Structure Information
Structure

Compound Identification

SMILES

CCC1(CC)[C@H](C)\C(=C\C)C2=C3N1C[C@H]1O[C@H]([C@H](O[Si](C)(C)C(C)(C)C)[C@@]31OS2(=O)=O)N1C=C(C)C(=O)NC1=O

InChIKey

InChIKey=HQCFULRHYXBAAH-GTGAYRQTSA-N

Formula

C28H43N3O7SSi

Mass

593.81

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

N-glycosyl compound - Furopyrrole - Pyrimidone - Tetrahydropyridine - Hydropyrimidine - Monosaccharide - Pyrimidine - Sulfonic acid ester - Organosulfonic acid ester - N-alkylpyrrolidine - Furan - Trialkylheterosilane - 1,2-oxathiole - Oxolane - Heteroaromatic compound - Pyrrole - Pyrrolidine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Vinylogous amide - Lactam - Silyl ether - Urea - Tertiary aliphatic amine - Tertiary amine - Oxacycle - Organoheterosilane - Organoheterocyclic compound - Enamine - Organic metalloid salt - Azacycle - Organic metalloid moeity - Organic oxide - Organonitrogen compound - Amine - Hydrocarbon derivative - Organosilicon compound - Organic nitrogen 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

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