Structure Information
Structure

Compound Identification

SMILES

CN(CCCN(C)C(=O)CC1=CC=C(C=C1)C(C)(C)C)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=PTLVHTGBHNPUHN-VJUOEERUSA-N

Formula

C27H39N7O4

Mass

525.654

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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 - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Phenylacetamide - Imidazopyrimidine - Phenylpropane - Purine - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Oxolane - Tertiary carboxylic acid amide - Azole - Imidazole - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - 1,2-diol - Carboxamide group - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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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