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

CAS: 206055-69-8 Cat. No.: O648158 Molecular Weight: 255.23 PubChem CID: 22016714

Storage

Protected from light,Store at -80°C

Shipped In

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Overview

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

Biochemical and Physiological Mechanisms

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

Storage

Protected from light, Store at -80°C

Shipped In

Dry ice packs + Cold packs

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

Names and Identifiers

• Canonical Smiles: 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)
• Isomeric SMILES: C1C2(C(C(O1)C(O2)N3C=CC(=NC3=O)N)O)CO
• PubChem CID: 22016714
• Molecular Weight: 255.23

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: 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
• Description: 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