Structure Information
Structure

Compound Identification

SMILES

CC(NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1C[C@H](O)[C@@H](CO)O1)C(=C(/C1=CC=CC=C1)C1=CC=C(OCC[N+](C)(C)[O-])C=C1)\C1=CC=CC=C1

InChIKey

InChIKey=RITLFWMFYBGSGD-YHIAWQNYSA-N

Formula

C36H40N6O6

Mass

652.752

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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 - Stilbene - Diphenylmethane - 6-oxopurine - Hypoxanthine - Amphetamine or derivatives - Imidazopyrimidine - Phenylpropane - Purine - Phenoxy compound - Phenol ether - Alkyl aryl ether - Pyrimidone - Aminopyrimidine - Benzenoid - N-substituted imidazole - Pyrimidine - Monocyclic benzene moiety - Vinylogous amide - Azole - Heteroaromatic compound - Trialkyl amine oxide - Imidazole - Oxolane - Secondary alcohol - N-oxide - Ether - Oxacycle - Trisubstituted n-oxide - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Organic zwitterion - Organic salt - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Alcohol - 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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