2'-O,4'-C-Methylenecytidine , CAS No.206055-69-8

CAS: 206055-69-8 Cat. No.: O648158 Peso molecular: 255.23 PubChem CID: 22016714

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

2'-O,4'-C-Methylenecytidine (LNA-C(Bz)) is a bicyclic nucleoside analogue with fixed N-type conformation. 2'-O,4'-C-Methylenecytidine can be used to synthesize oligonucleotides. 2'-O,4'-C-Methylenecytidine forms duplexes with complementary DNA and RNA strands.

Form:Solid

Specifications

Mecanismos bioquímicos y fisiológicos

2'-O, 4'-C-Methylenecytidine (LNA-C(Bz)) is a bicyclic nucleoside analogue with fixed N-type conformation. 2'-O, 4'-C-Methylenecytidine can be used to synthesize oligonucleotides . 2'-O, 4'-C-Methylenecytidine forms duplexes with complementary DNA and RNA st

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: C1C2(C(C(O1)C(O2)N3C=CC(=NC3=O)N)O)CO
• IUPAC Name: 4-amino-1-[7-hydroxy-1-(hydroxymethyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl]pyrimidin-2-one
• InChIKey: FCMRQQIZHFHCNG-UHFFFAOYSA-N
• INCHI: 1S/C10H13N3O5/c11-5-1-2-13(9(16)12-5)8-6-7(15)10(3-14,18-8)4-17-6/h1-2,6-8,14-15H,3-4H2,(H2,11,12,16)
• Isómeros SMILES: C1C2(C(C(O1)C(O2)N3C=CC(=NC3=O)N)O)CO
• PubChem CID: 22016714
• Peso molecular: 255.23

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 Glycosylamines

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: Glycosylamines
• Alternative Parents: Pyrimidones Aminopyrimidines and derivatives 1,4-dioxanes Hydropyrimidines Imidolactams Monosaccharides Heteroaromatic compounds Oxolanes Secondary alcohols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Primary amines Primary alcohols Hydrocarbon derivatives Organic oxides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: N-glycosyl compound - Aminopyrimidine - Pyrimidone - Para-dioxane - Hydropyrimidine - Monosaccharide - Imidolactam - Pyrimidine - Heteroaromatic compound - Oxolane - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
• 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