Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@@H]2C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](CN(O)N=NC3=CC=C(C=C3)[N+]([O-])=O)O2)C(=O)NC1=O

InChIKey

InChIKey=WDYOTQUNDMKOGS-QYZOEREBSA-N

Formula

C22H32N6O7Si

Mass

520.618

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

2',5'-dideoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

2',5'-dideoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

2',5'-dideoxyribonucleoside - Nitrobenzene - Nitroaromatic compound - Pyrimidone - Monocyclic benzene moiety - Hydropyrimidine - Benzenoid - Pyrimidine - Trialkylheterosilane - Vinylogous amide - Oxolane - Heteroaromatic compound - Lactam - Organic nitro compound - C-nitro compound - Silyl ether - Urea - Organoheterosilane - Organic oxoazanium - Oxacycle - Azacycle - N-organohydroxylamine - Organic metalloid salt - Organoheterocyclic compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosilicon compound - Organic metalloid moeity - Organic zwitterion - Organic salt - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as 2',5'-dideoxyribonucleosides. These are nucleosides characterized by a purine or pyrimidine base, which is N-linked to a 2',5'-dideoxyribose moiety.

External Descriptors

Not available

Previous Back Next