Compound Identification
SMILES
CN1C(=O)N(C=C(C)C1=O)[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)C2(OS(=O)(=O)C=C2)[C@H]1O[Si](C(C)(C)C)(C(C)(C)C)C(C)(C)C
InChIKey
InChIKey=ZSRKWZQWYLRZEE-MMKNTUCFSA-N
Formula
C31H56N2O8SSi2
Mass
673.03
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 Hydropyrimidines Monosaccharides Organosulfonic acid esters Sulfonic acid esters Vinylogous amides Oxolanes Oxathioles Heteroaromatic compounds Trialkylheterosilanes Lactams Silyl ethers Ureas Oxacyclic compounds Organic metalloid salts Azacyclic compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Sulfonic acid ester - Organosulfonic acid ester - Trialkylheterosilane - 1,2-oxathiole - Oxolane - Organic sulfonic acid or derivatives - Heteroaromatic compound - Organosulfonic acid or derivatives - Vinylogous amide - Lactam - Urea - Silyl ether - Oxacycle - Organoheterosilane - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Organic metalloid moeity - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organosilicon compound - Organonitrogen 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