Peptide Research Reference Library
Independent research data verified direct links only
About This Page
This page is a standalone bibliography of published research on peptides and related compounds. It is not a product page, does not sell or promote any product, and is not linked to any product listing. Every reference below includes a direct, working link to the source (PubMed, PMC, the publishing journal, or for pending clinical trial data not yet in a journal the primary press release or ClinicalTrials.gov record). Content here is provided for general research and educational reference only.
1BPC-157
- 1.
Józwiak M, Bauer M, Kamysz W, Kleczkowska P. "Multifunctionality and Possible Medical Application of the BPC 157 Peptide Literature and Patent Review." Pharmaceuticals. 2025;18(2):185.
https://pubmed.ncbi.nlm.nih.gov/40005999/ - 2.
Vasireddi N, Hahamyan H, Salata MJ, et al. "Emerging Use of BPC-157 in Orthopaedic Sports Medicine: A Systematic Review." Am J Sports Med. 2025.
https://pubmed.ncbi.nlm.nih.gov/40756949/ - 3.
Mateescu DM, et al. "BPC-157 as an Investigational Peptide Therapeutic: Biopharmaceutical Challenges, Formulation Strategies, and Translational Development Barriers." Pharmaceutics. 2026;18(5):625.
https://pubmed.ncbi.nlm.nih.gov/42198317/ - 4.
Lee E, Burgess A. "Safety of Intravenous Infusion of BPC157 in Humans: A Pilot Study." 2025.
https://pubmed.ncbi.nlm.nih.gov/40131143/ - 5.
Sikiric P, Boban Blagaic A, Strbe S, et al. "The Stable Gastric Pentadecapeptide BPC 157: Pleiotropic Beneficial Activity and Its Possible Relations with Neurotransmitter Activity." Pharmaceuticals. 2024;17:461.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11053547/
2TB-500 (Thymosin Beta-4)
- 6.
Mayfield CK, Bolia IK, Feingold CL, et al. "Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians." Am J Sports Med. 2026;54(1):223-229.
https://pubmed.ncbi.nlm.nih.gov/41476424/ - 7.
McGuire F, Hughes E, Maak T, Cushman DM. "Thymosin Beta-4 and TB-500 in Tissue Healing, Regeneration, and Musculoskeletal Repair: A Scoping Review." Appl Sci. 2026;16(12):6202.
https://www.mdpi.com/2076-3417/16/12/6202 - 8.
Malinda KM, Sidhu GS, Mani H, et al. "Thymosin β4 Accelerates Wound Healing." J Invest Dermatol. 1999;113:364-368.
https://pubmed.ncbi.nlm.nih.gov/10469335/ - 9.
Rahaman KA, Muresan AR, Min H, et al. "Simultaneous Quantification of TB-500 and Its Metabolites in In Vitro Experiments and Rats by UHPLC-Q-Exactive Orbitrap MS/MS." J Chromatogr B. 2024;1235:124033.
https://pubmed.ncbi.nlm.nih.gov/38382158/ - 10.
Oliveira KS, Roldão JA. "Synthetic Thymosin β-4 (TB-500): Transforming Healing and Tissue Repair in Dentistry." Conference proceedings review, 2025.
https://static.even3.com/anais/1367936.pdf
3CJC-1295
- 11.
Teichman SL, Neale A, Lawrence B, et al. "Prolonged Stimulation of Growth Hormone (GH) and Insulin-Like Growth Factor I Secretion by CJC-1295, a Long-Acting Analog of GH-Releasing Hormone, in Healthy Adults." J Clin Endocrinol Metab. 2006;91(3):799-805.
https://pubmed.ncbi.nlm.nih.gov/16352683/ - 12.
"Once-Daily Administration of CJC-1295, a Long-Acting Growth Hormone-Releasing Hormone (GHRH) Analog, Normalizes Growth in the GHRH Knockout Mouse."
https://pubmed.ncbi.nlm.nih.gov/16822960/ - 13.
"Pulsatile Secretion of Growth Hormone (GH) Persists During Continuous Stimulation by CJC-1295, a Long-Acting GH-Releasing Hormone Analog." J Clin Endocrinol Metab. 2006;91(12):4792-4797.
https://pubmed.ncbi.nlm.nih.gov/17018654/ - 14.
"Qualitative Identification of Growth Hormone-Releasing Hormones in Human Plasma by Means of Immunoaffinity Purification and LC-HRMS/MS." (anti-doping detection methodology for CJC-1295)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830873/ - 15.
Mayfield CK, et al. "Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians" covers CJC-1295/ipamorelin combination data. Am J Sports Med. 2026.
https://pubmed.ncbi.nlm.nih.gov/41476424/
4Ipamorelin
- 16.
Raun K, Hansen BS, Johansen NL, et al. "Ipamorelin, the First Selective Growth Hormone Secretagogue." Eur J Endocrinol. 1998;139(5):552-561.
https://pubmed.ncbi.nlm.nih.gov/9849822/ - 17.
Venkova K, Mann W, Nelson R, Greenwood-Van Meerveld B. "Efficacy of Ipamorelin, a Novel Ghrelin Mimetic, in a Rodent Model of Postoperative Ileus." J Pharmacol Exp Ther. 2009;329:1110-1116.
https://pubmed.ncbi.nlm.nih.gov/19289567/ - 18.
"Prospective, Randomized, Controlled, Proof-of-Concept Study of the Ghrelin Mimetic Ipamorelin for the Management of Postoperative Ileus in Bowel Resection Patients." Int J Colorectal Dis. 2014. (Phase 2 human trial, NCT00672074)
https://link.springer.com/article/10.1007/s00384-014-2030-8 - 19.
Tack J, Depoortere I, Bisschops R, et al. "Influence of Ghrelin on Interdigestive Gastrointestinal Motility in Humans." Gut. 2006;55(3):327-333.
https://pubmed.ncbi.nlm.nih.gov/16216827/ - 20.
"Ghrelin and Functional Dyspepsia." Review covering ghrelin-receptor agonist prokinetic mechanisms including ipamorelin.
https://pubmed.ncbi.nlm.nih.gov/20721353/
5Semaglutide
- 21.
Wilding JPH, Batterham RL, Calanna S, et al. "Once-Weekly Semaglutide in Adults with Overweight or Obesity" (STEP 1). N Engl J Med. 2021;385(1).
https://www.nejm.org/doi/full/10.1056/NEJMoa2032183 - 22.
Garvey WT, Batterham RL, Bhatta M, et al. "Two-Year Effects of Semaglutide in Adults with Overweight or Obesity: The STEP 5 Trial." Nat Med. 2022.
https://pubmed.ncbi.nlm.nih.gov/36216945/ - 23.
STEP-HFpEF Trial: "Semaglutide in HFpEF Across Obesity Class and by Body Weight Reduction."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504076/ - 24.
Weghuber D, Barrett T, Barrientos-Pérez M, et al. "Once-Weekly Semaglutide in Adolescents with Obesity" (STEP TEENS). N Engl J Med.
https://www.nejm.org/doi/full/10.1056/NEJMoa2208601 - 25.
"Semaglutide for the Treatment of Overweight and Obesity: A Review" (cross-trial summary of STEP 1,2,3,4,5,8). 2022.
https://pubmed.ncbi.nlm.nih.gov/36254579/
6Tirzepatide
- 26.
Jastreboff AM, Aronne LJ, Ahmad NN, et al. "Tirzepatide Once Weekly for the Treatment of Obesity" (SURMOUNT-1). N Engl J Med. 2022;387(3).
https://pubmed.ncbi.nlm.nih.gov/35658024/ - 27.
"Tirzepatide After Intensive Lifestyle Intervention in Adults with Overweight or Obesity" (SURMOUNT-3).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667099/ - 28.
"Weight Reduction Over Time in Tirzepatide-Treated Participants by Early Weight Loss Response: Post Hoc Analysis in SURMOUNT-1." 2025.
https://pubmed.ncbi.nlm.nih.gov/40677091/ - 29.
"Tirzepatide Leads to Weight Reduction in People with Obesity Due to MC4R Deficiency" (SURMOUNT-1 genetic subgroup analysis).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12532586/ - 30.
"The Efficacy and Safety of Tirzepatide in Patients with Diabetes and/or Obesity: Systematic Review and Meta-Analysis of Randomized Clinical Trials." 2025.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12114739/
7Retatrutide
- 31.
"Efficacy and Safety of Retatrutide, a GIP, GLP-1, and Glucagon Receptor Agonist, in People with Type 2 Diabetes and Inadequate Glycaemic Control" (TRANSCEND-T2D-1). Lancet, 2026.
https://www.sciencedirect.com/science/article/abs/pii/S0140673626009670 - 32.
Eli Lilly. "Lilly's Triple Agonist, Retatrutide, Delivered Powerful Weight Loss in Pivotal Phase 3 Obesity Trial" (TRIUMPH-1). May 2026.
https://www.prnewswire.com/news-releases/lillys-triple-agonist-retatrutide-delivered-powerful-weight-loss-in-pivotal-phase-3-obesity-trial-302778859.html - 33.
Jastreboff AM, Kaplan LM, Frías JP, et al. "Triple-Hormone-Receptor Agonist Retatrutide for Obesity A Phase 2 Trial." N Engl J Med. 2023;389(6):514-526.
https://pubmed.ncbi.nlm.nih.gov/37366315/ - 34.
Eli Lilly. "Lilly's Triple Agonist, Retatrutide, Delivered Weight Loss of Up to an Average of 71.2 lbs Along with Substantial Relief from Osteoarthritis Pain" (TRIUMPH-4). Dec 2025.
https://investor.lilly.com/news-releases/news-release-details/lillys-triple-agonist-retatrutide-delivered-weight-loss-average - 35.
ClinicalTrials.gov record for TRIUMPH-4 (retatrutide, obesity/overweight with knee osteoarthritis).
https://clinicaltrials.gov/study/NCT05931367
8NAD+ / NAD+ Precursors (NMN, NR)
- 36.
"The Therapeutic Perspective of NAD+ Precursors in Age-Related Diseases." 2024.
https://pubmed.ncbi.nlm.nih.gov/38340651/ - 37.
"NAD+ Precursor Supplementation in Human Ageing: Clinical Evidence and Challenges." Nat Metab. 2025.
https://pubmed.ncbi.nlm.nih.gov/41083806/ - 38.
Brakedal B, Dölle C, Riemer F, et al. "The NADPARK Study: A Randomized Phase I Trial of Nicotinamide Riboside Supplementation in Parkinson's Disease." Cell Metab. 2022;34(3):396-407.
https://pubmed.ncbi.nlm.nih.gov/35235774/ - 39.
"Towards Personalized Nicotinamide Mononucleotide (NMN) Supplementation: NAD Concentration" dose-ranging RCT, 80 adults.
https://pubmed.ncbi.nlm.nih.gov/38430946/ - 40.
"Effects of NAD+ Precursor Supplementation on Glucose and Lipid Metabolism in Humans: A Meta-Analysis."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932245/
9MOTS-c
- 41.
Lee C, Zeng J, Drew BG, et al. "The Mitochondrial-Derived Peptide MOTS-c Promotes Metabolic Homeostasis and Reduces Obesity and Insulin Resistance." Cell Metab. 2015;21(3):443-454.
https://www.cell.com/cell-metabolism/fulltext/S1550-4131(15)00061-3 - 42.
Kim KH, Son JM, Benayoun BA, Lee C. "The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress." Cell Metab. 2018;28:516-524.
https://www.cell.com/cell-metabolism/fulltext/S1550-4131(18)30390-5 - 43.
"MOTS-c: A Novel Mitochondrial-Derived Peptide Regulating Muscle and Fat Metabolism."
https://pubmed.ncbi.nlm.nih.gov/27216708/ - 44.
"Mitochondria-Derived Peptide MOTS-c: Effects and Mechanisms Related to Stress, Metabolism and Aging."
https://pubmed.ncbi.nlm.nih.gov/36670507/ - 45.
"Mitochondrial-Encoded Peptide MOTS-c Prevents Pancreatic Islet Cell Senescence to Delay Diabetes." Exp Mol Med. 2025.
https://www.nature.com/articles/s12276-025-01521-1
10Epithalon (Epitalon)
- 46.
Khavinson VKh, Bondarev IE, Butyugov AA. "Epithalon Peptide Induces Telomerase Activity and Telomere Elongation in Human Somatic Cells." Bull Exp Biol Med. 2003.
https://pubmed.ncbi.nlm.nih.gov/12937682/ - 47.
"Overview of Epitalon Highly Bioactive Pineal Tetrapeptide with Promising Properties." 2025.
https://pubmed.ncbi.nlm.nih.gov/40141333/ - 48.
"Overview of Epitalon Highly Bioactive Pineal Tetrapeptide with Promising Properties" (open-access version with mechanism figures).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11943447/ - 49.
Korkushko OV, Khavinson VKh, Shatilo VB, Antonyk-Sheglova IA. "Peptide Geroprotector from the Pituitary Gland Inhibits Rapid Aging of Elderly People: Results of 15-Year Follow-Up." (randomized comparative study, epithalamin)
https://pubmed.ncbi.nlm.nih.gov/22451889/ - 50.
Anisimov VN, Khavinson VKh, Popovich IG, et al. "Effect of Epitalon on Biomarkers of Aging, Life Span and Spontaneous Tumor Incidence in Female Swiss-Derived SHR Mice."
https://pubmed.ncbi.nlm.nih.gov/14501183/
11Semax
- 51.
Dolotov OV, Seredenina TS, Levitskaya NG, et al. "The Heptapeptide SEMAX Stimulates BDNF Expression in Different Areas of the Rat Brain In Vivo." Dokl Biol Sci. 2003.
https://pubmed.ncbi.nlm.nih.gov/14556513/ - 52.
Shadrina M, Kolomin T, Agapova T, et al. "Comparison of the Temporary Dynamics of NGF and BDNF Gene Expression in Rat Hippocampus, Frontal Cortex, and Retina Under Semax Action."
https://pubmed.ncbi.nlm.nih.gov/19662538/ - 53.
"[Effect of Semax on the Temporary Dynamics of Brain-Derived Neurotrophic Factor and Nerve Growth Factor Gene Expression in the Rat Hippocampus and Frontal Cortex]."
https://pubmed.ncbi.nlm.nih.gov/18756821/ - 54.
Medvedeva EV, Dmitrieva VG, Povarova OV, et al. "The Peptide Semax Affects the Expression of Genes Related to the Immune and Vascular Systems in Rat Brain Focal Ischemia: Genome-Wide Transcriptional Analysis." BMC Genomics. 2014.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987924/ - 55.
Gusev EI, Martynov MYu, Kostenko EV, Petrova LV, Bobyreva SN. "The Efficacy of Semax in the Treatment of Patients at Different Stages of Ischemic Stroke." Zh Nevrol Psikhiatr. 2018.
https://pubmed.ncbi.nlm.nih.gov/29798983/
12Selank
- 56.
Kolik LG, et al. "Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats." Bull Exp Biol Med.
https://pubmed.ncbi.nlm.nih.gov/36322304/ - 57.
"Functional Connectomic Approach to Studying Selank and Semax Effects." 2020. (fMRI, 52 healthy participants)
https://pubmed.ncbi.nlm.nih.gov/32342318/ - 58.
Volkova A, Shadrina M, Kolomin T, et al. "Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission." Front Pharmacol. 2016;7:31.
https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2016.00031/full - 59.
"GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells." Front Pharmacol. 2017.
https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00089/full - 60.
"Selank Peptide Causes Changes in Gene Expression in the Hippocampus of Rats in the Early Hours After Acute Restraint Stress." Nanobiotechnology Reports.
https://link.springer.com/article/10.1134/S2635167624601335
13IGF-1 LR3
- 61.
Tomas FM, Knowles SE, Owens PC, et al. "Insulin-like Growth Factor-I (IGF-I) and Especially IGF-I Variants Are Anabolic in Dexamethasone-Treated Rats." Biochem J. 1992;282(Pt 1):91-97.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1130894 - 62.
Tomas FM, et al. "Long R3 Insulin-like Growth Factor-I (IGF-I) Infusion Stimulates Organ Growth but Reduces Plasma IGF-I, IGF-II and IGF Binding Protein Concentrations in the Guinea Pig."
https://pubmed.ncbi.nlm.nih.gov/7561636/ - 63.
Tomas FM. "Insulin-like Growth Factor-I (IGF-I) Analogue, LR(3)IGF-I, Ameliorates the Loss of Body Weight but Not of Skeletal Muscle During Food Restriction." Growth Horm IGF Res. 2001;11(2):92-103.
https://pubmed.ncbi.nlm.nih.gov/11472075/ - 64.
"Intranasal Long R3 Insulin-Like Growth Factor-1 Treatment." 2024/2025 study.
https://pubmed.ncbi.nlm.nih.gov/39610283/ - 65.
"Mechanisms of IGF-1-Mediated Regulation of Skeletal Muscle Hypertrophy and Atrophy." Mechanism review covering IGF-1/IGF-1 LR3 signaling pathways.
https://pmc.ncbi.nlm.nih.gov/articles/PMC7564605/
14Tesamorelin
- 66.
"Spotlight on Tesamorelin in HIV-Associated Lipodystrophy." 2011.
https://pubmed.ncbi.nlm.nih.gov/22050344/ - 67.
"Effects of Tesamorelin (TH9507), a Growth Hormone-Releasing Factor Analog, in HIV-Infected Patients with Excess Abdominal Fat: Pooled Analysis of Two Phase 3 Trials with Safety Extension Data."
https://pubmed.ncbi.nlm.nih.gov/20554713/ - 68.
"Effect of Tesamorelin on Visceral Fat and Liver Fat in HIV-Infected Patients with Abdominal Fat Accumulation: A Randomized Clinical Trial."
https://pubmed.ncbi.nlm.nih.gov/25038357/ - 69.
"Reduction in Visceral Adiposity Is Associated with an Improved Metabolic Profile in HIV-Infected Patients Receiving Tesamorelin."
https://pubmed.ncbi.nlm.nih.gov/22495074/ - 70.
"Body Composition, Hepatic Fat, Metabolic, and Safety Outcomes of Tesamorelin: A Meta-Analysis of RCTs." 2026.
https://pubmed.ncbi.nlm.nih.gov/41545261/
15GHK-Cu (Copper Peptide)
- 71.
Maquart FX, Bellon G, Chaqour B, et al. "In Vivo Stimulation of Connective Tissue Accumulation by the Tripeptide-Copper Complex Glycyl-L-Histidyl-L-Lysine-Cu2+ in Rat Experimental Wounds." J Clin Invest. 1993;92:2368-2376.
https://www.jci.org/articles/view/116842 - 72.
"Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data."
https://pmc.ncbi.nlm.nih.gov/articles/PMC6073405/ - 73.
"Skin Regenerative and Anti-Cancer Actions of Copper Peptides."
https://www.mdpi.com/2079-9284/5/2/29 - 74.
"Copper–GHK Increases Integrin Expression and p63 Positivity by Keratinocytes." Arch Dermatol Res.
https://link.springer.com/article/10.1007/s00403-009-0942-x - 75.
"Expression and Activation of Matrix Metalloproteinases in Wounds: Modulation by the Tripeptide–Copper Complex Glycyl-L-Histidyl-L-Lysine-Cu2+."
https://www.sciencedirect.com/science/article/pii/S0022202X15405147
All links verified at time of publication. ObeliskRX is not affiliated with any of the cited authors, journals, or institutions.
