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ChemicalBook--->CAS DataBase List--->876708-01-9

876708-01-9

876708-01-9 Structure

876708-01-9 Structure
IdentificationBack Directory
[Name]

2,4(1H,3H)-PyriMidinedione, 1-(4-C-azido-β-D-arabinofuranosyl)- (9CI)
[CAS]

876708-01-9
[Synonyms]

CS-M1996
Nucleoside-Analog-2
Nucleoside Analog 2,NucleosideAnalog2
2,4(1H,3H)-PyriMidinedione, 1-(4-C-azido-β-D-arabinofuranosyl)- (9CI)
[Molecular Formula]

C9H11N5O6
[MOL File]

876708-01-9.mol
[Molecular Weight]

285.22
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[form ]

Solid
[color ]

Light brown to gray
[Water Solubility ]

Water : 20 mg/mL (70.12 mM)
Hazard InformationBack Directory
[Description]

Nucleoside-Analog-2 is a 4'-Azidocytidine analogue against Hepatitis C virus (HCV) replication.

Nucleoside-Analog-2 is a 4'-Azidocytidine analogue against Hepatitis C virus (HCV) replication. Reference to compound 12[1].

[Uses]

Nucleoside-Analog-2 is a 4'-Azidocytidine analogue against Hepatitis C virus (HCV) replication. Nucleoside-Analog-2 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
[storage]

Store at -20°C
[References]

[1]. Smith DB, et al. The design, synthesis, and antiviral activity of 4'-azidocytidine analogues against hepatitis C virus replication: the discovery of 4'-azidoarabinocytidine. J Med Chem. 2009 Jan 8;52(1):219-23.

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