Structure Information
Structure

Compound Identification

SMILES

CCCCN(CCCC)C=NC1=C2N=CN([C@@H]3O[C@H](CO)[C@@H](NC(=O)[C@H](CC4=CC=C(OC)C=C4)NC(=O)OCC4C5=CC=CC=C5C5=CC=CC=C45)[C@H]3O)C2=NC=N1

InChIKey

InChIKey=GMIRLNQAXCTRBR-OYGIVYLDSA-N

Formula

C44H52N8O7

Mass

804.949

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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 - Phenylalanine or derivatives - Fluorene - Alpha-amino acid amide - N-glycosyl compound - Glycosyl compound - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Pentose monosaccharide - Amphetamine or derivatives - Purine - Imidazopyrimidine - Phenol ether - Phenoxy compound - Anisole - Methoxybenzene - Alkyl aryl ether - Fatty acyl - Monosaccharide - Pyrimidine - Benzenoid - N-substituted imidazole - Fatty amide - Monocyclic benzene moiety - Imidazole - Oxolane - Carbamic acid ester - Azole - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Amidine - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid amidine - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Formamidine - Organic oxygen compound - Carbonyl group - Organic oxide - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Primary alcohol - 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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