Peptide Protocol Wiki is a comprehensive peptide research database featuring 133+ evidence-based peptide profiles with dosing protocols, mechanism of action breakdowns, and clinical research summaries. Whether you're researching popular compounds like BPC-157, semaglutide, or tirzepatide, exploring growth hormone secretagogues, or comparing peptide options head-to-head, every profile includes peer-reviewed citations you can verify independently. Our free dosing calculator, stack compatibility checker, and 87+ detailed comparisons help you evaluate the current evidence on peptide therapeutics, from GLP-1 receptor agonists and myostatin inhibitors to healing peptides and nootropic compounds.
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CJC-1295 DAC: Long-acting GHRH analog with extended half-life. Covers Drug Affinity Complex mechanism, GH/IGF-1 elevation, dosing, and side effects.
BPC-157 peptide comprehensive research guide. Covers mechanism of action (VEGF, nitric oxide, tendon healing), gut protection, musculoskeletal repair, oral vs injectable research, 2026 FDA reclassification status, safety profile, and clinical trial evidence for this gastric-derived healing peptide.
5-Amino-1MQ is a selective NNMT inhibitor that boosts NAD+ levels. Preclinical data shows anti-obesity and muscle function benefits. No human trials published.
Dihexa (PNB-0408): angiotensin IV-derived peptide that potentiates HGF/c-Met signaling. Covers preclinical cognitive enhancement research, oral bioavailability, and safety considerations.
Glutathione: The body's master antioxidant tripeptide. Covers redox cycling, detoxification, immune support, IV vs oral bioavailability, and dosing.
Apitegromab represents a clear advancement over ACE-031 in myostatin pathway therapeutics. The key lesson from ACE-031 was that broad TGF-beta superfamily inhibition produces unacceptable off-target effects, particularly vascular toxicity. Apitegromab's selective targeting of proMyostatin and latent myostatin addresses this directly, inhibiting only the muscle-relevant pathway while leaving vascular, hematopoietic, and reproductive TGF-beta signaling intact. With an active Phase 3 program and FDA Fast Track designation, apitegromab is positioned as the most clinically advanced selective myostatin inhibitor currently in development.
Afamelanotide and melanotan-1 are the same molecule (Nle4-D-Phe7-alpha-MSH) with different names, regulatory statuses, and delivery systems. Afamelanotide (Scenesse) is the FDA-approved pharmaceutical formulation with proven safety and efficacy from Phase 3 clinical trials, delivered as a controlled-release subcutaneous implant. Melanotan-1 is the unregulated research peptide version available from non-pharmaceutical sources. For EPP patients, afamelanotide is the clearly superior choice as a proven, approved treatment. For individuals seeking tanning or photoprotection outside of EPP, melanotan-1 represents an unregulated alternative with identical pharmacology but unverified product quality and no medical oversight. The core comparison is not between different molecules but between pharmaceutical-grade and research-grade versions of the same peptide.
Aleniglipron and orforglipron are the two leading oral non-peptide small molecule GLP-1 agonists, competing directly for the same market. Aleniglipron's ACCESS Phase 2b data is numerically impressive (11.3% placebo-adjusted at 120 mg in 36 weeks, and up to 15.3% at 240 mg), suggesting it may match or exceed orforglipron's ATTAIN-1 results (12.4% mean at 72 weeks). However, orforglipron is further ahead in development with completed Phase 3, filed FDA submission, and the backing of Eli Lilly. The higher GI event rates with aleniglipron (65% nausea) versus orforglipron's profile are a concern, though dose optimization may improve tolerability. The oral GLP-1 space is poised for intense competition once both agents reach the market.
Alprostadil and PT-141 target fundamentally different aspects of sexual dysfunction and are not direct competitors. Alprostadil is the established choice for male erectile dysfunction, producing reliable erections through direct peripheral vasodilation regardless of the underlying cause. PT-141 addresses the central desire deficit that PDE5 inhibitors and alprostadil cannot reach, making it uniquely relevant for hypoactive sexual desire disorder. The choice depends entirely on the clinical problem — mechanical erectile failure versus diminished sexual desire — and in some cases both mechanisms may be complementary.
Both amycretin and CagriSema are Novo Nordisk programs targeting the same GLP-1 plus amylin dual pathway, but with fundamentally different molecular strategies. CagriSema has the stronger evidence base with completed phase 3 REDEFINE trials showing 20.4% weight loss, and is closer to potential approval. Amycretin offers the elegance of a single molecule activating both pathways, with the critical advantage of an oral formulation and phase 1b/2a data showing up to 24% weight loss at 36 weeks. If amycretin's early data holds in phase 3, its oral availability could make it the preferred option. CagriSema's advantage is the ability to independently optimize the dose of each component.
Amycretin shows potentially superior weight loss (up to 24.3% in Phase 1b/2a) compared to semaglutide (14.9% in STEP 1), driven by its dual GLP-1/amylin mechanism in a single molecule. The ability to offer both injectable and oral formulations without fasting restrictions is a significant advantage. However, these are early-phase results with small sample sizes and short duration. Semaglutide remains the proven, FDA-approved standard with cardiovascular benefit and extensive safety data. Amycretin is Novo Nordisk's most promising pipeline asset, but Phase 3 confirmation is needed before definitive comparisons can be made.
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Peptides are short chains of amino acids (typically 2-50) linked by peptide bonds. They serve as signaling molecules in the body, regulating processes like growth hormone release, immune response, tissue repair, and metabolism. Many peptides are being studied as potential therapeutics.
Use our Peptide Finder quiz to match peptides to your research goals, or browse the full directory filtered by category, evidence level, and research status. Each profile includes dosing protocols, mechanism of action, clinical evidence, and safety data.
Yes. Every peptide profile includes citations to peer-reviewed research. We summarize clinical trials, preclinical studies, and systematic reviews, and link directly to PubMed and DOI sources so you can verify claims independently.
We offer 18 free interactive tools including a dosing calculator, reconstitution guide, peptide stack compatibility checker, evidence explorer, protocol schedule builder, half-life comparison chart, and more. All tools are free to use with no account required.
Content is continuously updated as new research is published. Each peptide profile includes a last-updated date, and our editorial process incorporates new clinical trial results, FDA decisions, and safety data as they become available.