Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@]3(OS(=O)(=O)C=C3N)[C@H]2O[Si](C)(C)C(C)(C)C)C(=O)N(CC#CC2=CN([C@H]3O[C@@H](CO)C=C3)C(=O)NC2=O)C1=O

InChIKey

InChIKey=FWAKNTNQESRKIL-APVLLUGWSA-N

Formula

C36H53N5O12SSi2

Mass

836.07

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Nucleoside and nucleotide analogues

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Sulfonic acid ester - Organosulfonic acid ester - Dihydrofuran - Trialkylheterosilane - Organic sulfonic acid or derivatives - Heteroaromatic compound - 1,2-oxathiole - Oxolane - Vinylogous amide - Organosulfonic acid or derivatives - Urea - Silyl ether - Lactam - Enamine - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Amine - Organic nitrogen compound - Alcohol - Primary alcohol - Primary amine - Organic oxygen compound - Organosilicon compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.

External Descriptors

Not available

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