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Cagrilintide
Also indexed as AM833, NN9838, cagrilintide acetate
1 Identity
Incretin and amylin receptor agonists. component of the fixed combination marketed in development as CagriSema. CAS 1415456-99-3.
- Sequence
- {Eicosanedioic acid-gamma-Glu}-Lys-Cys-Asn-Thr-Ala-Thr-Cys-Ala-Thr-Gln-Arg-Leu-Ala-Glu-Phe-Leu-Arg-His-Ser-Ser-Asn-Asn-Phe-Gly-Pro-Ile-Leu-Pro-Pro-Thr-Asn-Val-Gly-Ser-Asn-Thr-Pro-NH2, with a disulfide bridge between the two cysteines (Cys3-Cys8 in the supplier's numbering, which counts the gamma-Glu as position 1; these are the 2nd and 7th amino-acid residues of the chain). THIRTY-seven residues, not 32; the 32-residue backbone figure that circulates for this molecule is wrong.
- Molecular formula
- C194H312N54O59S2
- Average mass
- 4409.069 Da (C194H312N54O59S2) from the formula. Listings commonly print 4409.07.
- Monoisotopic mass
- 4406.2515 Da neutral. Practical charge states: [M+4H]4+ m/z 1102.5702, [M+5H]5+ m/z 882.2576, [M+6H]6+ m/z 735.3825.
- Salt / variant note
- Adding two AEEA (8-amino-3,6-dioxaoctanoic acid) units gives C206H334N56O65S2, 4699.39 avg / 4696.3993 mono - 290.3 Da heavier than the real article. That linker architecture belongs to semaglutide-class molecules, not to cagrilintide, whose linker is gamma-Glu alone. Genuine commercial and analytical variants: (1) free base versus acetate, sold as separate catalog items by more than one institutional supplier and deposited as separate PubChem records (CID 171397054 and CID 164618153); acetate stoichiometry is written as X by those suppliers, so net peptide is undeclared at the catalog level. (2) ring-open, fully reduced material, C194H314N54O59S2, 4411.085 avg / 4408.2672 mono, +2.016 Da - and note that this number sits within 0.009 Da of PubChem's erroneous exact mass, so a certificate printing 4408.26 is indistinguishable on its face from a reduced lot. (3) free-acid C-terminus (amidation failure), C194H311N53O60S2, 4410.053 avg / 4407.2355 mono, +0.984 Da. (4) des-acyl backbone with the eicosanedioyl-gamma-Glu unit absent entirely, C169H269N53O53S2, 3955.449 avg / 3952.9425 mono, -453.62 Da. (5) near-neighbor amylins: native human amylin near 3903, pramlintide near 3949 - both within the range a low-resolution deconvolution could confuse with the des-acyl species. (6) Scrambled-disulfide and dimeric species at the same or double nominal mass.
2 Class & testing panel
- Form
- Single article
- Testing panel
- P2 — panel definition
3 Primary sources & evidence
A substantial sponsor-run clinical program exists and is registered. Cagrilintide has been studied by Novo Nordisk A/S in phase 1 and phase 2 trials as a single agent and in fixed combination with semaglutide, with the combination program registered on ClinicalTrials.gov under the REDEFINE series and reported in general medical journals from 2021 onward; a phase 2 report of cagrilintide monotherapy appeared in The Lancet in 2021. This is a description of what has been registered and published, by study type and sponsor. No United States marketing authorization exists for cagrilintide as a single agent as of August 2026. No pharmacopoeial monograph exists.
4 Storage & specification
- Storage
- Lyophilized powder, -20 degrees C plus or minus 5 degrees C, desiccated, protected from light.
- Shelf life
- Provisional 24 months at -20 degrees C plus or minus 5 degrees C.
This record reports identity, specification and study design. It does not state what the article does in a human body. Supplied under the caution: “CAUTION: Contains a new drug for investigational use only in laboratory research animals or for tests in vitro. Not for use in humans.”
