Compound Identification
SMILES
CNC1=NC(=O)N(C=C1)[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@]2(OS(=O)(=O)C=C2N)[C@H]1O[Si](C)(C)C(C)(C)C
InChIKey
InChIKey=KRASIMOWYZZCQK-SSYAZSBWSA-N
Formula
C24H44N4O7SSi2
Mass
588.87
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Glycosylamines
-
Level 5
Glycosyl compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
Glycosylamines
Alternative Parents
Pyrimidones Aminopyrimidines and derivatives Sulfonic acid esters Organosulfonic acid esters Hydropyrimidines Monosaccharides Imidolactams Trialkylheterosilanes Oxolanes Oxathioles Heteroaromatic compounds Silyl ethers Oxacyclic compounds Azacyclic compounds Enamines Organic metalloid salts Hydrocarbon derivatives Organic oxides Monoalkylamines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Organosulfonic acid ester - Sulfonic acid ester - Trialkylheterosilane - Heteroaromatic compound - 1,2-oxathiole - Oxolane - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Silyl ether - Enamine - Organoheterosilane - Oxacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organonitrogen compound - Organic metalloid moeity - Hydrocarbon derivative - Primary aliphatic amine - Amine - Primary amine - Organic nitrogen compound - Organic oxide - Organosilicon compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).
External Descriptors
Not available