Structure Information
Structure

Compound Identification

SMILES

CC1=CN(C2CC(OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(S)(=O)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3O)N3C=NC4=C3N=C(N)NC4=O)N3C=CC(N)=NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=C(N)NC4=O)N3C=C(C)C(=O)NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=C(C)C(=O)NC3=O)C(COP(O)(O)=S)O2)C(=O)NC1=O

InChIKey

InChIKey=HNEJGTFGNKXUJF-UHFFFAOYSA-N

Formula

C89H113N34O49P9S9

Mass

3010.38

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Thiophosphate diester - Pyrimidone - Imidolactam - Organic thiophosphoric acid or derivatives - Thiophosphate monoester - Hydropyrimidine - Pyrimidine - N-substituted imidazole - Thiophosphoric acid ester - Heteroaromatic compound - Vinylogous amide - Azole - Imidazole - Oxolane - Urea - Secondary alcohol - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxide - Alcohol - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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