Structure Information
Structure

Compound Identification

SMILES

C[C@@H](N)C(=O)N[C@@H]1[C@@H](CO)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN=C2N(C)C

InChIKey

InChIKey=HJGKTJRKKXMHKK-PHFBBPMTSA-N

Formula

C15H23N7O4

Mass

365.394

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Alpha-amino acid amide - Alanine or derivatives - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Imidolactam - Pyrimidine - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Organooxygen compound - Alcohol - Organic oxygen compound - Primary amine - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Amine - Primary aliphatic amine - Organic oxide - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

Previous Back Next