PEPTIDE CORPUS

Cardiovascular & General

Elabela

Elabela was found in 2013 as a second, unsuspected signal at the receptor apelin already uses, and it turned out to be indispensable: an embryo that cannot make it does not build a normal heart or blood vessels. In adult mice with pressure-overloaded, failing hearts, continuous infusion of it suppressed muscle thickening, scarring and loss of pumping strength, and the effect disappeared entirely in mice bred without the receptor — about as clean as an animal causal argument gets. It has never been given to a human being. The corpus record for it is marked preclinical only.

Last updated

Studied forCardiovascular research · Renal function research · Developmental biology context
Strongest sourceTherapeutic potential of ELABELA in alleviating hereditary hypertrophic cardiomyopathy. (animal study)

Mechanism

Binds and activates the apelin receptor (APJ), a G-protein-coupled receptor governing vascular tone and cardiac contractility.

Reported effects

What sources associate with this compound. Reported categories, not outcomes we have graded — each would need its own citation and rung.

  • Cardiovascular research
  • Renal function research
  • Developmental biology context

Dosing on file unverified

No established human dose; animal: 10 nmol/kg/hr, 39 µg/kg/hr

Carried from a source that labels it unverified, and reproduced with that label attached. A record of what is reported, not a recommendation. No citation on this page establishes it.

Half-life, storage & sport

Elimination half-life
13 min (mice) — study. Frontiers in pharmacology 2025; mice, the native ELA-21 peptide (the comparator to the Fc-ELA-21 fusion in the same sentence).

The half-life on file is 13 min, measured in mice. No dosing schedule could be read from this record, so the curve below is one dose drawn from the moment it is given. Nothing here says how often it is repeated.

One dose. 1.1 h of decay, normalised to its own peak.
1 compounds on one time axis, each normalised to its own peak0%25%50%75%100%0 min16 min33 min49 min1.1 hpeaktime from the first doseElabela

The measurement is not human. It was made in mice, and small mammals clear peptides faster than people do — so this is the fastest plausible shape rather than the expected one.

The rise is not modelled and the axis is not a blood level. No absorption rate constant and no volume of distribution are on file, so each dose appears at full height the instant it is given, and the axis is percent of this compound's own peak.

Literature on file 5

Notes unverified prose

No human clinical trials identified; animal models only; not for human use; No human clinical trials; preclinical

Not on file 9

8 of the 8 fields we track hold nothing on this record, and each says why. 1 further absence is named below. A blank field is a bug; a named absence is a finding.

Each field links to every other record missing the same thing. The full ledger holds 765 gaps across 163 records.