Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](OC[C@H]1S[C@H]([C@@H](F)[C@@H]1OCC1=CC=CC=C1)N1C=NC2=C1N=C(N)N=C2N)(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=RFKYJLZCZAPOCQ-IWQUTFRXSA-N

Formula

C33H37FN6O2SSi

Mass

628.84

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Thionucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Thionucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine thionucleoside - 6-aminopurine - Benzylether - Purine - Imidazopyrimidine - Aminopyrimidine - Alkylarylsilane - Pyrimidine - Monocyclic benzene moiety - Imidolactam - N-substituted imidazole - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Thiolane - Silyl ether - Organoheterosilane - Azacycle - Dialkyl ether - Ether - Organic metalloid salt - Organoheterocyclic compound - Dialkylthioether - Thioether - Organic nitrogen compound - Organic oxygen compound - Amine - Alkyl halide - Alkyl fluoride - Organohalogen compound - Organic metalloid moeity - Organofluoride - Organonitrogen compound - Organooxygen compound - Primary amine - Organosilicon compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as thionucleosides. These are nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.

External Descriptors

Not available

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