Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCCCCNC(=O)CC[N+](C)=C1C=CC2=NC3=C(OC2=C1)C=C(C=C3)N(CC)CCCS([O-])(=O)=O

InChIKey

InChIKey=SEHPCAUSPLKMGO-DEGFIOCKSA-N

Formula

C37H48N10O9S

Mass

808.91

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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 - Phenoxazine - Beta amino acid or derivatives - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Purine - Imidazopyrimidine - Dialkylarylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Imidolactam - Benzenoid - N-substituted imidazole - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Secondary ketimine - Azole - Oxolane - Alkanesulfonic acid - Heteroaromatic compound - Imidazole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Secondary amine - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Azacycle - Organic oxygen compound - Organic salt - Organic zwitterion - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organosulfur compound - Amine - Organic nitrogen compound - Organonitrogen compound - 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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