Structure Information
Structure

Compound Identification

SMILES

CCCCCCSC[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=MQXLXVLOMJHMTA-YXDKPKCJSA-N

Formula

C21H35N7O4S

Mass

481.62

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