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For research use only — not for human consumption
Vasonatrin original Regena research vial

Cardiovascular · Synthetic chimeric natriuretic peptide

Vasonatrin

Also known as Vasonatrin peptide; VNP

A synthetic 27-residue chimera combining CNP-22 with the ANP C-terminal pentapeptide for natriuretic peptide receptor research.

Length
27 amino acids
Half-life
Not well characterised
Mechanism
Vasonatrin produces natriuretic peptide-like, cGMP-associated signalling through membrane guanylyl cyclase receptor pathways. Its CNP-derived structure supports investigation of NPR-B-associated activity, but exclusive receptor selectivity should not be assumed without direct comparison against NPR-A.
Studied in
Cultured vascular cells, isolated arteries and veins, and animal cardiovascular and renal models are used to investigate vasonatrin-associated cGMP signalling and vascular reactivity.

About Vasonatrin

Vasonatrin is a synthetic chimera described in the early 1990s, rather than a peptide isolated as an endogenous precursor product. Its design joins the complete 22-residue C-type natriuretic peptide sequence to the five-residue C-terminal segment of atrial natriuretic peptide. This produces a 27-residue molecule with a disulphide-constrained ring and an added tail. The appended ANP-derived sequence is NSFRY, providing a defined structural change for comparisons with unmodified CNP-22 in receptor and tissue assays.

The original research rationale was to explore whether adding an ANP-derived tail would alter the experimental profile of the CNP scaffold. Studies have examined cGMP generation, vascular smooth-muscle responses and renal physiology in laboratory models. These readouts do not, by themselves, identify a single receptor subtype. Because natriuretic peptide receptors differ across tissues, mechanistic work should compare NPR-A and NPR-B directly and distinguish signalling receptor activity from binding or clearance mediated by NPR-C.

Laboratory notes

  • Confirm that the material is the CNP-22–NSFRY chimera; similarly described natriuretic peptide constructs may have different sequences.
  • Verify disulphide formation and compare activity with a matched CNP-22 reference.
  • Use separate NPR-A and NPR-B expression systems for receptor assignment rather than inferring selectivity from tissue cGMP alone.

Storage and reconstitution basics: storage guide.

Questions about Vasonatrin

Is vasonatrin a naturally occurring peptide?

It was designed as a synthetic chimera combining structural elements from CNP and ANP.

Which part of ANP is included?

The C-terminal pentapeptide NSFRY is appended to the full CNP-22 sequence.

Does a cGMP response prove NPR-B selectivity?

No. Both NPR-A and NPR-B generate cGMP, so receptor-defined assays are needed to distinguish their contributions.

Is Vasonatrin for human use?

No. It is supplied strictly for in-vitro laboratory research and is not for human or animal consumption.

Related research peptides

All products are sold for laboratory research use only. Not for human consumption, not a medicine, not for diagnosing, treating or preventing any condition.