Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=BWFPDJZCROQJEH-UHFFFAOYSA-N

Formula

C80H98N40O39P8S7

Mass

2716.12

Export to:

JSON SDF CSV

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

Previous Back Next