Compound Identification
SMILES
CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O[C@@H]([C@H]1O[Si](C)(C)C(C)(C)C)N1C=CC(=O)NC1=O)\C=N\O
InChIKey
InChIKey=NKQAYPNYSLMYCS-QRTJTOMDSA-N
Formula
C21H39N3O6Si2
Mass
485.728
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class 5'-deoxyribonucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
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
Glycosylamines Pyrimidones Hydropyrimidines Vinylogous amides Trialkylheterosilanes Oxolanes Heteroaromatic compounds Ureas Silyl ethers Aldoximes Lactams Oxacyclic compounds Organic metalloid salts Azacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Pyrimidine - Trialkylheterosilane - Heteroaromatic compound - Oxolane - Vinylogous amide - Aldoxime - Lactam - Urea - Silyl ether - Oxime - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Organoheterosilane - Organic nitrogen compound - Organosilicon compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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