Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CN(O)N=NC2=CC=C(C=C2)[N+]([O-])=O)O[C@H]([C@@H]1O[Si](C)(C)C(C)(C)C)N1C=CC(=O)NC1=O

InChIKey

InChIKey=WYJIMXOFHSOWNJ-MSNJVRRCSA-N

Formula

C27H44N6O8Si2

Mass

636.853

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Nitrobenzene - Nitroaromatic compound - Pyrimidone - Benzenoid - Monocyclic benzene moiety - Pyrimidine - Monosaccharide - Hydropyrimidine - Trialkylheterosilane - Oxolane - Heteroaromatic compound - Vinylogous amide - Organic nitro compound - Urea - C-nitro compound - Silyl ether - Lactam - Organoheterosilane - Oxacycle - Azacycle - N-organohydroxylamine - Organic oxoazanium - Organic metalloid salt - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Organic oxygen compound - Organosilicon compound - Organic zwitterion - Organic metalloid moeity - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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