Research use only · Lyophilised material · Not a medicine · Not for human or veterinary use · Disclaimer

Sable · Reference

Dihexa: UK Research Peptide Reference

Verified reference data for research use only.

Research use only. Not for consumption. No health claims.

Last updated 2026-10-10

CAS Registry Number#
1401708-83-5Source · Verified 2026-10-10
Compound class#
peptidomimetic (angiotensin IV analogue)Source · Verified 2026-10-10
Molecular formula#
C27H44N4O5Source · Verified 2026-10-10
Molecular weight#
504.7 g/molSource · Verified 2026-10-10
Name#
DihexaSource · Verified 2026-10-10
PubChem CID#
129010512Source · Verified 2026-10-10
Storage (lyophilised)#
-20 °C, dry, protected from lightSource · Verified 2026-10-10
Synonyms#
N-hexanoic-Tyr-Ile-(6) aminohexanoic amide; PNB-0408Source · Verified 2026-10-10

Product page · Questions · JSON

Research questions

research_context

Dihexa mechanism of action?

In the research literature, Dihexa is described as an angiotensin IV-derived peptidomimetic studied for hepatocyte growth factor/c-Met interactions in neuroscience research models. It is classed as a peptidomimetic (angiotensin IV analogue). This describes its use as a laboratory research tool only, not any effect in people. Sable Peptides supplies it for laboratory research use only; it is not for human consumption.

Source: https://pubchem.ncbi.nlm.nih.gov/compound/129010512

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Cite this

Plain

Sable Peptides. (2026). Dihexa: UK Research Peptide Reference. UK Research Peptide Reference. Retrieved 2026-10-11, from https://www.sablepeptides.co.uk/ref/dihexa

APA

Sable Peptides. (2026, October 10). Dihexa: UK Research Peptide Reference. UK Research Peptide Reference. https://www.sablepeptides.co.uk/ref/dihexa

BibTeX

@misc{sable_dihexa_2026, author = {{Sable Peptides}}, title = {{Dihexa: UK Research Peptide Reference}}, year = {2026}, howpublished = {\url{https://www.sablepeptides.co.uk/ref/dihexa}}, note = {Accessed 2026-10-11. CC BY 4.0}}

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