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NORTHVERITY / HX5

Hexarelin Acetate

5 mg × 10 vials

For laboratory procurement

Hexarelin Acetate 5 mg × 10 vials · HX5 · Catalog illustration—not an actual packaging photo.
Catalog illustration—not an actual packaging photo.
Procurement details
Catalog number
HX5
Listed specification
5 mg
Vials per pack
10 vials
Current supply lot
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Compound profile

Hexarelin is an amidated synthetic hexapeptide containing D-2-methyltryptophan, examined in CD36 binding studies.

Identity

Sequence
H-H[D-Trp(2-Me)]AW[D-Phe]K-NH2
Residues
6
Molecular formula
C47H58N12O6
Average molecular weight
887 g/mol
Monoisotopic mass (calculated)
886.4602 Da
CAS number
140703-51-1
PubChem CID
6918297
Other names
Examorelin

Values describe the free peptide without the catalog’s acetate counterion. Residue 2 is D-2-methyltryptophan, represented schematically. No separate UniProt identity was verified; the profile uses a residue diagram without SMILES, atomic coordinates or blend components.

Identity data from: PubChem CID 6918297

Residue diagram of Hexarelin
Drawn from the verified identity data on this page.

Research overview

Hexarelin, also called examorelin, is a synthetic peptide of six amino acid residues. Its amidated sequence contains D-2-methyltryptophan at position 2 and D-phenylalanine at position 5. The methyl substitution distinguishes it from GHRP-6. Although grouped with growth hormone releasing peptides, hexarelin has also been examined as a ligand for CD36, a membrane scavenger receptor. This additional binding context is explicitly addressed in studies of cardiac membranes and receptor-expressing cells [1][2].

A photoaffinity cross-linking study used a labelled hexarelin derivative to locate the interacting region of CD36. Experiments with rat cardiac membranes and cells expressing human CD36 mapped the binding site to a receptor segment spanning Asn132 to Glu177, with Met169 identified within the labelled region. These residue numbers belong to CD36, not to the six-residue peptide. The work concerns ligand contact and receptor structure rather than a general assignment of peptide activity across all tissues [1].

An earlier investigation identified CD36 as a hexarelin-binding protein in cardiac membranes and examined receptor involvement in isolated perfused hearts. Models with CD36 deficiency or deletion helped distinguish receptor-dependent responses. Together, the studies provide a defined molecular and experimental context for hexarelin: binding-site mapping and receptor-dependence are complementary questions, and neither alone establishes that other short secretagogue peptides share the same interaction [2].

Laboratory storage and handling

Store sealed peptide vials under the temperature conditions stated in the lot documentation, protected from light and moisture. Let a cold vial reach room temperature before opening to limit condensation. Avoid repeated freezing and thawing of laboratory stocks, record storage history and the lot identifier, and use standard laboratory protective equipment. Chemical modifications and counterions should be checked against the supplied analytical description.

Questions about Hexarelin

What distinguishes hexarelin from GHRP-6?

Hexarelin contains a methyl substituent on the D-tryptophan at residue 2. Retaining that substitution is necessary for its molecular identity and its residue diagram.

What was mapped in the CD36 study?

Photoaffinity cross-linking located a hexarelin-binding region within CD36. The receptor residues Asn132, Glu177 and Met169 describe CD36 positions rather than peptide positions [1].

Which models examined receptor dependence?

The earlier study used cardiac membranes and isolated perfused hearts, including models deficient in CD36. Those preparations addressed receptor involvement in the measured response [2].

References

  1. Identification of the growth hormone-releasing peptide binding site in CD36: a photoaffinity cross-linking study. Biochem J 2004. PMID 15176951
  2. CD36 mediates the cardiovascular action of growth hormone-releasing peptides in the heart. Circ Res 2002. PMID 11988484

Identity data checked on 2026-10-03. Literature summaries describe published research models and are not specifications of any product lot.

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