Peptide Fragments & Analogs

Reference guide to peptide fragments, synthetic analogs, modified versions, and blend formulations — understanding how structural modifications change biological activity.

Peptide Fragments & Analogs

Many research peptides are fragments of larger proteins or synthetic analogs designed to isolate specific biological activities, improve stability, or enhance bioavailability. This category catalogs the relationships between parent molecules and their derivatives.

Complete Peptide Directory

Growth Hormone Fragments

PeptideParent MoleculeModificationResearch Focus
HGH Fragment 176-191Human Growth HormoneC-terminal fragment (residues 176-191)Fat metabolism without GH's growth-promoting effects
AOD-9604HGH Fragment 176-191Stabilized analog with tyrosine additionFat metabolism, osteoarthritis (TGA-approved in Australia)

Thymosin Beta-4 Fragments

PeptideParent MoleculeModificationResearch Focus
TB-500Thymosin Beta-4Active fragment containing actin-binding domainWound healing, cardiac repair, anti-inflammatory
TB-4 FragThymosin Beta-4N-terminal fragment (Ac-SDKP)Anti-fibrotic, anti-inflammatory, cardiovascular
Thymosin Beta-4 SulfoxideThymosin Beta-4Methionine oxidation productDistinct anti-inflammatory profile, glucocorticoid-like effects

Alpha-MSH Fragments & Melanocortin Analogs

PeptideParent MoleculeModificationResearch Focus
Alpha-MSHPOMCEndogenous melanocortin peptide (13 amino acids)Pigmentation, anti-inflammatory, appetite regulation
KPVAlpha-MSHC-terminal tripeptide (residues 11-13)Anti-inflammatory, IBD, NF-kB inhibition
PT-141 (Bremelanotide)Melanotan 2Cyclic heptapeptide; MT-2 metaboliteSexual dysfunction (FDA-approved as Vyleesi)
Melanotan 2Alpha-MSHCyclic analog; non-selective melanocortin agonistTanning, sexual function
Melanotan 1Alpha-MSHLinear analog; selective MC1R agonistPhotoprotection, EPP
MT-II FragmentMelanotan 2Fragment of cyclic melanocortin analogIsolated melanocortin activity research

IGF-1 Analogs

PeptideParent MoleculeModificationResearch Focus
IGF-1EndogenousRecombinant full-lengthGrowth, anabolic effects, neuroprotection
IGF-1 DESIGF-1Truncated (lacks first 3 amino acids)Reduced IGFBP binding; enhanced local tissue effects
IGF-1 LR3IGF-1Arg3 substitution + 13-aa N-terminal extensionGreatly reduced IGFBP binding; extended half-life
Long R3 IGF-1IGF-1Full-length modified for prolonged activityProlonged IGF-1 receptor activation

GHRH Analogs

PeptideParent MoleculeModificationResearch Focus
SermorelinGHRH(1-44)Truncated to first 29 amino acidsGH secretion, anti-aging
CJC-1295GHRH analogModified residues for protease resistanceExtended GH release, body composition
CJC-1295 DACCJC-1295Drug Affinity Complex (albumin-binding)Ultra-long half-life GH stimulation
TesamorelinGHRH(1-44)Trans-3-hexenoic acid modificationHIV lipodystrophy (FDA-approved), visceral fat

ACTH Fragments

PeptideParent MoleculeModificationResearch Focus
SemaxACTH(4-10)C-terminal Pro-Gly-Pro extensionNootropic, neuroprotective, BDNF modulation
SelankTuftsinC-terminal Pro-Gly-Pro extensionAnxiolytic, immunomodulatory, GABA modulation

Cell Cycle & Senescence Peptides

PeptideDescriptionResearch Focus
ARA-290Non-hematopoietic EPO derivative targeting the innate repair receptorNeuropathic pain, tissue repair without erythropoietic effects
B7-33Single-chain relaxin-2 analogRelaxin receptor agonist; anti-fibrotic; cardiovascular
P21 PeptideCNTF-derived peptide for neurogenesisHippocampal neurogenesis; cognitive enhancement
P21-CDK5CDK5 inhibitory peptide based on p35CDK5 inhibition; neuroprotection; tau phosphorylation
P16 Inhibitor PeptidePeptide targeting p16INK4a tumor suppressorSenescence modulation; cell cycle regulation

Common Research Themes

Fragment Advantage: Fragments often isolate a desired biological activity from the parent molecule while eliminating unwanted effects. HGH Fragment 176-191 retains fat metabolism without growth-promoting activity; KPV retains anti-inflammatory effects without melanocortin tanning.

Stability Modifications: PEGylation (PEG-MGF), DAC conjugation (CJC-1295 DAC), N-acetylation, and amidation are common modifications to extend half-life and improve bioavailability of peptides that would otherwise be rapidly degraded.

Synergistic Blending: Blend formulations combine peptides with complementary mechanisms. The most studied synergy is GHRH + GHRP combinations, where GHRH analogs amplify GH pulse amplitude while GHRPs increase pulse frequency.

Getting Started

If you are new to this category, we recommend starting with CJC-1295 / Ipamorelin Blend — the most popular research combination, pairing GHRH and ghrelin receptor pathways for synergistic GH release. From there, explore related peptides through the See Also sections on each page to build a comprehensive understanding of the research landscape.

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