Overview
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In plain language
Insulin aspart is another fast-acting insulin analogue, made by Novo Nordisk and sold as NovoLog (NovoRapid). Like lispro it is injected right before a meal.
Scientists changed one amino acid in the middle of the B chain, replacing an asparagine with an aspartic acid. This small change also stops insulin molecules from pairing up, so it absorbs quickly after injection.
For students
Insulin aspart is human insulin with AsnB3 replaced by Asp (about 5,832 Da), a single negative-charge substitution that blocks dimer formation and speeds subcutaneous absorption (onset ~10-20 minutes, peak 1-3 hours, duration 3-5 hours).
Novo Nordisk later formulated a faster version, Fiasp, adding niacinamide (vitamin B3) and L-arginine to speed the initial absorption further, allowing dosing at the start of a meal. Aspart is a workhorse prandial insulin in pumps and multiple-injection regimens worldwide.
For researchers and instructors
Biochemistry. The B3 substitution sits at the dimer interface; introducing a negative charge at a hydrophobic contact point weakens self-association while leaving receptor-binding residues untouched.
Pharmacology. Absorption profile is similar to lispro; Fiasp's excipients roughly double early absorption rates in the first 30-60 minutes.
Human evidence. Registration trials demonstrated equivalent glycemic control with less postprandial hyperglycemia versus regular insulin; pump trials (including continuous glucose monitoring studies) support its use in closed-loop systems.
Teaching point. Shows that single-point mutations at aggregation interfaces, not the receptor-binding face, are enough to redesign insulin kinetics.
Molecular identity
- Amino acids
- 51 (A + B chains)
- Molecular weight
- ~5,832 Da
- Formula
- C₂₅₆H₃₈₇N₆₅O₇₉S₆
- Sequence
- Human insulin with B3 Asn replaced by Asp
Origin and history
Aspart, from Novo Nordisk, was approved in 2000. A single change, replacing asparagine with aspartic acid at position B3, stops the insulin molecules from pairing up. The result is a mealtime insulin that is absorbed faster and acts more briefly than regular human insulin.
A faster formulation, Fiasp, added niacinamide to speed absorption further.
Key people
- Novo Nordisk research teamDeveloped insulin aspart
Timeline
- 2000
NovoLog approved by the FDA
- 2017
Faster Fiasp formulation approved
See every peptide on one history timeline.
Human evidence
Comparison trials showed aspart lowers after-meal glucose better than regular insulin, with a similar safety profile.
Registration and enrollment are not proof of benefit; check study results directly.
Explore original publications and distinguish preclinical findings from controlled human evidence.
Safety and regulatory status
See every compound on the regulatory tracker.
FDA-approved. Errors in dosing cause low blood sugar; use only as prescribed.
This profile is educational and does not provide treatment, dosing or sourcing guidance.
Sources
- PubMed literature search: Insulin aspart
- PubChem compound search: Insulin aspart
- DailyMed (FDA label search): Insulin aspart
- UniProt search: Insulin aspart
- ClinicalTrials.gov search: Insulin aspart
Hernandez Gener, E. (November 8, 2026). Insulin aspart: molecular data, research history and evidence. VALREXA Biosciences. https://valrexa.com/peptides/insulin-aspart.html
APA style · Last reviewed November 8, 2026 · Our editorial standardsLast reviewed November 8, 2026. Trial and regulatory status can change; confirm in the linked registries. This profile is educational and is not medical advice, a treatment recommendation, or dosing or sourcing guidance. Report an error · Corrections policy
