Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@H](OC(=O)C2=CC=CC=C2)[C@@H]1OC(=O)C1=CC=CC=C1)N1C=NC2=C1N=C(N=C2NCC(C1=CC=CC=C1)C1=CC=CC=C1)C(=O)NCCN1CCCCC1

InChIKey

InChIKey=BQPAJAJHULSIMD-CTBBXUKSSA-N

Formula

C48H50N8O7

Mass

850.977

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Diphenylmethane - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Benzoate ester - Imidazopyrimidine - Purine - Pyrimidine-2-carboxylic acid or derivatives - Benzoic acid or derivatives - 2-heteroaryl carboxamide - Benzoyl - Aminopyrimidine - Monocyclic benzene moiety - Pyrimidine - N-substituted imidazole - Benzenoid - Imidolactam - Piperidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Carboxamide group - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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