Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1CC[C@@H](O1)N1C=NC2=C1NC=NC2=O.CCCC1=CC(=O)OC2=C1C1=C(C=CC(C)(C)O1)C1=C2[C@@H](O)[C@H](C)[C@@H](C)O1

InChIKey

InChIKey=MCWCOJVMUJAJQR-ZALWWLMDSA-N

Formula

C32H38N4O8

Mass

606.676

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2',3'-dideoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2',3'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Not available

Substituents

Purine 2',3'-dideoxyribonucleoside - Pyranocoumarin - Angular pyranocoumarin - Pyranochromene - 2,2-dimethyl-1-benzopyran - Coumarin - Purinone - Benzopyran - Chromane - 6-oxopurine - 1-benzopyran - Hypoxanthine - Imidazopyrimidine - Purine - Pyrimidone - Pyranone - Alkyl aryl ether - N-substituted imidazole - Benzenoid - Pyran - Pyrimidine - Vinylogous amide - Tetrahydrofuran - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Lactone - Organoheterocyclic compound - Azacycle - Ether - Oxacycle - Alcohol - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organic oxygen compound - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2',3'-dideoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.

External Descriptors

Not available

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