Compound Identification
SMILES
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O
InChIKey
InChIKey=FQURJFMVIDBLGD-OJAKKHQRSA-N
Formula
C15H27N3O5Si
Mass
357.482
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Pyrimidine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Pyrimidine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Pyrimidine nucleosides
Alternative Parents
Glycosylamines Pentoses Pyrimidones Aminopyrimidines and derivatives Imidolactams Hydropyrimidines Trialkylheterosilanes Oxolanes Heteroaromatic compounds Silyl ethers Secondary alcohols 1,2-diols Oxacyclic compounds Organic metalloid salts Azacyclic compounds Hydrocarbon derivatives Organic oxides Primary amines
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Heteroaromatic compound - Trialkylheterosilane - Oxolane - Silyl ether - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic metalloid salt - Organoheterosilane - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Alcohol - Primary amine - Organic oxide - Organic oxygen compound - Amine - Hydrocarbon derivative - Organosilicon compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrimidine nucleosides. These are compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available