Heparin sodium - ≥95%(HPLC), wt3,000-5,000 , CAS No.9041-08-1

CAS: 9041-08-1 Cat. No.: H758710 Numero EC: 618-546-9 PubChem CID: 118989588

GRADE & PURITY ≥95%(HPLC), wt3,000-5,000

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

The specific biological function of heparin is achieved through the interaction between specific functional regions within its sugar chain and target proteins. For example, heparin molecules can inhibit factor Xa through the interaction between the special five sugar structure GlcNAc/NS (6S) - GlcA GlcNS (3S, 6S) - IdoA (2S) - GlcNS (6S) within the sugar chain and antithrombin ATIII. In order to meet the needs of customers for studying the structure-activity relationship of various glycosaminoglycans, we used heparanase I/II to partially degrade heparin, and prepared heparin oligosaccharides and low molecules with different polymerization degrees through gel filtration and ion exchange HPLC. At the same time, we can also customize heparin oligosaccharides and low molecular weight compounds with special structural requirements for customers by utilizing various unique structural selective degradation enzymes and modification enzymes according to their needs.

Specifications

Specifiche e purezza

≥95%(HPLC), wt3,000-5,000

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%(HPLC)

Nomi e identificatori

Sorrisi canonici

C1N(CN(CN1CCO)CC[O-])CCO.[Na+]

IUPAC Name

sodium;2-[3,5-bis(2-hydroxyethyl)-1,3,5-triazinan-1-yl]ethanolate

InChIKey

YOMTXLQWRQUKAK-UHFFFAOYSA-N

INCHI

1S/C9H20N3O3.Na/c13-4-1-10-7-11(2-5-14)9-12(8-10)3-6-15;/h13-14H,1-9H2;/q-1;+1

Isomeri SMILES

C1N(CN(CN1CCO)CC[O-])CCO.[Na+]

WGK Germania

2

RTECS

MI0850000

PubChem CID

118989588

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Triazinanes
      • Subclass 1,3,5-triazinanes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Triazinanes
• Subclass: 1,3,5-triazinanes
• Intermediate Tree Nodes: Not available
• Direct Parent: 1,3,5-triazinanes
• Alternative Parents: Azacyclic compounds Alkanolamines Organopnictogen compounds Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Alkoxides Alcohols and polyols
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 1,3,5-triazinane - Azacycle - Organic alkali metal salt - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organic zwitterion - Alkoxide - Organooxygen compound - Organonitrogen compound - Alcohol - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as 1,3,5-triazinanes. These are triazinanes having three nitrogen ring atoms at the 1-, 3-, and 5- positions.
• 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