Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)N1C=NC2=C1N=C(F)N=C2Cl

InChIKey

InChIKey=INSVXRDOQFLRTH-UMCMBGNQSA-N

Formula

C28H52ClFN4O4Si3

Mass

647.45

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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 - N-glycosyl compound - Glycosyl compound - Purine - Imidazopyrimidine - 2-halopyrimidine - Halopyrimidine - Aryl halide - Monosaccharide - N-substituted imidazole - Pyrimidine - Aryl fluoride - Aryl chloride - Trialkylheterosilane - Imidazole - Oxolane - Heteroaromatic compound - Azole - Silyl ether - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organooxygen compound - Organosilicon compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organohalogen compound - Organic metalloid moeity - Organochloride - Organofluoride - 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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