Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2C2CC(OP(S)(=O)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3OP(O)(=S)OCC3OC(CC3O)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=CN=C4N)N3C=NC4=C3N=C(N)NC4=O)C(COP(O)(=S)OC3CC(OC3COP(O)(=S)OC3CC(OC3COP(O)(=S)OC3CC(OC3COP(O)(=S)OC3CC(OC3COP(O)(O)=O)N3C=NC4=C3N=CN=C4N)N3C=CC(N)=NC3=O)N3C=NC4=C3N=C(N)NC4=O)N3C=NC4=C3N=C(N)NC4=O)O2)C(=O)N1

InChIKey

InChIKey=LAGKVTPFJLXHBT-UHFFFAOYSA-N

Formula

C79H98N38O39P8S7

Mass

2676.09

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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 - 6-aminopurine - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Thiophosphate diester - Monoalkyl phosphate - Organic thiophosphoric acid or derivatives - Imidolactam - Alkyl phosphate - Thiophosphoric acid ester - Phosphoric acid ester - Organic phosphoric acid derivative - Pyrimidine - N-substituted imidazole - Hydropyrimidine - Azole - Heteroaromatic compound - Imidazole - Vinylogous amide - Oxolane - Lactam - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - 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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