Peptidoglycan，from Staphylococcus aureus - BioReagent, used for Peptidoglycan from Staphylococcus aureus has been used: for the stimulation of lymphocytes: peptidoglycan activates the toll-like receptor 2 (TLR2), present in mammalian cells. It works as an

CAS: 27814-48-8 Cat. No.: P1520672 EC Number: 229-698-7 PubChem CID: 93035

GRADE & PURITY BioReagent

Synonyms

Peptidoglycan from S. aureus | PGN

Storage

Store at -20°C,Argon charged,Desiccated

Shipped In

Ice chest + Ice pads

Specifications

Synonyms

Peptidoglycan from S. aureus | PGN

Specifications & Purity

BioReagent

Biochemical and Physiological Mechanisms

The cell wall of gram positive bacteria is largely made up of peptidoglycan. It is composed of polysaccharide chains interlinked by peptide bridges. This peptidoglycan gives a certain rigidity to the cell wall and gives the cell mechanical strength. It is

Application

Peptidoglycan from Staphylococcus aureus has been used: for the stimulation of lymphocytes: peptidoglycan activates the toll-like receptor 2 (TLR2), present in mammalian cells. It works as an antagonist of Poly (I:C) for g-type lysozyme stimulation by int

Storage

Store at -20°C,Argon charged,Desiccated

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

BioReagent

Names and Identifiers

Pubchem Sid

516568244

Canonical Smiles

C1C(O1)CO[N+](=O)[O-]

InChIKey

ADZAAKGRMMGJKM-UHFFFAOYSA-N

INCHI

1S/C3H5NO4/c5-4(6)8-2-3-1-7-3/h3H,1-2H2

Isomeric SMILES

C1C(O1)CO[N+](=O)[O-]

Alternate CAS

6659-62-7,27814-48-8

PubChem CID

93035

NSC Number

137875

MeSH Entry Terms

glycidyl nitrate

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organic oxoanionic compounds
      • Subclass Organic nitrates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organic oxoanionic compounds
• Subclass: Organic nitrates
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkyl nitrates
• Alternative Parents: Organic nitro compounds Organic nitric acids and derivatives Oxacyclic compounds Epoxides Dialkyl ethers Organic oxides Organic nitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Alkyl nitrate - Organic nitro compound - Organic nitric acid or derivatives - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Ether - Oxirane - Dialkyl ether - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as alkyl nitrates. These are organic compounds containing a nitrate that is O-linked to an alkyl group.
• 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

Chemical and Physical Properties

• Sensitivity: Moisture sensitive
• Molecular Weight: 119.080 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 119.022 Da
• Monoisotopic Mass: 119.022 Da
• Topological Polar Surface Area: 67.600 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 97.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1