Catalog classification, reference sizes, lab math links, and source-backed data. Educational use only — not medical advice.
Researched for: PepTools vendor-neutral scientific reference catalog
Also known as: Degludec, NN1250, NN-1250, DA-74494, Tresiba
Insulin degludec is a recombinant long-acting human insulin analog. Compared with human insulin, threonine at position B30 is omitted and a glutamic-acid-linked C16 fatty-acid side chain is attached to LysB29. After subcutaneous administration, the modified insulin forms a depot of multi-hexamers, from which insulin monomers are gradually released into the circulation. It is supplied as clear, colorless solutions at 100 units/mL and 200 units/mL.
Source review pending. This descriptive profile is shown from the available source material as a best-effort educational reference. It has not passed the full verification bar and is not a dosing instruction, medical claim, or treatment recommendation.
Reflects preclinical/research literature context only. Not a medical claim, dosing instruction, or treatment recommendation.
Insulin degludec is a peptide biologic rather than a small molecule. Its prolonged action is attributed primarily to delayed absorption from the subcutaneous multi-hexamer depot, with additional contribution from reversible albumin binding. FDA labeling describes subcutaneous administration only and states that the product should not be administered intravenously or by insulin infusion pump. Evidence-backed clinical pharmacology studies have evaluated doses including 0.4, 0.6, and 0.8 units/kg under euglycemic-clamp conditions; these are study regimens and are not individualized dosing recommendations.
Supplementary research context only. Not medical advice or a treatment recommendation.
CAS RN 844439-96-9; PubChem CID 118984462; molecular formula C274H411N65O81S6; molecular weight 6.104 kDa; DrugBank ID DB09564; ATC code A10AE06
The U-100 and U-200 formulations provide comparable exposure and glucose-lowering effect when administered at the same unit-per-kilogram dose. FDA labeling reports median onset of appearance of approximately 1 hour after the first subcutaneous dose and median maximum concentration at approximately 9 hours after repeated once-daily dosing in adults with type 1 diabetes. Steady-state concentrations are reached after approximately 3–4 days of administration.
Reflects published research. Educational reference — not a recommendation for use.
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Published articles on this site that mention Insulin degludec or one of its catalog aliases.
Research Use Only. All content is for educational and research reference only. Not medical advice, a treatment recommendation, or guidance on human use. Compounds are not FDA-approved drugs unless specifically noted.