Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](CC(=O)NC[C@H]3O[C@H](C[C@@H]3O)N3C=NC4=C3NC(N)=NC4=O)[C@@H](CO)O2)C(=O)NC1=O

InChIKey

InChIKey=DMVZEWPCYHVELH-SWTKMSQOSA-N

Formula

C22H28N8O8

Mass

532.514

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

2',5'-dideoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

2',5'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2',5'-dideoxyribonucleoside - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Tetrahydrofuran - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Secondary carboxylic acid amide - Urea - Amino acid or derivatives - Secondary alcohol - Carboxamide group - Lactam - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Alcohol - Organooxygen compound - Primary alcohol - Primary amine - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2',5'-dideoxyribonucleosides. These are nucleosides characterized by a purine or pyrimidine base, which is N-linked to a 2',5'-dideoxyribose moiety.

External Descriptors

Not available

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