Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](CN2N=CC=N2)O[C@H]([C@@H]1OC=O)N1C=NC2=C(NCC(C3=CC=CC=C3)C3=CC=CC=C3)N=C(NCCN3CCOCC3)N=C12

InChIKey

InChIKey=LFUBYOUFVFUPJB-DWCTZGTLSA-N

Formula

C33H38N10O5

Mass

654.732

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Diphenylmethane - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - Morpholine - N-substituted imidazole - Oxazinane - Monocyclic benzene moiety - Pyrimidine - Imidolactam - Benzenoid - Oxolane - Azole - 1,2,3-triazole - Heteroaromatic compound - Imidazole - Amino acid or derivatives - Carboxylic acid ester - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Oxacycle - Carboxylic acid derivative - Azacycle - Dialkyl ether - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Alcohol - Carbonyl group - Organic nitrogen compound - Amine - Organic oxygen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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