Medicines Agency, 2002 · accessed 20 August 2026
No UK marketing authorisation exists. The EMA granted only an orphan designation, and the page states plainly that an orphan designation is not a marketing authorisation. Thymalfasin is authorised nationally in Italy, which confers no UK status.
Cited in: Thymosin alpha-1
- Primary researchCitation not yet verified
Blood, 2006 · doi:10.1182/blood-2006-02-004762 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC; the publisher page was not directly accessible.
Cited in: Thymosin alpha-1
- Primary research
Tirzepatide Once Weekly for the Treatment of Obesity (opens pubmed.ncbi.nlm.nih.gov in a new tab)
Jastreboff AM, et al.. New England Journal of Medicine, 2022
SURMOUNT-1, 2,539 participants, 72 weeks.
Cited in: Tirzepatide
- Primary research
Frías JP, et al.. New England Journal of Medicine, 2021
SURPASS-2. The semaglutide comparator was the 1 mg dose.
Cited in: Tirzepatide
- Primary research
Gao L, et al.. JAMA, 2026 · doi:10.1001/jama.2026.8142 (opens doi.org in a new tab)
Source of the adverse-event rates quoted in the safety section.
Cited in: Mazdutide
- Primary researchCitation not yet verified
Grönberg A, Mahlapuu M, Ståhle M, et al.. Wound Repair and Regeneration, 2014 · doi:10.1111/wrr.12211 (opens doi.org in a new tab)
Bibliographic record confirmed via Europe PMC.
Cited in: LL-37
- Primary research
Sanyal AJ et al.. Nature Medicine, 2024 · doi:10.1038/s41591-024-03018-2 (opens doi.org in a new tab)
Cited in: Retatrutide
- Review or secondary source
Casarini L, et al.. Endocrine Reviews, 2018
Cited in: HCG
- GuidanceCitation not yet verified
United Kingdom Accreditation Service (opens ukas.com in a new tab)
UKAS · accessed 17 August 2026
Publishes accreditation schedules showing which methods a laboratory is accredited for.
Cited in: What a certificate of analysis actually shows, Interpreting certificates of analysis, Independent third-party analysis
- Review or secondary source
Vitamin B12 deficiency (opens pubmed.ncbi.nlm.nih.gov in a new tab)
Hunt A, Harrington D, Robinson S. BMJ, 2014
Cited in: Vitamin B12
- Regulator or official body
VYLEESI (bremelanotide) prescribing information (opens dailymed.nlm.nih.gov in a new tab)
DailyMed, US National Library of Medicine, 2019 · accessed 20 August 2026
Approved in the United States for a specific diagnosis in premenopausal women, and explicitly not indicated for postmenopausal women or men. There is no UK marketing authorisation, so United States approval confers no UK status.
Cited in: PT-141
- Regulator or official body
electronic Medicines Compendium, 2020 · accessed 20 August 2026
PL 03551/0077. The preservative-free UK standard, indicated for preparation and dilution of parenteral preparations. Also prescription only — so the classification is not an artefact of the preservative.
Cited in: Bacteriostatic water
- Regulator or official body
electronic Medicines Compendium, 2024 · accessed 22 August 2026
Active substance semaglutide; marketing authorisation holder Novo Nordisk Limited. Legal category: prescription-only medicine. Ozempic and Rybelsus are further licensed presentations of the same active substance.
Cited in: Semaglutide
- Guidance
World Anti-Doping Code International Standard Prohibited List 2026 (opens wada-ama.org in a new tab)
World Anti-Doping Agency, 2026 · accessed 20 August 2026
Section S4.4.1 names this compound explicitly among activators of AMP-activated protein kinase, prohibited at all times both in and out of competition, as a non-specified substance. Read in full from the official document.
- Regulator or official bodyCitation not yet verified
MHRA · accessed 17 August 2026
The UK route for reporting suspected side effects, defective products and falsified medicines.
