Compound Identification
SMILES
CC1=CN([C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C(=O)NC1=O
InChIKey
InChIKey=ZJRRJBUBDBSBRI-HKUMRIAESA-N
Formula
C16H28N2O6Si
Mass
372.493
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 Hydropyrimidines Vinylogous amides Trialkylheterosilanes Oxolanes Heteroaromatic compounds Ureas Silyl ethers Secondary alcohols 1,2-diols Lactams Oxacyclic compounds Azacyclic compounds Organic metalloid salts Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrimidone - Pyrimidine - Hydropyrimidine - Monosaccharide - Trialkylheterosilane - Vinylogous amide - Heteroaromatic compound - Oxolane - Silyl ether - Secondary alcohol - Lactam - Urea - 1,2-diol - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organonitrogen compound - Organic metalloid moeity - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - 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