Peptide basics
Peptides with falling research activity: where publication counts are dropping
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Counting how many papers name a compound each year shows where research attention is going. On several tracked peptides it is going away.
Selank is the clearest case: 12 PubMed records naming it in 2017-2019, six in 2020-2022, and none at all in 2023-2025. Follistatin 344 also reached zero.
Hexarelin, GHRP-2 and GHRP-6 have each roughly halved over the same decade. None of these compounds has a registered human trial.
A falling count means fewer people are publishing. It does not mean a compound was tested and failed — for these compounds, no human result was ever posted to fail.
This page counts publications and registrations. A declining literature is not a safety finding, an efficacy finding, or a reason to use or avoid anything, and nothing here should be read as one.
The method, so you can repeat it
Each figure below is a count of PubMed records whose title or abstract contains the compound name, within a three-year publication-date window. In PubMed syntax that is the compound name in quotation marks followed by [tiab], combined with a date range in [dp]. Restricting to title and abstract keeps out records that merely cite the term in a reference list, and comparing equal-length windows removes the growth of the database itself from the picture.12
The compounds moving away from zero — downward
Selank: twelve, six, none
Selank returned 12 PubMed records for 2017-2019, six for 2020-2022, and zero for 2023-2025. Three consecutive complete years with no title-or-abstract record at all is the cleanest decline on the site, and it belongs to a compound that draws 6,791 English Wikipedia readers a month.18
The literature that does exist is largely mechanistic and largely Russian in origin — a 2018 review in Protein and Peptide Letters characterises it in exactly those terms, as molecular aspects of the heptapeptide's biological activity. There is no ClinicalTrials.gov record naming Selank as an intervention, and the FDA's compounding assessment states that it lacks important information regarding any safety issues raised by selank acetate administered to humans.367
Follistatin 344: two, two, none
A small literature that became no literature: two records in each of the first two windows, none in 2023-2025. With counts this low the percentage change is meaningless, but the arrival at zero is not — it means nothing naming this compound reached a title or abstract for three years.1
The growth hormone releasing peptides
- GHRP-6: 66 records in 2017-2019, 48 in 2020-2022, 35 in 2023-2025.
- Hexarelin: 18, then 12, then 5.
- GHRP-2: 13, then 8, then 5.
- CJC-1295: 3, then 6, then 3 — a small literature with no trend worth naming.
- Ibutamoren (MK-677): 4, then 12, then 6.1
GHRP-6 is the one to notice. It has the largest literature in this group by a wide margin and it is still shrinking, roughly forty-seven per cent down across the decade. Hexarelin has fallen by around 70% and GHRP-2 by around 60%, both from a much smaller base. None of the five has a registered study naming it as an intervention.13
Melanotan II
16 records in 2017-2019, 29 in 2020-2022, 10 in 2023-2025. The middle window is the anomaly rather than the last one, and the shape is a spike and retreat rather than a steady decline. It is included because the endpoint is genuinely lower than the start, and excluded from the strong claims because a single elevated window is not a trend.1
What a declining count does not establish
The tempting reading is that these compounds were investigated, found wanting, and abandoned. That reading requires a finding, and for every compound on this page there is no registered human trial and therefore no posted human result to have been the finding. Whatever caused researchers to move on, it was not a public negative result about people.3
The ordinary explanations are duller. Funding follows fashion and follows commercial prospects. A compound with no patentable position and no sponsor attracts neither. Laboratories close, principal investigators retire, and small national literatures shrink when the group that sustained them stops. Attrition in drug development is also simply high: an analysis of over 400,000 development-phase records estimated the overall probability of a drug moving from phase 1 to approval in the low double digits, so most things that get studied stop being studied.5
The literature is also a partial view
Publication counts undercount research for a well-documented reason: a large share of completed trials never reach a journal. A cross-sectional analysis of NIH-funded trials registered on ClinicalTrials.gov found fewer than half published in a peer-reviewed journal within 30 months of completion. Silence in the literature therefore travels partly under its own power, independent of what anyone found.4
That cuts against over-reading a decline, and it also cuts against comfort. If research on a compound had continued out of public view, the compounds on this page would still show these counts. The reader's position is unchanged either way: there is progressively less to read, and there was never a registered human trial to read in the first place.34
Does a falling publication count mean a compound was disproved?
No. Disproving something requires a study that produced a result. None of the compounds on this page has a registered human trial, so there is no public human result — positive or negative — behind the decline.
Why compare three-year windows instead of single years?
Because annual counts in the single digits swing wildly on one paper. Three-year buckets of equal length smooth that out and also neutralise the steady growth of PubMed itself, which would otherwise make every compound look busier over time.
Could research be continuing in another language?
Partly. PubMed indexes many non-English journals, but coverage is uneven, and several of these compounds have Russian-language literatures whose indexing is incomplete. A count of PubMed records is a count of what PubMed indexes.
Which compounds are moving the other way?
A separate page covers the compounds where publications and registered trial starts are both rising. The contrast is stark: the accelerating group is almost entirely metabolic chemistry with commercial sponsors.
Sources
- Secondary sourcePubMedNational Center for Biotechnology Information, U.S. National Library of Medicine, 2026pubmed.ncbi.nlm.nih.gov/ ↗↩ Back to text
- Secondary sourceEntrez Programming Utilities HelpNational Center for Biotechnology Information, U.S. National Library of Medicine, 2026www.ncbi.nlm.nih.gov/books/NBK25501/ ↗↩ Back to text
- RegulatoryClinicalTrials.govU.S. National Library of Medicine, National Institutes of Health, 2026clinicaltrials.gov/ ↗↩ Back to text
- Primary studyPublication of NIH funded trials registered in ClinicalTrials.gov: cross sectional analysisRoss JS, Tse T, Zarin DA, Xu H, Zhou L, Krumholz HM. BMJ, 2012 · doi:10.1136/bmj.d7292 · PMID 22214755doi.org/10.1136/bmj.d7292 ↗↩ Back to text
- Primary studyEstimation of clinical trial success rates and related parametersWong CH, Siah KW, Lo AW. Biostatistics, 2019 · doi:10.1093/biostatistics/kxx069 · PMID 29394327doi.org/10.1093/biostatistics/kxx069 ↗↩ Back to text
- RegulatoryCertain Bulk Drug Substances for Use in Compounding that May Present Significant Safety RisksU.S. Food and Drug Administration, 2026www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-subst ↗↩ Back to text
- Secondary sourcePeptide-based Anxiolytics: The Molecular Aspects of Heptapeptide Selank Biological ActivityVyunova TV, Andreeva L, Shevchenko K, Myasoedov N. Protein and Peptide Letters, 2018 · doi:10.2174/0929866525666180925144642 · PMID 30255741doi.org/10.2174/0929866525666180925144642 ↗↩ Back to text
- Secondary sourceWikimedia REST API — English Wikipedia pageviewsWikimedia Foundation, 2026wikimedia.org/api/rest_v1/#/Pageviews%20data ↗↩ Back to text