15% OFF $150+· CodeFALL15
Ends October 15Shop now
Lot certificates published
Plain, secure packaging

parent and analog

GHK (Prezatide) vs Pal-GHK (Palmitoyl Tripeptide-1)

Pal-GHK is the N-palmitoylated derivative of the GHK tripeptide. Covalent acylation distinguishes it from free GHK.

Published: 2026-10-03Library record comparison: 2026-10-03

01

Identity side by side

Recorded molecular identities of GHK (Prezatide) and Pal-GHK (Palmitoyl Tripeptide-1)
Recorded fieldGHK (Prezatide)Pal-GHK (Palmitoyl Tripeptide-1)
Canonical namePrezatidePalmitoyl tripeptide-1
AliasesGHK; Glycyl-L-histidyl-L-lysine; Tripeptide-1Pal-GHK; N-palmitoyl-GHK; C16-GHK; Palmitoyl oligopeptide
Development codesNSC-379527not recorded
CAS49557-75-7147732-56-7
UNII39TG2H631ERV743D216M
PubChem CID7358710231864
Molecular formulaC14H24N6O4C30H54N6O5
Molecular weight (Da)340.38578.8
Sequence length (residues)33
Terminal modificationsnot recordedN-terminal palmitoylation
Structural modificationsnot recordednot recorded

GHK (Prezatide): nomenclature notes

GHK, GHK-Cu and Pal-GHK are three different substances: an uncomplexed peptide, a copper coordination species, and a covalently lipidated derivative. CAS 49557-75-7 belongs to THIS entry, the free tripeptide. The copper complex is 89030-95-5. That distinction has practical consequences — certificates of analysis in this market have carried the free-tripeptide number on copper-complex product, which describes the wrong substance.

Pal-GHK (Palmitoyl Tripeptide-1): nomenclature notes

'Palmitoyl oligopeptide' is not a unique identifier and should be kept only as a qualified alias; it is used for other lipidated peptides too. Pal-GHK is also not GHK-Cu with a delivery modification bolted on: acylating the N-terminal amine alters a group that participates in GHK's copper coordination, so copper behaviour must be measured for this molecule rather than inherited from the free ligand.

02

Recorded modification details

An aligned one-letter sequence is not recorded for this pair. The stored modification and sequence notes are shown below.

GHK (Prezatide)

Terminal modifications
not recorded
Structural modifications
not recorded
Stored three-letter notation
Gly · His · Lys · OH
Sequence notes
Three residues with a free N-terminal amine and a free C-terminal carboxyl. No modifications. Copper is NOT part of this entry — see nomenclatureNotes.

Pal-GHK (Palmitoyl Tripeptide-1)

Terminal modifications
N-terminal palmitoylation
Structural modifications
not recorded
Stored three-letter notation
Pal · Gly · His · Lys · OH
Sequence notes
The GHK tripeptide with a hexadecanoyl (palmitoyl) cap on the glycine alpha-amino group. 'Pal' is the acyl cap, not an amino-acid token. The lysine side-chain amine and the C-terminal carboxyl remain free. No copper is part of this identity.

03

Recorded mechanisms

These lists show the links recorded in each monograph. An unlisted link does not establish its absence from the molecule’s biology.

Shared recorded links

not recorded

Recorded only for GHK (Prezatide)

not recorded

Recorded only for Pal-GHK (Palmitoyl Tripeptide-1)

not recorded

04

Recorded compound classes

Shared recorded links

Recorded only for GHK (Prezatide)

Recorded only for Pal-GHK (Palmitoyl Tripeptide-1)

not recorded

05

References for the relationship

  1. Development of a LC-MS/MS method to monitor palmitoyl peptides content in anti-wrinkle cosmetics.

    Chirita RI, Chaimbault P, Archambault JC, Robert I, Elfakir C

    Analytica chimica acta · 2009-03-20 · Journal Article

    current
  2. SPARC is a source of copper-binding peptides that stimulate angiogenesis.

    Lane TF, Iruela-Arispe ML, Johnson RS, Sage EH

    The Journal of cell biology · 1994-05 · Journal Article

    current

06

Read the full monographs