Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2NCCCNC(=O)COC1=CC=C(\C=C\C2=CC=C3C=C4C=CC(C5=CC=CS5)=[N+]4[B-](F)(F)N23)C=C1

InChIKey

InChIKey=YJBAYXSDBZXYFO-HDNARQLNSA-N

Formula

C38H38BF2N9O6S

Mass

797.65

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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 - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Phenol ether - Phenoxy compound - Styrene - Alkyl aryl ether - Aminopyrimidine - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - N-substituted imidazole - Pyrimidine - Imidolactam - Oxolane - Heteroaromatic compound - Azole - Pyrrole - Thiophene - Imidazole - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - 1,2-diol - Oxacycle - Azacycle - Organic metalloid salt - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Alcohol - Carbonyl group - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic salt - Organic nitrogen compound - Organic zwitterion - Organonitrogen compound - Organooxygen 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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