Structure Information
Structure

Compound Identification

SMILES

CCCN(C)C1=NC=NC2=C1N=CN2C1OC(CO)C(N)C1O

InChIKey

InChIKey=FIXXDVJTDKGXMQ-UHFFFAOYSA-N

Formula

C14H22N6O3

Mass

322.369

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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 - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Tetrahydrofuran - Azole - Imidazole - 1,3-aminoalcohol - Heteroaromatic compound - Secondary alcohol - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Primary aliphatic amine - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Amine - Primary alcohol - Primary amine - Organic nitrogen 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

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