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Structure Information
Structure

Compound Identification

SMILES

COC1(CCN(CC1)C1=CC=CC=C1F)O[C@@H]1[C@H](O)[C@@H](CO[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)O[C@H]1N1C=NC2=C1NC(\N=C\N(C)C)=NC2=O

InChIKey

InChIKey=IQMWBSHGZFMYFY-ONZVRGSXSA-N

Formula

C41H50FN7O6Si

Mass

783.977

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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 - Phenylpiperidine - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Imidazopyrimidine - Purine - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Fluorobenzene - Halobenzene - Ketal - Pyrimidone - Alkylarylsilane - Benzenoid - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Pyrimidine - Piperidine - Monosaccharide - N-substituted imidazole - Vinylogous amide - Azole - Heteroaromatic compound - Imidazole - Oxolane - Silyl ether - Tertiary amine - Secondary alcohol - Organic metalloid salt - Azacycle - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Oxacycle - Amidine - Carboxylic acid amidine - Formamidine - Acetal - Organoheterosilane - Organic oxygen compound - Organic nitrogen compound - Organosilicon compound - Organopnictogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Amine - Organohalogen compound - Organic metalloid moeity - Organofluoride - 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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