Cosyntropin

drug
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Also known as Corticotropin tetracosapeptideCortrosynCosyntropin acetateCosyntropin hexaacetateSynacthenSynacthen depotTetracosactidaTetracosactideTetracosactide acetateTetracosactide hexaacetateTetracosactide hexacetateTetracosactrinVicotrope

Summary

Cosyntropin (CHEMBL2103784) is an approved protein diagnostic agent (ATC H01AA02) targeting MC2R; indicated across 4 conditions including membranous glomerulonephritis and adrenal gland disorder.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Protein
  • ATC class: H01AA02
  • Targets: 1 (MC2R)
  • Indications: 4 conditions
  • Clinical trials: 19
  • Chemistry: 2933.4 Da · C136H210N40O31S

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2103784
NameCosyntropin
TypeProtein
Max phase4
FDA approvedno
PubChem CID16133802
ChEBICHEBI:3901
ATCH01AA02
Molecular formulaC136H210N40O31S
Molecular weight2933.4
InChIKeyZOEFCCMDUURGSE-SQKVDDBVSA-N

SMILES: CC(C)[C@@H](C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC2=CC=C(C=C2)O)C(=O)N3CCC[C@H]3C(=O)O)NC(=O)[C@@H]4CCCN4C(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](CC5=CNC6=CC=CC=C65)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC7=CC=CC=C7)NC(=O)[C@H](CC8=CNC=N8)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CO)NC(=O)[C@H](CC9=CC=C(C=C9)O)NC(=O)[C@H](CO)N

IUPAC name: (2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[2-[[(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-hydroxypropanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-hydroxypropanoyl]amino]-4-methylsulfanylbutanoyl]amino]-4-carboxybutanoyl]amino]-3-(1H-imidazol-4-yl)propanoyl]amino]-3-phenylpropanoyl]amino]-5-carbamimidamidopentanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]acetyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]acetyl]amino]hexanoyl]amino]hexanoyl]amino]-5-carbamimidamidopentanoyl]amino]-5-carbamimidamidopentanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]hexanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]pyrrolidine-2-carboxylic acid

ChEBI definition: A synthetic peptide that is identical to the 24-amino acid segment at the N-terminal of adrenocorticotropic hormone (corticotropin). A segment similar in all species, it contains the biological activity that stimulates production of corticosteroids in the adrenal cortex. It is used diagnostically to investigate adrenocortical insufficiency.

Pharmacological roles (ChEBI): diagnostic agent.

Also known as: Corticotropin tetracosapeptide, Cortrosyn, Cosyntropin, Cosyntropin acetate, Cosyntropin hexaacetate, Synacthen, Synacthen depot, Tetracosactida, Tetracosactide, Tetracosactide acetate, Tetracosactide hexaacetate, Tetracosactide hexacetate

Patent coverage: 2,066 distinct patent families (8,166 SureChEMBL compound mentions), from 4 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
MC2RMC2 receptorAgonist0%Q01718

Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Melanocortin receptor 4.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
MC4R9.19EC500.65nMCHEMBL_ACT_14729151

Target pathways

Aggregated over 1 target gene(s): MC2R.

Top Reactome pathways

10 total, by targets touching each:

PathwayTargetsGenes
Signal Transduction1MC2R
Disease1MC2R
Signaling by GPCR1MC2R
Class A/1 (Rhodopsin-like receptors)1MC2R
Peptide ligand-binding receptors1MC2R
GPCR downstream signalling1MC2R
G alpha (s) signalling events1MC2R
GPCR ligand binding1MC2R
Defective ACTH causes obesity and POMCD1MC2R
Diseases of metabolism1MC2R

Dominant GO biological processes

GO termTargets
G protein-coupled receptor signaling pathway1
G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger1
adenylate cyclase-activating G protein-coupled receptor signaling pathway1
signal transduction1
neuropeptide signaling pathway1

Indications & clinical

Indications

4 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
membranous glomerulonephritis2MONDO:0005376EFO:0004254
adrenal gland disorder1MONDO:0005495EFO:0005539
hypertensive disorder0MONDO:0005044EFO:0000537

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 19.

Phase distribution

PhaseTrials
Not specified8
PHASE44
PHASE23
PHASE12
PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00851942PHASE4COMPLETEDDetermination of Method-specific Normal Cortisol and Adrenal Hormone Responses to the Short Synacthen Test
NCT01371526PHASE4COMPLETEDRevival of Stem Cells in Addison’s Study
NCT02394457PHASE4COMPLETEDCosyntropin Versus Epidural Blood Patch (EBP) for Treatment of Treatment of Post Dural Puncture Headache
NCT03752190PHASE4WITHDRAWNComparison of Intramuscular and Intravenous ACTH Stimulation Test in Normal Volunteers
NCT03368066PHASE3COMPLETEDIs Adrenal Insufficiency Under-diagnosed in Hospitalized Cirrhosis Patients?
NCT03514589PHASE2RECRUITINGNeSST2: The Development of a Noninvasive Short Synacthen Test
NCT00694863PHASE2COMPLETEDTreatment With Synthetic ACTH in High Risk Patients With Membranous Nephropathy
NCT02813655PHASE2TERMINATEDEvaluation of the Effectiveness and Tolerance of Tetracosactide Synacthen® in the Treatment of Post Dural Puncture Headaches (ESYBRECHE)
NCT01673087PHASE1COMPLETEDStress Biomarkers:Attaching Biological Meaning to Field Friendly Salivary Measures
NCT01839812PHASE1COMPLETEDAdrenal Responsiveness During the Perioperative Period in Children Undergoing Congenital Cardiac Surgery
NCT01422733EARLY_PHASE1WITHDRAWNEffect of Longer-term Adrenal Suppression Using Low Dose Hydrocortisone on Androgen Overproduction
NCT00006270Not specifiedUNKNOWNStudy of the Approximate Entropy of Adrenocorticotropic Hormone and Cortisol Secretion in Patients With Head Injury
NCT00552487Not specifiedCOMPLETEDIsolated ACTH Deficiency in Patients With Hashimoto Thyroiditis
NCT01411046Not specifiedUNKNOWNDifference in GC-induced Adrenal Insufficiency in RA Related to Polymorphisms in the Glucocorticoid Receptor Gene
NCT01421797Not specifiedUNKNOWNEvaluation of Adrenal Androgens in Normal and Obese Girls After Suppression and Stimulation
NCT01764711Not specifiedCOMPLETEDAdrenocorticotropic Hormone Stimulation in Postural Orthostatic Tachycardia Syndrome (POTS)
NCT02339506Not specifiedCOMPLETEDStress and the Nervous System
NCT03136562Not specifiedCOMPLETEDPrevalence of Adrenal Insufficiency in Kidney Transplanted Patients in Glucocorticoid Treatment
NCT04642391Not specifiedCOMPLETEDDefining the Mechanisms Underlying Adrenal Insufficiency in Cirrhosis

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

1 molecules share ≥1 primary target. Top 1 by shared-target count:

MoleculeSourceStatusShared targets
ATUMELNANTChEMBLPhase 2MC2R