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Gray-Market Name Decoder

GLP-3, GLP-2, KLOW, Wolverine, PDA: the names on gray-market peptide vials often hide the molecule inside. This page decodes 14 of them, with the molecule each one points to, its approval and anti-doping status, the identity risks, and the questions that establish what is actually in a vial. Every name has one source, and no seller is named.

GLP-3

Nickname

Also: Reta, Triple-G

What it refers to: Retatrutide, one peptide that activates three receptors: GLP-1, GIP and glucagon. There is no hormone called GLP-3; the name counts receptors.

  • Retatrutide Clinical Trials WADA 2026: not named; falls under S0, unapproved substances

Identity risks

  • Retatrutide is investigational and approved nowhere; the FDA says it cannot be used in compounding.
  • A vial sold under any of these names may not contain retatrutide, or the amount on the label.

Questions to ask

  • Is this retatrutide, by name, and how many milligrams?
  • Is there a lab report for this batch that identifies the molecule by mass?

Source (News report): BBC Science Focus, “A really substantive jump”: the most powerful weight-loss drug ever tested has arrived, which calls retatrutide “otherwise known as ‘triple-G’, ‘GLP-3’ or ‘reta’” (read October 1, 2026). Source

GLP-1-R

Seller label

Also: GLP-1-R peptide

What it refers to: Retatrutide, labelled with a name that reads like a GLP-1 drug.

  • Retatrutide Clinical Trials WADA 2026: not named; falls under S0, unapproved substances

Identity risks

  • “GLP-1R” is the standard abbreviation for the GLP-1 receptor, so the label suggests a single GLP-1 agonist when the molecule is a triple agonist.
  • The FDA found this label on a product marketed for research but intended, it said, for human use.

Questions to ask

  • Which molecule is it: retatrutide, or a GLP-1 agonist such as semaglutide?
  • Does the lab report name the molecule, not the label?

Source (FDA): US FDA warning letter MARCS-CMS 721806, March 31, 2026, to an online seller: retatrutide “also referred to by your firm as ‘GLP-1-R peptide’” (read October 1, 2026).

GLP-2

Seller label

Also: GLP-2 peptide

What it refers to: Tirzepatide, a GIP and GLP-1 receptor agonist, labelled with the name of a different hormone.

Identity risks

  • GLP-2 is a real, separate gut hormone, and teduglutide, a GLP-2 analogue, is an approved drug for short bowel syndrome, so the label can point to the wrong molecule in either direction.
  • Tirzepatide is approved only as Mounjaro and Zepbound; a vial labelled GLP-2 is neither.

Questions to ask

  • Is it tirzepatide or actual GLP-2?
  • How many milligrams, and is there a lab report naming the molecule?

Not to be confused with: GLP-2, Teduglutide

Source (FDA): US FDA warning letter MARCS-CMS 721806, March 31, 2026, to an online seller: tirzepatide “also referred to by your firm as ‘GLP-2 peptide’” (read October 1, 2026).

GLP-2T

Seller label

Also: GLP-2 T, GLP-2 (TZ), GLP-2 (Tirz)

What it refers to: Tirzepatide, with a letter added to the GLP-2 label to hint at the molecule.

Identity risks

  • The same collision as GLP-2: the name of a real hormone on a different drug.
  • Listings describe the contents as tirzepatide but sell it as research material, outside any approval.

Questions to ask

  • Does the listing name tirzepatide outright, and at what amount?
  • Is the lab report for this batch, not a generic sample?

Source (Our listing review): Grey Peptides listing review, October 1, 2026: listings for “GLP-2 T” and “GLP 2 (TZ)” describe the contents as tirzepatide. Sellers are not named.

Wolverine

Blend

Also: Wolverine stack, Wolverine blend

What it refers to: Usually BPC-157 and TB-500 together, often 10 mg of each. The name is also used for BPC-157 alone and for the four-peptide KLOW mix.

  • BPC-157 Research Only WADA 2026: prohibited (S0)
  • TB-500 Research Only WADA 2026: prohibited (S2.3)

Identity risks

  • Neither component is FDA-approved, and WADA names both on its Prohibited List.
  • The name does not fix the contents: three different products answer to it.

Questions to ask

  • Which peptides, and how many milligrams of each?
  • Is TB-500 the short fragment or the full thymosin beta-4 protein?

Source (News report): Forbes Health, The FDA Eased Restrictions On Six Peptides: What Consumers Should Know, describing the “Wolverine Stack” as a combination of TB-500 and BPC-157 (read October 1, 2026). Source

KLOW

Blend

Also: KLOW blend

What it refers to: Usually GHK-Cu 50 mg, BPC-157 10 mg, TB-500 10 mg and KPV 10 mg in one 80 mg vial. At least one listing reverses the GHK-Cu and BPC-157 amounts.

  • GHK-Cu Research Only WADA 2026: not named; falls under S0, unapproved substances
  • BPC-157 Research Only WADA 2026: prohibited (S0)
  • TB-500 Research Only WADA 2026: prohibited (S2.3)
  • KPV Research Only WADA 2026: not named; falls under S0, unapproved substances

Identity risks

  • No published study has tested this mix, and none of its four components is FDA-approved.
  • Five times more GHK-Cu than anything else means a dose chosen for one component fixes the others.

Questions to ask

  • What are the milligrams of each of the four?
  • Does the lab report quantify all four, or only one?

Source (Our listing review): Grey Peptides listing review, September 26, 2026, in KLOW vs GLOW vs Wolverine: the compositions stated on the listings read. Sellers are not named. Read it

GLOW

Blend

Also: GLOW blend

What it refers to: GHK-Cu 50 mg, BPC-157 10 mg and TB-500 10 mg in one 70 mg vial: KLOW without the KPV.

  • GHK-Cu Research Only WADA 2026: not named; falls under S0, unapproved substances
  • BPC-157 Research Only WADA 2026: prohibited (S0)
  • TB-500 Research Only WADA 2026: prohibited (S2.3)

Identity risks

  • No published study has tested this mix, and none of its components is FDA-approved.
  • BPC-157 and TB-500 are on WADA's Prohibited List.

Questions to ask

  • What are the milligrams of each?
  • Does the lab report quantify all three?

Source (Our listing review): Grey Peptides listing review, September 26, 2026, in KLOW vs GLOW vs Wolverine: the listings read agreed on this composition. Sellers are not named. Read it

Tri-Heal

Blend

Also: Tri-Heal Max

What it refers to: TB-500 25 mg, BPC-157 10 mg and KPV 10 mg in one 45 mg vial.

  • TB-500 Research Only WADA 2026: prohibited (S2.3)
  • BPC-157 Research Only WADA 2026: prohibited (S0)
  • KPV Research Only WADA 2026: not named; falls under S0, unapproved substances

Identity risks

  • No published study has tested this mix, and none of its components is FDA-approved.
  • It overlaps with Wolverine and KLOW, so combining them doubles up the same peptides.

Questions to ask

  • What are the milligrams of each of the three?
  • Does the lab report quantify all three?

Source (Our listing review): Grey Peptides listing review, October 1, 2026: two listings for Tri-Heal Max state TB-500 25 mg, BPC-157 10 mg and KPV 10 mg. Sellers are not named.

PDA

Rebrand

Also: Pentadeca arginate, BPC-157 arginate

What it refers to: Described as BPC-157's own 15-amino-acid sequence prepared as an arginine salt instead of the usual acetate.

  • BPC-157 Research Only WADA 2026: prohibited (S0)

Identity risks

  • PubMed holds no study of “pentadeca arginate”; everything claimed for it comes from BPC-157 research.
  • A salt form changes how a powder is handled, not the peptide's sequence, so it inherits BPC-157's status.

Questions to ask

  • Is this BPC-157 under another name?
  • What is the stated sequence, and what does the lab report show?

Source (Our listing review): Grey Peptides review, October 1, 2026: pages selling or describing PDA call it BPC-157's sequence as an arginate salt, and a PubMed search for “pentadeca arginate” returns no records. Sellers are not named.

TB-500

Code name

Also: TB500, TB-4 fragment

What it refers to: A derivative of thymosin beta-4, sold as a short synthetic fragment rather than the full protein.

  • TB-500 Research Only WADA 2026: prohibited (S2.3)
  • Thymosin β4 Clinical Trials WADA 2026: prohibited (S2.3)

Identity risks

  • The fragment has never been tested in people; the research behind it is mostly on the full protein.
  • WADA names it under S2.3, among thymosin beta-4 derivatives.

Questions to ask

  • Is it the fragment or the full thymosin beta-4 protein?
  • What sequence and mass does the lab report show?

Source (WADA): WADA 2026 Prohibited List, section S2.3: “Thymosin-ß4 and its derivatives e.g. TB-500” (read October 1, 2026). Source

MT-II

Code name

Also: MT2, Melanotan 2

What it refers to: Melanotan II, an unselective melanocortin receptor agonist sold for tanning.

  • Melanotan II Research Only WADA 2026: not named; falls under S0, unapproved substances

Identity risks

  • It was never developed into an approved product.
  • It is easy to confuse with afamelanotide, a different melanocortin drug approved as the Scenesse implant for a light-sensitivity disorder.

Questions to ask

  • Is it melanotan II, and how many milligrams per vial?
  • Is there a lab report for this batch?

Not to be confused with: Afamelanotide

Source (PubMed): A 2005 study names “melanotan-II (MT-II)” in its title (PMID 15967265). PubMed

PT-141

Code name

Also: PT141

What it refers to: Bremelanotide, the melanocortin agonist approved as Vyleesi for low sexual desire in premenopausal women.

  • PT-141 FDA Approved WADA 2026: not on the List

Identity risks

  • The approved drug is a prescription injection for premenopausal women; vials sold as PT-141 are research material outside that approval.
  • Nausea affected about 40% in the phase 3 trials.

Questions to ask

  • Is it bremelanotide, and at what dose per vial?
  • Is it a pharmacy-dispensed product or research material?

Source (PubMed): A 2006 trial names its drug as “bremelanotide (PT-141)” (PMID 16839319). PubMed

SS-31

Code name

Also: MTP-131, Bendavia

What it refers to: Elamipretide, approved in 2025 as Forzinity for muscle strength in Barth syndrome.

Identity risks

  • The approval covers one rare disease; trials in mitochondrial myopathy and heart failure found no benefit.
  • Vials sold as SS-31 are research material outside that approval.

Questions to ask

  • Is it elamipretide, and how many milligrams?
  • Is there a lab report for this batch?

Source (PubMed): A 2025 review gives the names as “Elamipretide (SS-31, MTP-131, Bendavia)” (PMID 39940712). PubMed

CJC-1295 without DAC

Code name

Also: CJC no DAC

What it refers to: A GHRH(1-29) analogue sold without the albumin-binding group, the DAC, that defines CJC-1295 in its published research.

  • CJC-1295 Discontinued WADA 2026: prohibited (S2.2.4)
  • Sermorelin Discontinued WADA 2026: prohibited (S2.2.4)

Identity risks

  • The published CJC-1295 trials tested the version with DAC; without it the half-life and effects are not those trials'.
  • WADA names CJC-1295 on its Prohibited List, under S2.2.4.

Questions to ask

  • With DAC or without?
  • What sequence does the lab report show?

Source (PubMed): A 2026 review lists “CJC-1295 with Drug Affinity Complex [DAC]” and “CJC-1295 without DAC” among peptides marketed as research compounds (PMID 42395176). PubMed

Why the nicknames exist

Most of the peptides sold online are sold as research chemicals, with a label saying they are not for human use. A seller who names an approved drug, or a drug still in trials, invites the attention of regulators; a nickname is softer. Some names began as shorthand on forums and stuck, some were coined by sellers, and some were picked up by the press. Whatever their origin, they now stand between a buyer and the molecule in the vial.

The FDA's position is that the label does not decide what a product is. In its statement on unapproved GLP-1 drugs, it says it has warned companies selling semaglutide, tirzepatide, retatrutide, survodutide and mazdutide labelled “for research purposes” or “not for human consumption” while selling them to consumers with dosing instructions, and that retatrutide and cagrilintide cannot be used in compounding at all (FDA). Its warning letters quote the labels sellers use, which is how one of them records a firm calling retatrutide “GLP-1-R peptide” and tirzepatide “GLP-2 peptide”.

Three ways a nickname misleads

It borrows the name of a different molecule. GLP-2 is a real hormone with a real drug based on it, teduglutide, approved for short bowel syndrome. A vial labelled GLP-2 that contains tirzepatide sends the reader to the wrong page of the textbook, and a reader looking for actual GLP-2 can end up with a weight-loss drug. GLP-1R is the standard abbreviation for the GLP-1 receptor; on a label it suggests a single GLP-1 agonist, not a triple one. GLP-3 sounds like a hormone and is not one: it counts receptors, one, two and three, a numbering with no standing in endocrinology.

It hides the amounts. A blend name says which peptides are in the vial, sometimes, but not how much of each. KLOW is usually 50 mg of GHK-Cu with 10 mg each of BPC-157, TB-500 and KPV, but at least one listing reverses the first two amounts, and in an 80 mg vial that is a fivefold difference in the dose of each. Because the ratio is fixed, a dose chosen for one component decides the dose of the others.

It means different things to different sellers. Wolverine usually means BPC-157 with TB-500, but it is also used for BPC-157 alone and for the four-peptide KLOW mix. A forum post that says “Wolverine” cannot tell you which was meant, and neither can a label that uses the name without amounts.

What a blend name does to a dose

Blend names deserve their own warning, because the arithmetic is unforgiving. In the usual KLOW vial, 50 of the 80 milligrams are GHK-Cu, so 62.5% of every dose drawn from it is GHK-Cu and 12.5% is each of the other three. Someone aiming for 250 micrograms of BPC-157 from that vial is drawing 2 milligrams of blend, and with it 1.25 milligrams of GHK-Cu. If the listing that reverses the first two amounts is the one in hand, the same draw delivers 1.25 milligrams of BPC-157 instead, five times the intended amount. The name on the vial is identical in both cases. Our blend calculator does this arithmetic for any stated composition, which is only as good as the composition the label states.

When the code name belongs to a real drug

Some names on this page are not slang at all. PT-141, SS-31 and MT-II were the laboratory code names of molecules that went on to be studied under their own names, and two of them, bremelanotide and elamipretide, are now FDA-approved drugs. That makes the research vial more confusing, not less: the approval covers a specific product, made to drug manufacturing standards, for a specific use, at a specific dose. A vial sold under the code name shares the molecule's name and nothing else, and the evidence for the approved drug says nothing about what the vial contains.

The opposite case matters too. Retatrutide has strong trial results and no approval, so a nickname that makes it sound like a newer GLP-1 drug borrows a credibility it has not yet earned. According to the FDA, it has not been found safe and effective for any condition, and it cannot be used in compounding under federal law.

What athletes should know

The anti-doping question is separate from the medical one. WADA's Prohibited List names some of these peptides outright: BPC-157 under S0, TB-500 among the thymosin beta-4 derivatives under S2.3, and CJC-1295 under S2.2.4. Peptides the List does not name are not automatically allowed: its S0 section covers substances with no current approval for human therapeutic use by any government health authority, which is where retatrutide, GHK-Cu, KPV and melanotan II sit, according to our reading of the 2026 List. A nickname is not a defence, because testing looks for the molecule, not the label.

How to decode a name

Start with the international nonproprietary name, the INN: retatrutide, tirzepatide, bremelanotide, elamipretide. Code names such as PT-141 and SS-31 were the development names of molecules that later received INNs, and in two of those cases an approved drug now exists, which makes the difference between the drug and a research vial sharper, not softer. If a seller will not name the molecule, that is the answer.

Then ask for amounts in milligrams, per molecule, and a lab report for the batch you would actually receive. A certificate of analysis that identifies the molecule by its mass, rather than by the seller's own name for it, is the only document in the chain that can settle identity; our COA decoder explains what a credible one contains. For blends, the report should quantify every component, not only the first.

Finally, look the molecule up rather than the nickname. Each card above links to the encyclopedia entry for every molecule a name points to, with its regulatory status and its standing on the World Anti-Doping Agency's 2026 Prohibited List. Athletes in tested sport should know that several of these names, among them TB-500, BPC-157 and CJC-1295, appear on that List by name, and that substances it does not name may still fall under its S0 category for unapproved substances.

How this page is sourced

Every mapping names exactly one source. Where a regulator, a journal or a news report has recorded the name, that is the source: an FDA warning letter, the WADA List, a PubMed record, or a named publication. Where only sellers use a name, the source is our own listing review, dated, and the composition is the one the listings state. We do not name or link to sellers anywhere on this site, so FDA warning letters are cited by their MARCS-CMS number and date, which is enough to find them in the FDA's own database.

A name on this page is a claim about what sellers mean, not a statement about what any particular vial contains. Research-grade products are made outside drug manufacturing standards. When vials sold online as 10 mg of melanotan II were tested, they held between 4.3 and 8.8 mg, and some carried unknown impurities (see the melanotan II entry). Even when the nickname and the molecule match, the contents still have to be shown. Our article on where gray-market peptides come from covers that side of the problem.

Names change quickly. If you meet a nickname that is not here, the same three questions apply: which molecule, how much of it, and what does the batch report show.

This page describes how products are named and sold; it is not medical advice and not a buying guide. Nothing here is a recommendation to use any of these substances.