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Relaxin: The Two-Chain Pregnancy Hormone — and Why Its Drug Version Failed in Heart Failure

Relaxin is a hormone of two short peptide chains, 24 and 29 amino acids long, held together by disulfide bonds. Best known for loosening ligaments and softening the cervix in pregnancy, it was developed as a heart-failure drug, serelaxin, which missed its endpoints in a 6,545-patient trial in 2019. No relaxin medicine is approved.

Made by the bodyTwo chains: 24 + 29 amino acidsNo FDA-approved product (openFDA, 2026-10-03)

Caroline S · Published 2026-10-03

Length

53 amino acids in two chains — an A chain of 24 and a B chain of 29 — joined by two disulfide bonds, with a third inside the A chain

Sequence

A chain QLYSALANKCCHVGCTKRSLARFC (residues 162–185); B chain DSWMEEVIKLCGRELVRAQIAICGMSTWS (residues 25–53) of the 185-residue human prorelaxin H2 precursor (UniProt P04090)

Origin

Made in the body as a single precursor chain (prorelaxin) from which a long connecting peptide is cut out, leaving two chains bridged by sulfur bonds — the same architecture as insulin. Humans carry three relaxin genes (RLN1, RLN2, RLN3); relaxin-2 is the form studied as a drug.

Last reviewed

2026-10-03

What is it good for?

In the body, pregnancy: UniProt's annotation describes it acting with oestrogen to widen the birth canal and remodel connective tissue — growth of the pubic ligaments and ripening of the cervix. As a medicine, nothing yet: its recombinant form, serelaxin, failed its phase 3 heart-failure trial in 2019.

Illustration: Two intertwined white molecular peptide chains with copper bonds on a white lab bench.
Illustration

What it is

Relaxin is a hormone made of two peptide chains, built the same way as insulin. UniProt's record for human prorelaxin H2 (P04090) — the form called relaxin-2 — gives the structure:

  • an A chain of 24 amino acids: QLYSALANKCCHVGCTKRSLARFC;
  • a B chain of 29 amino acids: DSWMEEVIKLCGRELVRAQIAICGMSTWS;
  • two disulfide bonds — bridges between sulfur atoms — tying the chains together, and a third inside the A chain.

Both chains come from one 185-residue precursor. The cell makes the whole chain, folds it, and then cuts out a 102-residue connecting peptide, leaving the two halves bolted together. Insulin does exactly this, with C-peptide as its cut-out piece.

Humans carry three relaxin genes. Relaxin-1 and relaxin-2 share the pregnancy annotation in UniProt; relaxin-3 is annotated as a brain neuropeptide acting on different receptors (RXFP3 and RXFP4).

What it does

UniProt's function annotation describes relaxin as an ovarian hormone that acts with oestrogen to widen the birth canal in many mammals, and as possibly involved in remodelling connective tissue in pregnancy — growth of the pubic ligaments and ripening of the cervix. It acts through RXFP1 (UniProt Q9HBX9), a receptor that raises cyclic AMP inside the cell.

What is described How firm
Birth-canal widening with oestrogen Described across many mammals
Connective-tissue remodelling in human pregnancy UniProt: "may be involved"
Anti-scarring effects in heart, lung, kidney Animal models (see B7-33)

The drug that did not work

Relaxin's anti-scarring effects in animal models made it a heart-failure candidate. Its recombinant form, serelaxin, went into RELAX-AHF-2: 6,545 people hospitalised with acute heart failure (New England Journal of Medicine, 2019, PMID 31433919).

Outcome at day 180 Serelaxin Placebo
Cardiovascular death 8.7% 8.9%
Worsening heart failure not significantly reduced —

That is the largest human result in the relaxin family, and it is negative for that use. It does not say anything about relaxin in pregnancy, where the hormone is the body's own.

Where it stands

openFDA's Drugs@FDA returns no application for relaxin or serelaxin (2026-10-03). PubMed returns 3,982 records for relaxin, 75 tagged as randomised controlled trials. The research-market fragment B7-33 is cut from its B chain and has no human trials.

Relaxin's two-chain build is shared with insulin, whose cut-out piece is recorded in C-peptide. For hormones that act during pregnancy and birth, see the labour hormone oxytocin; for peptides discussed for joint and ligament tissue, see peptides for joints and tendons.

What the research shows

Remodels connective tissue in pregnancy

UniProt P04090 function annotation (described across many mammals; 'may be involved' in human pregnancy remodelling)

Improves outcomes in acute heart failure

No. Serelaxin vs placebo in 6,545 patients: cardiovascular death at 180 days 8.7% vs 8.9%; worsening heart failure not significantly reduced (N Engl J Med 2019, PMID 31433919)

Is available as an approved US medicine

No. openFDA's Drugs@FDA returns no application for relaxin or serelaxin (2026-10-03)

Bars show how much of the evidence is in humans, not how well anything works.

Where it stands

In the body

An ovarian hormone (UniProt P04090), acting through the relaxin receptor RXFP1.

United States

No FDA application lists relaxin or serelaxin (openFDA, 2026-10-03).

Published record

PubMed returns 3,982 records for relaxin, 75 tagged as randomised controlled trials (2026-10-03).

Frequently asked questions

What is relaxin?

A hormone made of two short peptide chains — 24 and 29 amino acids — held together by disulfide bonds. UniProt annotates it as an ovarian hormone, and it is best known for its role in pregnancy, where it helps remodel connective tissue.

What does relaxin do in pregnancy?

UniProt's annotation, summarising the literature across many mammals, describes it acting with oestrogen to widen the birth canal, promote growth of the pubic ligaments and ripen the cervix. How much of that is established in humans specifically is less settled; the annotation itself uses 'may be involved'.

Is relaxin related to insulin?

Structurally, yes. Both are made as one precursor chain from which a connecting peptide is cut out, leaving two chains bridged by sulfur bonds. They act on different receptors and do different jobs.

Is there a relaxin drug?

Not an approved one. Serelaxin, a recombinant copy of relaxin-2, was tested in 6,545 people with acute heart failure; cardiovascular death at 180 days was 8.7% on serelaxin and 8.9% on placebo (NEJM 2019). openFDA lists no relaxin application (2026-10-03).

What is B7-33?

A short synthetic piece of relaxin-2's B chain, designed in 2016 to keep relaxin's anti-scarring effect in animal models. It has no human trials; this library's B7-33 entry records its evidence.