Liraglutide, CAS No.204656-20-2

CAS: 204656-20-2 Cat. No.: L774154 Formula: C₁₇₂H₂₆₅N₄₃O₅₁ Peso molecolare: 3751.2 Numero EC: 810-818-7

GRADE & PURITY ≥99%

Accession #

P01275

Expression system

E. coli

Endotoxin Concentration

<10 EU/mg

Specifications

Product Name

Liraglutide, CAS No.204656-20-2

Specifiche e purezza

≥99%

Concentrazione di endotossina

<10 EU/mg

Numero d'ordine

P01275

Peso molecolare previsto

3751.2 Da

CAS

204656-20-2

Tipo di molecola

Proteine

Proprietà del prodotto

• ALogP: -3.4

Stoccaggio e spedizione

Condizioni di conservazione di stoccaggio

Protected from light,Store at -20°C,Desiccated,Avoid repeated freezing and thawing

Spedito in

Ice chest + Ice pads

Stabilità e conservazione

Store at -20℃ (3 years). Store in the dark. Desiccated. Upon receipt, it is recommended to aliquot. Avoid freeze/thaw cycle.

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic Polymers
    • Classe Polypeptides

• Kingdom: Organic compounds
• Superclass: Organic Polymers
• Classe: Polypeptides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Polypeptides
• Alternative Parents: Hexacarboxylic acids and derivatives Peptides Tyrosine and derivatives Phenylalanine and derivatives Arginine and derivatives Histidine and derivatives Glutamine and derivatives Glutamic acid and derivatives Aspartic acid and derivatives Isoleucine and derivatives Leucine and derivatives N-acyl-L-alpha-amino acids Valine and derivatives Serine and derivatives Tryptamines and derivatives Alpha amino acid amides Alanine and derivatives 3-alkylindoles Amphetamines and derivatives Imidazolyl carboxylic acids and derivatives 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Substituted pyrroles N-acyl amines Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Amino acids Primary carboxylic acid amides Guanidines Azacyclic compounds Carboximidamides Carboxylic acids Organopnictogen compounds Primary alcohols Monoalkylamines Imines Carbonyl compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Polypeptide - Hexacarboxylic acid or derivatives - Alpha peptide - Tyrosine or derivatives - Arginine or derivatives - Phenylalanine or derivatives - Histidine or derivatives - Glutamic acid or derivatives - Glutamine or derivatives - Aspartic acid or derivatives - Isoleucine or derivatives - Leucine or derivatives - Valine or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Triptan - Serine or derivatives - Alpha-amino acid amide - Alanine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - 3-alkylindole - Indole - Indole or derivatives - Imidazolyl carboxylic acid derivative - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Substituted pyrrole - N-acyl-amine - Fatty acyl - Fatty amide - Azole - Heteroaromatic compound - Imidazole - Pyrrole - Primary carboxylic acid amide - Amino acid or derivatives - Secondary alcohol - Secondary carboxylic acid amide - Amino acid - Carboxamide group - Guanidine - Carboximidamide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Primary alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Imine - Carbonyl group - Primary aliphatic amine - Alcohol - Organic oxide - Organopnictogen compound - Amine - Organooxygen compound - Organonitrogen compound - Primary amine - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues.
• External Descriptors: lipopeptide - polypeptide

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Riferimenti

1. Jiahao Wang, Lei Peng, Haoran Sun, Jie Zeng, Rui Fu, Haonan Zhang, Rong Liang, Yan Lin, Jiazhou Ye, Liang Ma, Xiaoling Luo, Heng Jiang, Guobin Wu, Bo Qian, Rongyun Mai.  (2026)  Amygdalin Alleviates MAFLD via Inhibiting Cytoplasmic Calcium Ion Overload-Induced Liver Sinusoidal Endothelial Cell Defenestration.  PHYTOMEDICINE,      [PMID:41962269] [10.1016/j.phymed.2026.158135]

2. Gao Jie, Lv Xiaoyu, Zhao Pingping, Pan Bingjing, Liu Jingfang.  (2026)  Liraglutide affects mitochondrial function and histone acetylation through the NQO1/SIRT3 pathway in diabetic kidney disease.  MOLECULAR AND CELLULAR BIOCHEMISTRY,      [PMID:] [10.1007/s11010-026-05670-3]

3. Liu Yiran, Liu Xiao, Yin Xueyong, Li Yunluo, Yu Xiaohui, Nan Xinyu, Xue Jiping, Lu Hengtai, Li Bingyu, Zhou Fei, Liu Xiaoyu, Zhang Xiangyu, He Xiangjun, Yu Xi, Yan Shu, Li Yating, Wang Shuang, Gao Yuan, Liu Yifan, Kang Ying, Zhang Jingwen, Zhao Ye, Shi Haishui.  (2026)  Activation of GLP-1 receptors suppresses pathological defensive aggression via DMPAG in mice.  Translational Psychiatry,      [PMID:] [10.1038/s41398-026-04385-9]