Semaglutide, CAS No.910463-68-2

CAS: 910463-68-2 Cat. No.: S774153 Molecular Weight: 4113.58 EC Number: 691-729-9

GRADE & PURITY Animal Free, Carrier Free, PharmPure™, Endotoxin tested, ≥99%

Accession #

P01275

Expression system

E. coli

Specifications

Product Name

Semaglutide, CAS No.910463-68-2

Grade

Animal Free, Carrier Free, Endotoxin tested, PharmPure™

Specifications & Purity

Animal Free, Carrier Free, PharmPure™, endotoxin tested, ≥99%

Sequence

His-Aib-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly

Accession #

P01275

Predicted molecular weight

4113.58 Da

CAS

910463-68-2

Molecule Type

Protein

Storage and Shipping

Storage

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

Shipped In

Ice chest + Ice pads

Stability And Storage

Store at -20℃ (5 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
    • Class Polypeptides

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

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

References

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2. Junxia Zhang, Changyun Liu, Yupeng Wang, Yusi Chen, Haibao Shang, Wen Zheng, Li Jin, Peng Xie, Yingjia Li, Yahan Liu, Yunxiao Zhang, Yang Wang, Wei Zhao, Han Xiao, Guisong Wang, Xin Zhang, Xiaolei Yang, Erdan Dong, Yan Zhang.  (2026)  Bacteroides acidifaciens exacerbates cardiac ischemia/reperfusion injury via the microbial-host isozyme DPP4.  Cell Host & Microbe,      [PMID:41923637] [10.1016/j.chom.2026.03.012]