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Compound monograph

Pralmorelin (GHRP-2)

Pralmorelin is a synthetic hexapeptide growth hormone secretagogue acting at the ghrelin receptor, containing three D-configured residues and a naphthylalanine substitution.

Published: 2026-09-13Literature/identifier verification: 2026-09-13
GHRP-2Growth hormone-releasing peptide-2KP-102Growth hormone secretagogues

01

Identity & nomenclature

Pralmorelin is a synthetic hexapeptide growth hormone secretagogue acting at the ghrelin receptor, containing three D-configured residues and a naphthylalanine substitution.

GHRP-2 is not GHRP-6; they are different hexapeptides. And GHRP does not denote a GHRH-receptor ligand — the similar names refer to GH secretion, not a shared receptor. A generic 'Nal' field loses both the 2-naphthyl substitution and the D configuration, either of which changes the molecule.

Declared aliases and development codes: GHRP-2, Growth hormone-releasing peptide-2, KP-102.

02

Molecular properties

Molecular formulaC45H55N9O6
Molecular mass817.99 Da
CAS Registry Number158861-67-7
PubChem CID6918245
UNIIE6S6E1F19M
Three-letter sequenceD-Ala–D-2-Nal–Ala–Trp–D-Phe–Lys–NH2

No one-letter string is published here. Position 2 is 3-(naphthalen-2-yl)-D-alanine, a single nonstandard residue; written as ordinary letters it would denote different amino acids. Three of six residues are D-configured and the stereochemistry is identity-defining, not annotation.

03

Structural characteristics

Pituitary work distinguishes its direct action from GHRH-mediated responses, and it appears in CD36 binding competition experiments alongside hexarelin. The CD36 observation is a binding result in the systems tested; it does not establish that every pralmorelin response is CD36-mediated.

  • D-2-naphthylalanine at position 2
  • D-Ala1
  • D-Phe5

Terminal features: Free N-terminus, C-terminal amide at Lys6.

04

Molecular targets & mechanisms

05

Analytical considerations

An intact-mass match distinguishes neither D from L residues nor 1-naphthyl from 2-naphthyl positional isomers — both are identical in elemental composition. Those require chiral amino-acid analysis with authentic standards, or NMR. A growth-hormone secretion assay cannot establish which GHRP is present; the comparative LC-MS work is the reference that actually separates them.

06

Verified bibliography

  1. Identification of the growth hormone-releasing peptide binding site in CD36: a photoaffinity cross-linking study.

    Demers A, McNicoll N, Febbraio M, Servant M, Marleau S, Silverstein R, Ong H

    The Biochemical journal · 2004-09-01 · Journal Article

    current
  2. Determination of growth hormone releasing peptides (GHRP) and their major metabolites in human urine for doping controls by means of liquid chromatography mass spectrometry.

    Thomas A, Höppner S, Geyer H, Schänzer W, Petrou M, Kwiatkowska D, Pokrywka A, Thevis M

    Analytical and bioanalytical chemistry · 2011-02-06 · Journal Article

    current

10

Methodology & citation verification

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