Cosyntropin

FDA-approved ACTH(1-24) diagnosticEstablished

Cosyntropin is a research peptide in the Melanocortin receptor agonist class. The N-terminal 24 residues of ACTH carry its full biological activity at the melanocortin-2 receptor of the adrenal cortex, while the omitted C-terminal residues account for most of the immunogenicity of the full hormone.

Calculate Dose

For research use only.

Key Facts

CAS
16960-16-0
Molecular Weight (MW)
2933.4 g/mol
Half-life
FDA status
Approved
Administration Route
intravenous, intramuscular
Frequency
Last updated
Aug 30, 2026
Reviewed
Aug 30, 2026

Research summary

Synthetic peptide comprising the first 24 amino acids of corticotropin, approved as a diagnostic agent for screening adrenocortical insufficiency. It is a diagnostic tool rather than a therapy.

Peptide Library's Cosyntropin profile summarises 5 cited studies listed in the Science section, the compound's regulatory status, and research-protocol parameters reported for it. It is a research reference, not medical advice.

Protocol

Dosage Range
Frequency
Cycle
Administration Route
intravenous, intramuscular
Reconstitution Guide

Not yet checked against primary sources

These figures are compiled from earlier reference material. They have not been verified against FDA labelling, registered trials or published literature, no citation is attached to them, and none of them is a recommended dose. Cosyntropin is queued for dosage evidence review.

Compare reported doses across the whole library

Sequence & molecular data

Sequence and molecular data for Cosyntropin
Molecular formulaC136H210N40O31S
Molecular weight2933.4 g/mol
CAS number16960-16-0
PubChem CID16129617

Identifiers link to the public PubChem, FDA Substance Registration (UNII), ChEMBL and DrugBank records for the same entity.

Science

Mechanism of Action

The N-terminal 24 residues of ACTH carry its full biological activity at the melanocortin-2 receptor of the adrenal cortex, while the omitted C-terminal residues account for most of the immunogenicity of the full hormone. Receptor activation raises cyclic AMP and stimulates steroidogenesis, so the cortisol rise after a measured dose reports the adrenal cortex’s capacity to respond.

Regulatory & research status

Cosyntropin is an FDA-approved product for specific labelled indications. Approval does not extend to the research contexts described on this page, and approved products are prescription medicines.

Regulatory and research status for Cosyntropin
FDA statusApproved
Research statusApproved product (see FDA status)
AvailabilityPrescription-Only
WADA (sport)Unknown / Not Listed
Library classificationFDA-Approved

Benefits

Potential Side Effects

No side effects listed yet for this entry.

Storage & stability

Lyophilized (freeze-dried) peptide powder is far more stable than the reconstituted solution. Keep sealed vials cold, dry and away from light; long-term storage is typically frozen, with short-term refrigeration for vials in use.

Once reconstituted in bacteriostatic water, keep the solution refrigerated, avoid repeated freeze–thaw cycles and agitation, and label the vial with the reconstitution date and concentration. Discard any solution that turns cloudy or shows particulates.

Degradation rates differ by sequence: peptides containing methionine, cysteine, asparagine or glutamine are more prone to oxidation and deamidation, so shelf life after reconstitution is compound-specific rather than universal.

Read the full guide: how to store peptides before and after reconstitution →

Source: Manning MC, Chou DK, Murphy BM, Payne RW, Katayama DS. Stability of protein pharmaceuticals: an update. Pharm Res. 2010;27(4):544–575. (PMID 20143256). General guidance for research handling; not product-specific instructions.

Cosyntropin: frequently asked questions

What is Cosyntropin?

Synthetic peptide comprising the first 24 amino acids of corticotropin, approved as a diagnostic agent for screening adrenocortical insufficiency. It is a diagnostic tool rather than a therapy.

How does Cosyntropin work?

The N-terminal 24 residues of ACTH carry its full biological activity at the melanocortin-2 receptor of the adrenal cortex, while the omitted C-terminal residues account for most of the immunogenicity of the full hormone. Receptor activation raises cyclic AMP and stimulates steroidogenesis, so the cortisol rise after a measured dose reports the adrenal cortex’s capacity to respond.

Is Cosyntropin FDA approved?

Yes. Cosyntropin is approved by the FDA, and approved products are prescription medicines. Approval is always for specific indications studied in clinical trials, so an approved status does not mean the compound is approved for every use it is discussed for. Research-chemical material sold under the same name is not the approved product.

What peptides are similar to Cosyntropin?

Compounds most often compared with Cosyntropin include Bremelanotide, Melanotan II, Angiotensin II and Cetrorelix. They are grouped by shared mechanism or research area rather than by equivalence, and their regulatory status and evidence base differ.

References

Related research, comparisons & guides

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Compiled by Peptide Library Editorial · Reviewed Aug 30, 2026 · Updated Aug 30, 2026 · Version 1

This Cosyntropin profile is compiled from published literature (5 cited studies linked above), public regulatory records and chemical registries. It describes what research reports; it is not medical advice, and nothing here is a dosing recommendation for humans. Peptide Library does not sell peptides. Editorial policy · How profiles are compiled · Report an error

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