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Research Library

Peptide Names Decoded: Where BPC-157, TB-500, GHRP-6 and -relin Come From

A stack of white cards with text on a light wooden surface

Peptide names look arbitrary until you know which system produced them. A single research catalogue mixes at least three: International Nonproprietary Names chosen through the World Health Organization, code names coined inside a company or laboratory, and names that simply spell out part of a sequence. Each tells you something different, and none of them, on its own, tells you what is in a vial.

This hub explains how each system works, where well-known research names come from when a primary source confirms it, and where the usual explanation is folklore. For the molecules themselves, start with what peptides are; the compound guides linked below go deeper on individual histories.

The short answer

  • Three systems produce most peptide names. WHO International Nonproprietary Names (INNs) built from stems, developer code names, and descriptive or sequence-based names.
  • An INN is a public, global name. WHO calls each INN “a unique name that is globally recognized and is public property”; pralmorelin is an INN, GHRP-2 is not.
  • Stems mark a family, not a sequence. In WHO’s words, “Stems define the pharmacologically related group to which the INN belongs”; -relin marks “pituitary hormone-release stimulating peptides”.
  • Stems are revised. A WHO addendum published in February 2026 changed -morelin from growth hormone release-stimulating “peptides” to “substances”.
  • Code names are laboratory labels. CJC-1295 came from ConjuChem in Montréal, and Metabolic Pharmaceuticals funded the published AOD9604 trials; in the sources we checked, the numbers have no published meaning.
  • A historical name is not a property. BPC is usually expanded as “body protection compound”, a label from the early 1990s, not a description of anything the peptide has been shown to do.
  • A name is not an identity. A product sold as TB-500 was reported in 2012 to contain a seven-residue acetylated fragment of thymosin beta-4, a different molecule from the 43-residue natural peptide; sequence, formula and mass settle identity.

International Nonproprietary Name (INN)

Generic name · WHO INN · the public name of a pharmaceutical substance

What it is
A unique, non-proprietary name for one pharmaceutical substance
Who selects it
WHO’s INN Programme, which publishes proposed and recommended INNs in WHO Drug Information
How it is built
Where possible, a distinctive prefix plus a stem naming the pharmacological group
Peptide stems
-tide, -relin, -morelin, -glutide, -lintide and others
Salts
Names differ only in the inactive part, as in WHO’s example oxacillin sodium
National names
BAN, DCF, JAN and USAN match INNs with rare exceptions, such as leuprolide (USAN) for leuprorelin
What it is not
A trade name, a sequence, or evidence about any particular vial

What a peptide name can tell you

  1. Which substance a seller intends
  2. For an INN, its pharmacological family
  3. The sequence, caps and salt in a vial
  4. Anything about effects

Names point; analysis confirms. Even an INN describes a substance, not the contents of a particular vial.

Why peptide names come in layers

Take GHRP-2, a six-residue growth hormone-releasing peptide. It is GHRP-2 in research catalogues; pralmorelin as an INN; KP-102 as a development code; pralmorelin dihydrochloride under its US adopted name and pralmorelin hydrochloride under its Japanese one, with the trade name GHRP; and it has at least two CAS Registry Numbers, 158861-67-7 for the peptide and 158827-34-0 for the dihydrochloride (PubChem; KEGG). Every one of those names refers to the same chain, D-Ala-D-2Nal-Ala-Trp-D-Phe-Lys-NH2.

The layers exist because different people needed a name at different times: chemists naming a series, a company tracking a candidate, regulators needing one public name per substance and registries needing a number for each form. Knowing which layer a name comes from tells you how much weight it can bear.

Three naming systems, one molecule Three boxes across the top show the naming systems. WHO INN, example sermorelin: a prefix plus the stem -morelin, which names a pharmacological family, not a sequence. Developer code, example CJC-1295: company or project letters plus a series number whose meaning is rarely published. Sequence name, example LL-37: the first residues, Leu-Leu, plus the length, 37 residues. Arrows lead to one molecule, defined by sequence, end caps, bridges and counter-ion and checked against formula, mass and a matching certificate. A dashed note says market names such as TB-500 have no documented place in these systems. Three naming systems, one molecule WHO INN sermorelin prefix + stem -morelin stem = pharmacological family, not a sequence Developer code CJC-1295 company or project letters + series number meaning rarely published Sequence name LL-37 first residues: Leu-Leu + length: 37 residues decodes to a sequence One molecule sequence + end caps + bridges + counter-ion checked against formula, mass and a matching certificate Market names, such as TB-500, have no documented place in these systems and may not point to a single molecule.
Schematic. Each naming system answers a different question about a peptide; none replaces the sequence, formula and mass.

A name points you to a molecule; the sequence confirms it. See how to read sequence notation.

Read sequence notation

International Nonproprietary Names and WHO stems

WHO’s INN Programme selects one generic name per pharmaceutical substance, and “Each INN is a unique name that is globally recognized and is public property.” Related substances are meant to look related, because “Stems define the pharmacologically related group to which the INN belongs.” The table gives WHO’s definitions of the INN stems that matter most in a research catalogue, with examples confirmed in KEGG, PubChem or WHO’s own lists. Our growth hormone peptides research map shows how the -relin family fits together.

StemWHO definitionExamples
-tide“peptides and glycopeptides (for special groups of peptides see -actide, -pressin, -relin, -tocin)”The parent stem for most peptide INNs
-relin“pituitary hormone-release stimulating peptides”gonadorelin, protirelin
-morelin“growth hormone release-stimulating substances” since February 2026; previously “peptides”sermorelin, pralmorelin (GHRP-2), ipamorelin
-glutide“glucagon-like peptide (GLP) analogues and agonists”, widened from “analogues” in the 2018 stem bookliraglutide, teduglutide
-lintide“amylin receptor agonists including dual amylin / calcitonin receptor agonists”pramlintide, cagrilintide
-patide“gastric inhibitory polypeptide (glucose-dependent insulinotropic polypeptide, GIP) receptor agonists with or without GLP-1 receptor agonist activity”tirzepatide
-dutide“oxyntomodulin analogues and other dual agonists at glucagon-like peptide receptor 1 (GLP-1R) and glucagon receptors (GCGR)”mazdutide, survodutide
-trutide (pre-stem)“antihyperglycaemic triple agonist peptides”retatrutide (US adopted name)

Three cautions apply to peptide naming by stem. Stems can be redefined: the February 2026 addendum widened -morelin from “peptides” to “substances” without stating why, and an earlier addendum widened -glutide to “analogues and agonists”. Pre-stems are provisional; WHO describes a pre-stem as “similar to stem, but it didn’t reach the stage of stem yet”. And national names usually, not always, match: WHO says British, French, Japanese and US names “are nowadays, with rare exceptions, identical to the INNs”, yet the INN leuprorelin is leuprolide under its US adopted name. Salts add a layer of their own: KEGG lists sermorelin (INN) and sermorelin acetate (USAN) separately.

Developer code names: letters, numbers and history

Before a molecule gets an INN, if it ever does, it is tracked by a code: letters for a company, institute or project and a number from an internal series. Peptide code names help when searching old papers and patents, but their meanings are rarely published, and a guessed expansion repeated as fact is how folklore starts.

CJC-1295 was developed at ConjuChem in Montréal: the 2005 paper that identified it among albumin conjugates of hGRF(1–29) came from the company’s research department, and three authors of a 2006 paper on the compound were at ConjuChem, Inc. The letters match the company name, but we found no ConjuChem document spelling out the prefix, and nothing explains the number. The name first belonged to that albumin-binding analogue; “CJC-1295 without DAC” is a market label for a different molecule that lacks the albumin-binding group.

AOD9604 is “Tyr-hGH177-191”, residues 177–191 of human growth hormone with an added N-terminal tyrosine; the published safety paper, one of whose authors was at Metabolic Pharmaceuticals, thanks the company for “funding all six clinical trials”. AOD is often expanded as “anti-obesity drug”, but that paper never spells the letters out, and we could not confirm the expansion in a primary source, so regard it as reported rather than established. Our AOD-9604 guide covers the research history.

BPC 157 is the case where the expansion is documented and the number is not. A 2025 literature and patent review describes it as “known as the ‘Body Protection Compound’”, a pentadecapeptide isolated from human gastric juice, first described by Sikirić and colleagues in 1993 and also known as PLD-116, PL-10, PL14736 or Bepectin. “Body protection” is a historical name, not a demonstrated property, and we found no source explaining the 157.

GHRP, finally, is a descriptive class name with series numbers. In a 1998 paper, C. Y. Bowers calls the family “Growth hormone-releasing peptides”, and the numbers do not give residue counts: GHRP-2 and GHRP-6 are both six residues long.

Sequence names: when the name is the sequence

The third system needs no lookup, only the amino acid codes. Some names are a one-letter sequence written out, as GHK and KPV are. Others give a fragment of a parent protein by residue numbers: GHRH(1–29)NH2, a PubChem synonym for sermorelin, is the first 29 residues of growth hormone-releasing hormone with a C-terminal amide; Tyr-hGH177–191 is AOD9604; and ACTH(4–7)PGP, the name a 2020 paper uses for Semax, is residues 4–7 of ACTH followed by Pro-Gly-Pro.

A third pattern combines the first residues with the length. UniProt’s human cathelicidin entry lists LL-37, which begins Leu-Leu and is 37 residues long, alongside LL-29, LL-23, FF-33, RK-31, KS-30 and KR-20, all read the same way, and FALL-39, the 39-residue form that begins Phe-Ala-Leu-Leu. Kisspeptin-54, -14, -13 and -10 follow a simpler rule: the number is the length, counted back from the shared amidated C-terminus. Names like these can be decoded and checked directly against a stated sequence and a measured mass.

Same name, different molecule, and the reverse

Market names have no owner and no definition, so they drift, and TB-500 is a well-documented case. Thymosin beta-4 is a natural 43-residue peptide, but in 2012 anti-doping chemists at Ghent University reported finding “the N-terminal acetylated 17-23 fragment of human thymosin beta 4”, seven residues long, in a product sold as TB-500. The name is still attached to more than one molecule, so on its own it does not say which is meant. We found no primary source for who coined the name or what its number means; our sibling article on two unrelated peptides that share the thymosin name explains the family name itself.

CJC-1295 shows the same drift: the name appears both on the albumin-binding analogue it first described and, as “CJC-1295 without DAC”, on a different molecule. Even large databases slip: on 21 October 2026, the PubChem record for GHRP-6 (CID 4345065, C46H56N12O6) listed “GHRP-2 Acetate” among its depositor-supplied synonyms, though GHRP-2 is a different peptide, C45H55N9O6. The reverse also happens, with one molecule under several names: GHRP-2 and pralmorelin, or leuprorelin and leuprolide.

Modifiers in a product name deserve as much attention as the core. “No DAC”, “fragment”, “N-acetyl” and “amidate” each signal a different molecule from the parent, with its own formula and mass, and our catalogue lists such variants as separate products. Not every research peptide has an INN to fall back on, either: GHRP-2 has one, while the PubChem record for GHRP-6 lists none.

Checking the identity behind a name

Identity is settled by data that a name cannot carry. The table shows what each common identifier pins down and what it can miss.

IdentifierWhat it pins downWhat it can miss
Market or code nameWhich product a seller meansSequence, caps and salt; meaning can differ between sellers
INNOne substance, by WHO definitionThe salt form, and whether a vial matches
CAS Registry NumberOne registered substance, often form-specificSalt and peptide can differ: pralmorelin 158861-67-7, its dihydrochloride 158827-34-0
Sequence with caps and bridgesThe covalent structureStereochemistry, if D-residues are not marked
Molecular formulaComposition, including caps, bridges and any stated counter-ionIsomers: D- versus L-, leucine versus isoleucine
Monoisotopic massA measurable check on the formulaThe same isomers; deamidation versus a free C-terminal acid
Certificate for your batchWhat was measured in that batchAnything not tested, and other batches

Read the name, then the full sequence and formula, then check the certificate: any mass it reports should match the capped, bridged sequence, and its batch number should match your vial.

What’s established and what isn’t

Established, and citable

  • Each INN is unique, globally recognized and public property (WHO).
  • Stems define a pharmacologically related group (WHO stem book, 2018).
  • -morelin was redefined from “peptides” to “substances” in February 2026 (WHO addendum).
  • National names match INNs with rare exceptions (WHO, 2017), leuprolide being one (KEGG).
  • CJC-1295 was developed at ConjuChem, Montréal (Jetté and colleagues, 2005).
  • BPC 157 also appears as PL14736, PL-10, PLD-116 and Bepectin (Józwiak and colleagues, 2025).
  • A product sold as TB-500 contained an acetylated thymosin beta-4 fragment (Esposito and colleagues, 2012).

Open, or outside what a name can show

  • What the numbers in BPC 157, AOD9604, CJC-1295 and TB-500 mean; we found no primary source.
  • Whether AOD stands for anti-obesity drug; the developer-funded safety paper never expands it.
  • Who coined TB-500, and when.
  • Whether a market name means the same molecule from one supplier to the next.
  • Anything about effects: no name, stem or historical expansion is evidence of a biological property.

Searching for a compound in a Canadian catalogue

Our catalogue lists peptides under their research-market names — GHRP-2 rather than pralmorelin, Sermorelin rather than GHRH(1–29)NH2 — so search more than one way, on our site or anyone else’s, and apply the same checks to every supplier, including us.

  • Try the market name, the INN and any code, with and without hyphens or spaces: GHRP-2, GHRP 2, pralmorelin, KP-102.
  • Expect French forms. WHO’s cumulative INN list gives each name in Latin, English, French, Spanish, Arabic, Chinese and Russian, so a French-language Canadian source may use the French form of the same name.
  • When names disagree, compare sequences; a run of residues is harder to misattribute than a name.
  • Check that the listing gives a sequence, caps, formula and mass, and that the certificate matches them. If anything is missing, ask through our contact page before ordering.

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The names in our catalogue

BPC-157, TB-500, GHRP-6 and the -relin peptide ipamorelin are all in our catalogue. As this guide explains, a name is not proof, so check the Janoshik test report for each one on our Lab Testing page.

Research use only. Pure Peptides Canada products are laboratory reagents for in-vitro research, not for human or veterinary use. This article explains how peptide names arise, for education; it is not medical, dietary or dosing guidance, and it is not legal or regulatory advice.

Frequently asked questions

What does BPC stand for in BPC-157?

BPC is usually expanded as body protection compound. A 2025 literature and patent review describes BPC 157 as a 15-residue peptide isolated from human gastric juice and first described by Sikirić and colleagues in 1993. The name is historical and says nothing about what the peptide does, and we found no source that explains the number 157.

Why do peptide names end in -relin or -tide?

Because they are International Nonproprietary Names built from WHO stems. WHO defines -tide as peptides and glycopeptides and -relin as pituitary hormone-release stimulating peptides, while -morelin now covers growth hormone release-stimulating substances. A stem places a substance in a family of related substances but says nothing about its exact sequence.

What is an INN?

An International Nonproprietary Name is a generic name selected by the World Health Organization’s INN Programme. WHO describes each INN as a unique name that is globally recognized and is public property. Many research peptides are known only by code or market names, while some have both, such as GHRP-2, whose INN is pralmorelin.

Is TB-500 the same as thymosin beta-4?

Not reliably. Thymosin beta-4 is a natural 43-residue peptide, while TB-500 is a market name with no official definition. Ghent University anti-doping chemists reported in 2012 that a product sold as TB-500 contained an acetylated seven-residue fragment of thymosin beta-4. Only analysis of the vial, checked against a stated sequence, formula and mass, shows which molecule it contains.

What does GHRP stand for?

GHRP stands for growth hormone-releasing peptide, the term C. Y. Bowers uses for this family of synthetic peptides. The numbers do not give residue counts: GHRP-2 and GHRP-6 are both six residues long. GHRP-2 also has an INN, pralmorelin, and the development code KP-102.

Can two suppliers sell different molecules under the same name?

Yes. Market names have no official definition, so one name can be attached to different sequences, end caps or salt forms, and even database records can carry contradictory synonyms. Compare the full sequence, molecular formula and monoisotopic mass given for the product, and the certificate for your batch, rather than relying on the name, and ask the supplier when any of them is missing.

Look past the name

Check the sequence and certificate for anything you order. Browse the catalogue or see the Lab Testing page.

References

  1. World Health Organization. International Nonproprietary Names (INN). Health products policy and standards. World Health Organization
  2. World Health Organization. The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances. WHO/EMP/RHT/TSN/2018.1. Geneva, 2018. World Health Organization; and its cumulative addendum, INN Working Document 24.583, February 2024. World Health Organization
  3. World Health Organization. INN Stem Book Addendum 202602-2024 (INN Working Document 26.638), February 2026. World Health Organization
  4. World Health Organization. Pre-stems: suffixes used in the selection of INN, February 2026. World Health Organization
  5. World Health Organization. Guidance on the use of International Nonproprietary Names (INNs) for pharmaceutical substances. Geneva, 2017. World Health Organization
  6. Kanehisa Laboratories. KEGG DRUG entries D02040 (pralmorelin dihydrochloride), D08509 (sermorelin), D02117 (sermorelin acetate), D08113 (leuprolide; leuprorelin), D08027 (gonadorelin), D00176 (protirelin), D06404 (liraglutide), D06053 (teduglutide), D05594 (pramlintide), D12225 (mazdutide), D12898 (survodutide) and D12430 (retatrutide). KEGG
  7. National Center for Biotechnology Information. PubChem compound records for pralmorelin (synonyms GHRP-2 and KP-102; CAS 158861-67-7), sermorelin, ipamorelin and CID 4345065 (GHRP-6). PubChem
  8. Bowers CY. Growth hormone-releasing peptide (GHRP). Cellular and Molecular Life Sciences. 1998;54(12):1316–1329. doi:10.1007/s000180050257. Springer
  9. 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. doi:10.3390/ph18020185. MDPI
  10. Stier H, Vos E, Kenley D. Safety and tolerability of the hexadecapeptide AOD9604 in humans. Journal of Endocrinology and Metabolism. 2013;3(1-2):7–15. doi:10.4021/jem.v3i1-2.157. Journal of Endocrinology and Metabolism
  11. Teichman SL, Neale A, Lawrence B, Gagnon C, Castaigne JP, Frohman LA. 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. Journal of Clinical Endocrinology & Metabolism. 2006;91(3):799–805. doi:10.1210/jc.2005-1536. Oxford Academic
  12. Jetté L, Léger R, Thibaudeau K, et al. Human growth hormone-releasing factor (hGRF)1–29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology. 2005;146(7):3052–3058. doi:10.1210/en.2004-1286. Oxford Academic (DOI)
  13. Esposito S, Deventer K, Goeman J, Van der Eycken J, Van Eenoo P. Synthesis and characterization of the N-terminal acetylated 17–23 fragment of thymosin beta 4 identified in TB-500, a product suspected to possess doping potential. Drug Testing and Analysis. 2012;4(9):733–738. doi:10.1002/dta.1402. Wiley (DOI)
  14. UniProt Consortium. UniProtKB entries P49913 (cathelicidin antimicrobial peptide), Q15726 (KiSS-1) and P62328 (thymosin beta-4). UniProt
  15. Filippenkov IB, Stavchansky VV, Denisova AE, et al. Novel insights into the protective properties of ACTH(4-7)PGP (Semax) peptide at the transcriptome level following cerebral ischaemia–reperfusion in rats. Genes. 2020;11(6):681. doi:10.3390/genes11060681. MDPI

For laboratory research use only. Not for human or veterinary use. This article summarizes published nomenclature and scientific material for educational purposes and is not medical, legal or regulatory advice.