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Methods · Literature record

Research protocols: what the published studies actually used

A page per compound recording the quantities, frequencies and study lengths reported in the published literature — with the model, the population and the limitations attached to every figure.

Read this first

Every figure on this page is a range reported in published literature or in a publicly documented study protocol. It is a record of what researchers used, not a recommendation, a therapeutic protocol, or advice. Peptide Intel Hub is an independent publication, sells nothing, and describes these compounds as in-vitro research reagents only.

Why these pages exist

Most numbers circulating about research peptides have no citation behind them. They are forum figures repeated until they sound official. The purpose of this section is narrower and more useful: for each compound, we go back to the published work and record what was actually administered, to what, how often, and for how long.

That means most of the figures here are per kilogram of rodent body weight, or molar concentrations in culture media, because that is the shape of the evidence. Where a real human trial exists — tesamorelin, thymosin alpha-1, SS-31, PT-141, the incretin class — we say so and give the trial figure. Where it does not, we say that too, plainly.

Reading a range next to its model is the entire point. A figure from a 14-day mouse colitis study is not a protocol; it is a description of one experiment.

Browse A to Z

Swipe across the letters and tap one to jump straight to the compounds starting with it.

Metabolic

Pro-apoptotic peptidomimetic targeting prohibitin in white adipose vasculature

Adipotide · FTPP, Prohibitin-targeting peptidomimetic

Adipotide was developed as an anti-obesity candidate that destroys the blood supply of white adipose tissue rather than acting on appetite. The published record is rodent and non-human primate work; the primate study reported dose-limiting renal toxicity, which is the reason no human programme followed.

2 reported ranges

AMP analogue and AMPK activator (small molecule, not a peptide)

AICAR · Acadesine, AICA riboside

AICAR is a small-molecule AMP mimetic that activates AMPK, the cell's energy-sensing kinase. It has a real human trial history in cardiac surgery and leukaemia, and a well known rodent exercise-mimetic literature. It is a prohibited substance in sport.

2 reported ranges

Long-acting amylin analogue (AMY1 class)

Cagrilintide

Cagrilintide is a long-acting amylin analogue studied mostly in combination with GLP1-class agonists such as semaglutide. Its published protocols follow the same weekly escalation pattern as the incretin class.

2 reported ranges

GLP-1 receptor agonist

GLP1 (semaglutide / Ozempic) · Semaglutide, sold as Ozempic and Wegovy — single GLP-1 receptor agonist

GLP1 is the research code name for semaglutide, sold as Ozempic and Wegovy. This page covers that one compound only, so the reported figures cannot be confused with the dual or triple agonists. Every published programme uses a stepped escalation design rather than a fixed quantity.

1 reported range

Dual GIP/GLP-1 receptor agonist

GLP2 (tirzepatide / Mounjaro) · Tirzepatide, sold as Mounjaro and Zepbound — dual GIP/GLP-1 receptor agonist

GLP2 is the research code name for tirzepatide, sold as Mounjaro and Zepbound. This page covers that one compound only. Its published escalation ladder differs from the single-receptor GLP1 ladder, which is exactly why the two are kept on separate pages.

1 reported range

Triple GIP/GLP-1/glucagon receptor agonist

GLP3 (retatrutide) · Retatrutide — investigational triple GIP/GLP-1/glucagon receptor agonist

GLP3 is the research code name for retatrutide, which remains investigational and has no approved product. This page covers that one compound only, with the phase 2 escalation exactly as it was published.

1 reported range

Quaternary ammonium compound (fatty-acid transport cofactor)

L-Carnitine

L-carnitine is a well-studied nutrient cofactor with a large clinical literature in dialysis, cardiac and exercise-physiology settings. Its figures are unusually well established compared with most compounds in this section.

2 reported ranges

Proprietary cosmetic lipolytic blend (reported: riboflavin, lecithin, bromelain)

Lemon Bottle

Lemon Bottle is a proprietary cosmetic product, not a research compound with a literature. It is included here because it is widely searched alongside genuine research reagents, and the honest answer is that no peer-reviewed pharmacology exists for it.

2 reported ranges

Compounded lipotropic nutrient solution — not a peptide

Lipo-B · Lipotropic B injection (methionine, inositol, choline, B12)

Lipo-B is a compounded mixture of methionine, inositol, choline and cyanocobalamin sold as a lipotropic injection. It is not a peptide and it is not a single studied compound: the evidence base is the separate nutrient literature for each component, and there is no controlled trial of the combination for body composition.

2 reported ranges

Compounded blend — methionine, inositol, choline, usually with B vitamins and L-carnitine

Lipo-C · MIC / lipotropic blend

Lipo-C is a compounded blend rather than a defined molecule, so there is no single literature for it. What exists is evidence for the individual nutrients, plus a notable absence of controlled trials of the blend itself.

2 reported ranges

Single GLP-1 receptor agonist, albumin-binding fatty-acid acylated analogue

Liraglutide · NN2211

Liraglutide is a once-daily GLP-1 receptor agonist and the first of the acylated analogues to carry a large registered trial record in both type 2 diabetes and obesity. It is a distinct compound from semaglutide: shorter acting, dosed daily rather than weekly, and escalated on a different schedule.

2 reported ranges

GLP-1 receptor / glucagon receptor dual agonist (oxyntomodulin analogue)

Mazdutide · IBI362, LY3305677

Mazdutide is an oxyntomodulin-derived dual GLP-1/glucagon receptor agonist developed largely through Chinese phase 2 and phase 3 programmes in obesity and type 2 diabetes. The reported figures below come from those registered protocols.

2 reported ranges

Pan-ERR (estrogen-related receptor) agonist, small molecule

SLU-PP-332

SLU-PP-332 is a small-molecule ERR agonist described as an 'exercise mimetic' in press coverage. The entire published record is mouse work from a small number of laboratories, and no human data exists.

2 reported ranges

Dual glucagon receptor / GLP-1 receptor agonist

Survodutide · BI 456906

Survodutide is an investigational dual glucagon/GLP-1 receptor agonist studied in obesity, type 2 diabetes and metabolic dysfunction-associated steatohepatitis. Unlike most compounds on this site it has a substantial registered human trial record, so the reported figures come from phase 2 protocols rather than animal work.

2 reported ranges

Cobalamin vitamin

Vitamin B12 (cyanocobalamin / methylcobalamin)

B12 has decades of established clinical dosing literature for deficiency and pernicious anaemia. It is included here because it appears constantly as a blend component, where its role and its figures are usually left unstated.

2 reported ranges

Regenerative

11-amino-acid erythropoietin helix-B fragment

ARA-290 · Cibinetide

ARA-290 is a non-erythropoietic fragment of EPO that targets the innate repair receptor. It has completed placebo-controlled human trials in sarcoidosis-associated small-fibre neuropathy, giving it a properly documented human figure.

2 reported ranges

Synthetic pentadecapeptide (gastric origin)

BPC-157

Almost the entire BPC-157 literature is rodent work on tendon, ligament, muscle, nerve and gut injury models. Published quantities are expressed per kilogram of animal body weight, which is why human-equivalent figures circulated online are extrapolations rather than measured values. No controlled human dosing study has been published.

3 reported ranges

Pentadecapeptide + actin-sequestering fragment blend

BPC-157 + TB-500

No peer-reviewed study has tested this specific combination in a controlled design. Blended vials are a commercial format, and any figure quoted for the blend is simply the two single-compound animal ranges placed side by side.

1 reported range

Copper-binding tripeptide

GHK-Cu

GHK-Cu is one of the few peptides in this list with a substantial human literature, and almost all of it is topical dermatology and cosmetic-science work measuring collagen density, wrinkle depth and wound closure.

3 reported ranges

Blend — GHK-Cu, BPC-157 and TB-500

GLOW Blend

GLOW is a commercial three-peptide blend. No study has tested this combination, and one of its components — GHK-Cu — has a literature that is almost entirely topical, which makes its inclusion in an injectable blend a question worth asking.

2 reported ranges

Blend — KPV, GHK-Cu, BPC-157 and TB-500

KLOW Blend

KLOW is GLOW with KPV added. Everything true of the three-peptide blend applies here with one further unstudied component, and the combination has no published evidence of any kind.

2 reported ranges

p53-derived peptide fused to a membrane-penetrating leader sequence

PNC-27

PNC-27 is a laboratory peptide built from a p53 fragment joined to a penetratin-style leader. Published work is dominated by cell-culture assays reporting selective membrane disruption of cancer cell lines. There is no human trial record of any kind.

2 reported ranges

Actin-sequestering peptide fragment

TB-500 · Thymosin Beta-4 fragment

TB-500 is a synthetic fragment of thymosin beta-4. The human trial literature covers full-length TB4 in dermal wound and dry-eye studies, not the fragment sold as a research reagent, so the two evidence bases should be read separately.

2 reported ranges

Growth Hormone

hGH fragment 176-191

AOD-9604

AOD-9604 is the C-terminal fragment of growth hormone, developed as an oral anti-obesity candidate. Its phase 2 programme is public and, importantly, its larger trial did not separate from placebo — an outcome worth as much attention as the protocol.

3 reported ranges

Tetra-substituted GHRH (1-29) analogue

CJC-1295 (no DAC) · Modified GRF (1-29), Mod-GRF 1-29

Without the drug-affinity complex, CJC-1295 is a stabilised GHRH fragment with a short half-life, designed to produce a pulse rather than a sustained elevation. The published record is small — pharmacology studies of GHRH analogue variants rather than a full trial programme.

2 reported ranges

GHRH analogue + selective ghrelin-receptor agonist blend

CJC-1295 (no DAC) + Ipamorelin

The rationale for pairing a GHRH analogue with a secretagogue is documented in pituitary physiology — the two act on different receptors and their combined effect on GH release is more than additive in published pharmacology. What does not exist is a controlled trial of this specific commercial blend.

2 reported ranges

GHRH analogue with albumin-binding drug affinity complex

CJC-1295 with DAC

The DAC version binds serum albumin, which turns a minutes-scale peptide into a week-scale one. This is one of the few secretagogues with published human dose-ranging data measuring sustained IGF-1 elevation.

2 reported ranges

Hexapeptide GH secretagogue

GHRP-2 · Pralmorelin

GHRP-2 is registered in Japan as a diagnostic agent for GH deficiency, which gives it a defined and well-documented human figure — a rarity in this field.

3 reported ranges

Hexapeptide growth-hormone secretagogue

GHRP-6

GHRP-6 has a long pharmacology literature going back to the 1980s, largely as a tool for probing the ghrelin receptor and pituitary GH release. It is notable for provoking a strong appetite response alongside GH release.

2 reported ranges

Synthetic hexapeptide GH secretagogue

Hexarelin

Hexarelin is the most potent of the classic hexapeptide secretagogues and, unusually, has a cardiac literature independent of its GH effects, mediated through CD36 rather than the ghrelin receptor.

3 reported ranges

Recombinant 191-amino-acid human growth hormone

HGH (somatropin, research reference)

Recombinant GH has the deepest clinical literature of anything on this site, spanning paediatric growth disorders, adult deficiency and body-composition research. It is included here as the reference point every secretagogue is implicitly compared against, and it is expressed in international units as often as in milligrams.

3 reported ranges

Modified insulin-like growth factor 1 analogue

IGF-1 LR3 · Long R3 IGF-1

IGF-1 LR3 was engineered as a cell-culture supplement: the modifications reduce binding-protein affinity so it stays active in media. Almost all published quantitative use is in bioreactors and culture, not in whole organisms.

2 reported ranges

Truncated IGF-1 analogue missing the first three N-terminal residues

IGF-DES · DES(1-3) IGF-1

DES(1-3) IGF-1 lacks the first three amino acids of native IGF-1, which sharply reduces binding to IGF binding proteins and makes it substantially more potent in cell assays. Its very short half-life is the defining pharmacokinetic feature and the reason it is studied locally rather than systemically.

2 reported ranges

Selective growth-hormone secretagogue (ghrelin mimetic)

Ipamorelin

Ipamorelin has a genuine early-phase human literature from its development as a post-operative ileus candidate, which is unusual among secretagogues. Those trials measured gastrointestinal motility, with growth-hormone release as a pharmacodynamic marker.

2 reported ranges

Splice variant of IGF-1 produced by mechanically loaded muscle

MGF · Mechano Growth Factor, IGF-1Ec

MGF is the IGF-1Ec splice variant expressed by skeletal muscle after mechanical loading or damage. The literature is largely molecular biology and rodent muscle work examining satellite cell activation; the human evidence base is observational expression data rather than administration studies.

2 reported ranges

Orally active ghrelin mimetic (non-peptide)

MK-677 · Ibutamoren

MK-677 is not a peptide but a small-molecule ghrelin receptor agonist, and it has a real multi-year human trial record from its development programme — including a two-year study in older adults.

2 reported ranges

Polyethylene-glycol conjugated MGF analogue

PEG-MGF · Pegylated Mechano Growth Factor

PEG-MGF is MGF with a polyethylene glycol chain attached to slow renal clearance. The rationale is pharmacokinetic rather than pharmacodynamic — the peptide sequence is the same, the exposure window is longer. The published record is thin and almost entirely preclinical.

1 reported range

GHRH (1-29) analogue

Sermorelin

Sermorelin is the 1-29 fragment of growth-hormone-releasing hormone and was for years a licensed diagnostic agent for paediatric GH deficiency, so its human literature is comparatively solid.

2 reported ranges

Stabilised GHRH analogue

Tesamorelin

Tesamorelin has the largest randomised human dataset of any GHRH analogue, from multi-centre trials measuring visceral adipose tissue by CT scan. Those trials converged on a single figure, which is why the literature here is unusually consistent.

2 reported ranges

Stabilised GHRH analogue + selective secretagogue blend

Tesamorelin + Ipamorelin

This blend pairs the GHRH analogue with the largest randomised dataset in its class with the most selective secretagogue in its class. As with every blend on this site, the combination itself has no published controlled study; only the two constituents do.

2 reported ranges

Hormone

Longevity

Synthetic tripeptide (Ala-Glu-Asp) bioregulator

Cartalax

Cartalax is the cartilage-directed member of the Khavinson short-peptide family, studied for connective-tissue and joint parameters. Like Pinealon and Epithalon, its evidence base is small and regionally concentrated.

2 reported ranges

Synthetic tetrapeptide (Ala-Glu-Asp-Gly)

Epithalon · Epitalon

Epithalon's literature is almost entirely Russian, spanning rodent lifespan studies and long-running human observational cohorts from the St Petersburg Institute of Bioregulation. Independent Western replication is thin, which is the single most important caveat when reading any figure below.

2 reported ranges

FOXO4-p53 interaction-disrupting retro-inverso peptide

FOXO4-DRI

FOXO4-DRI is a senolytic peptide designed to disrupt the FOXO4–p53 interaction and trigger apoptosis selectively in senescent cells. The evidence is a small number of mouse studies from the originating group, with limited independent replication and no human data.

2 reported ranges

Endogenous tripeptide antioxidant (Glu-Cys-Gly)

Glutathione

Glutathione is a well-characterised endogenous tripeptide with clinical literature in Parkinson's disease, chemotherapy-associated neuropathy and dermatology. Oral bioavailability of the standard form is poor, which shapes every protocol.

3 reported ranges

24-amino-acid mitochondrial-derived peptide

Humanin

Humanin was identified in a screen of surviving neurons in Alzheimer's brain tissue and is studied for cytoprotection, insulin sensitivity and neuronal survival. Nearly all quantitative work uses the potentiated analogue HNG rather than native humanin.

2 reported ranges

Mitochondrial-derived peptide (16 amino acids)

MOTS-c

MOTS-c is encoded in mitochondrial DNA and studied for its effects on AMPK signalling, insulin sensitivity and exercise capacity. The literature is rodent and in-vitro; no human dosing trial has been published.

2 reported ranges

Nicotinamide adenine dinucleotide coenzyme

NAD+

Direct NAD+ infusion has a thin trial literature; the substantial evidence sits with its precursors, nicotinamide riboside and nicotinamide mononucleotide, which have multiple randomised human studies.

3 reported ranges

Immune

Cyclic Semax analogue (cyclo-prolylglycine related)

Adamax

Adamax is sold as a modified, more stable Semax analogue. There is effectively no indexed peer-reviewed literature under this name, and that absence is the single most important thing to know about it.

2 reported ranges

α-MSH C-terminal tripeptide

KPV

KPV is the anti-inflammatory C-terminal fragment of α-MSH. The literature is animal colitis and dermatitis models plus in-vitro NF-κB signalling work; there is no published human dosing trial.

2 reported ranges

37-amino-acid cathelicidin antimicrobial peptide

LL-37 · Cathelicidin LL-37

LL-37 is the only human cathelicidin and has a substantial microbiology and wound-healing literature. There is a small but real human study record in venous leg ulcers, which is unusual for a peptide of this type.

3 reported ranges

Thymic peptide extract preparation

Thymalin

Thymalin is a bovine thymic peptide extract used in Russia for decades in immune-modulation research, including long-running observational cohorts in older adults. It is a preparation rather than a defined compound.

2 reported ranges

28-amino-acid thymic peptide

Thymosin Alpha-1

Thymosin alpha-1 has decades of human data from hepatitis B and C trials, sepsis studies and vaccine-adjuvant research, and is a licensed medicine in a number of countries. Its reported figures are unusually stable across studies.

3 reported ranges

28-amino-acid neuropeptide

VIP · Vasoactive intestinal peptide, aviptadil

VIP as aviptadil has been through registered human trials in pulmonary hypertension, sarcoidosis and acute respiratory failure, so its figures are properly documented. Its two-minute half-life explains why almost every protocol is an infusion.

3 reported ranges

Cognitive

Porcine brain-derived peptide preparation

Cerebrolysin

Cerebrolysin is a licensed medicine in a number of countries and has a large trial literature in stroke, traumatic brain injury and dementia. Its figures are stated in millilitres of a standard-concentration solution rather than in milligrams of an active substance.

3 reported ranges

Angiotensin IV analogue, HGF/c-Met potentiator

Dihexa · N-hexanoic-Tyr-Ile-(6) aminohexanoic amide

Dihexa was developed at Washington State University as an orally active angiotensin IV analogue that potentiates hepatocyte growth factor signalling. The record is rodent cognition models and in-vitro synaptogenesis; there is no human data.

2 reported ranges

Nonapeptide

DSIP · Delta sleep-inducing peptide

DSIP was isolated in the 1970s from rabbit cerebral venous blood during induced sleep. The human literature is small, old, and inconsistent — several controlled studies failed to find the sleep effect the name promises.

2 reported ranges

Spadin analogue, TREK-1 channel blocker

PE-22-28

PE-22-28 is a shortened analogue of spadin, studied as a fast-acting antidepressant candidate via TREK-1 potassium channel blockade. All published work is rodent; no human study exists.

2 reported ranges

Synthetic tripeptide (Glu-Asp-Arg) bioregulator

Pinealon

Pinealon belongs to the Khavinson short-peptide bioregulator family, alongside Epithalon and Cartalax. As with the rest of that family, the literature is regionally concentrated, small, and lightly replicated outside its originating institutes.

2 reported ranges

Tuftsin analogue heptapeptide

Selank

Selank was developed in Russia as an anxiolytic peptide and has published human studies in generalised anxiety, mostly intranasal. As with Epithalon, the literature is regionally concentrated and lightly replicated elsewhere.

2 reported ranges

ACTH(4-10) analogue heptapeptide

Semax

Semax is a fragment analogue of ACTH stripped of hormonal activity, studied in Russia for stroke recovery, cognitive performance and optic-nerve conditions. It is a registered medicine there and effectively unstudied in Western trials.

2 reported ranges

ACTH(4-10) analogue + tuftsin analogue blend

Semax + Selank

The two peptides are frequently co-administered in Russian clinical practice, and there are combination reports, but no controlled trial has isolated the effect of the pairing. The figures below are the two source literatures placed side by side.

2 reported ranges

Performance

Cosmetic

Copper-binding tripeptide (Ala-His-Lys)

AHK-Cu

AHK-Cu is the hair-follicle counterpart to GHK-Cu, studied mainly for follicle stimulation and dermal papilla cell proliferation. The literature is smaller and more cosmetic-industry weighted than GHK-Cu's.

2 reported ranges

Linear α-MSH analogue, selective MC1R agonist

Melanotan I · Afamelanotide, Melanotan 1

Melanotan I as afamelanotide completed a full registered development programme for erythropoietic protoporphyria and is an approved medicine in the EU and US. It is the only compound in this cosmetic group with a proper regulatory dossier.

2 reported ranges

Cyclic α-MSH analogue

Melanotan II

Melanotan II has a small early human literature on melanogenesis from the 1990s, after which development stopped. It is also the compound in this list with the most substantial case-report literature describing harms, and that context belongs alongside any figure.

2 reported ranges

Selective MC4R agonist

PT-141 · Bremelanotide

PT-141 completed a full registered development programme and its phase 3 data is public, which makes the reported figures here unusually well characterised for a compound sold as a research peptide.

2 reported ranges

SNAP-25 mimetic octapeptide

Snap-8 · Acetyl octapeptide-3

Snap-8 is a cosmetic-ingredient peptide designed to interfere with SNARE-complex formation, marketed as a topical alternative to neuromodulator injections. Its evidence is manufacturer-sponsored cosmetic testing rather than independent trials.

2 reported ranges

Supplies

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