PEPTIQORE QUALITY RECORD
PQ-PEP-000003
Liraglutide Quality Intelligence
Liraglutide is a GLP-1 receptor agonist analogue with a C16 fatty acid (palmitic acid) attached via a glutamic acid spacer to lysine at position 26. The fatty acid modification enables non-covalent albumin binding, extending the plasma half-life to approximately 13 hours and enabling once-daily dosing. Liraglutide shares 97% sequence homology with native GLP-1(7-37).
QUALITY RECORD
PQ-PEP-000003RECORD TYPE
Therapeutic Peptide
PEPTIQORE ID
PQ-PEP-000003
CAS NUMBER
204656-20-2
MOLECULAR WEIGHT
3751.2 Da
AMINO ACIDS
31
RECORD VERSION
1.1
RECORD COMPLETENESS
IDENTITY
Liraglutide Identity
Liraglutide is a GLP-1 receptor agonist analogue with a C16 fatty acid (palmitic acid) attached via a glutamic acid spacer to lysine at position 26 (Lys²⁶). The fatty acid modification enables non-covalent albumin binding, extending the plasma half-life to approximately 13 hours and enabling once-daily dosing. Liraglutide shares 97% sequence homology with native GLP-1(7-37), with a Lys³⁴→Arg³⁴ substitution and the Lys²⁶ fatty acid modification distinguishing it from the native peptide.
MOLECULAR FORMULA
C₁₇₂H₂₆₅N₄₃O₅₁
CALCULATED MW
3751.2 Da
CAS NUMBER
204656-20-2
AMINO ACID COUNT
31
QUALITY RISK MAP
QUALITY MAP
Liraglutide Quality Map
Relevant quality pathways and impurity categories. Data completeness varies by category.
Process-Related Impurities
Synthesis, modification, coupling, cleavage or purification
- Process-related impurity data under characterization
Custom analysis available.
Sequence-Related Impurities
Deletion, insertion, truncation and epimeric variants
- Sequence-related impurity data under characterization
Custom analysis available.
Degradation-Related Impurities
Oxidation, deamidation, hydrolysis and other degradation pathways
- Degradation data under characterization
Custom analysis available.
Based on published literature and regulatory data. Not all pathways necessarily occur in every batch.
IMPURITY LANDSCAPE
Liraglutide Impurities
Liraglutide Des-Fatty Acid Impurity
Liraglutide peptide backbone without the C16 fatty acid side chain. Loss of the palmitic acid modification via hydrolysis of the glutamic acid spacer linkage is a primary degradation and process-related impurity. This impurity has reduced albumin-binding affinity and altered pharmacokinetic profile.
Liraglutide Met Oxidation Impurity
Oxidation product at methionine residue(s) in the liraglutide sequence. Met oxidation is a well-characterised degradation pathway for GLP-1 analogues under oxidative stress conditions. The oxidised form may be detected by LC-MS as a +16 Da mass shift.
Liraglutide Deamidation Impurity
Deamidation product at asparagine or glutamine residue(s) in the liraglutide sequence. Deamidation introduces a +1 Da mass shift and may affect chromatographic retention. Relevant under acidic or elevated temperature stress conditions.
Liraglutide [Arg³⁴] Sequence Variant
Sequence variant with arginine at position 34. Liraglutide contains a Lys³⁴→Arg³⁴ substitution relative to native GLP-1(7-37); this impurity arises from incomplete or incorrect amino acid incorporation during synthesis. Reported in the scientific literature as a relevant process-related impurity.
ANALYTICAL DATA
Quality Data Overview
QUALITY GRAPH
Liraglutide Knowledge Graph
Connected quality knowledge — not a product catalog.
COMMERCIAL SUPPORT
Liraglutide Quality Support
Request Reference Material
Liraglutide parent or impurity reference material for analytical use.
Request Reference MaterialRequest Custom Synthesis
Custom synthesis of liraglutide-related impurities not in the standard catalog.
Request Custom SynthesisInvestigate Unknown Peak
Unexpected chromatographic peak in your liraglutide sample requiring investigation.
Investigate Unknown PeakSOURCES & EVIDENCE
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