Structure Information
Structure

Compound Identification

SMILES

CCOP(=O)(CC(=O)C[C@@H]1[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@H]([C@@H]1O[Si](C)(C)C(C)(C)C)N1C=NC2=C1N=CN=C2N)OCC

InChIKey

InChIKey=UUQMONJCUBRTLW-SPEYYTFGSA-N

Formula

C29H54N5O7PSi2

Mass

671.923

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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 - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl alkylphosphonate - Phosphonic acid diester - N-substituted imidazole - Phosphonic acid ester - Pyrimidine - Imidolactam - Heteroaromatic compound - Azole - Imidazole - Trialkylheterosilane - Oxolane - Organophosphonic acid derivative - Silyl ether - Ketone - Organoheterocyclic compound - Oxacycle - Azacycle - Organic metalloid salt - Organoheterosilane - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic metalloid moeity - Organic nitrogen compound - Organophosphorus compound - Amine - Primary amine - Carbonyl group - Organic oxide - Organic oxygen compound - Organosilicon 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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