Compound Identification
SMILES
CCOP(=O)(CCN1C[C@@H](O)[C@H](O)C1)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O
InChIKey
InChIKey=VMUGQFRHAAEKSX-JNVRCDIISA-N
Formula
C17H28N3O10P
Mass
465.396
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Glycosyl compounds
- Level 6 Glycosylamines
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Level 5
Glycosyl compounds
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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
Pentoses Dialkyl alkylphosphonates Pyrimidones Hydropyrimidines Phosphonic acid esters N-alkylpyrrolidines Vinylogous amides Heteroaromatic compounds Oxolanes Ureas Trialkylamines 1,2-aminoalcohols 1,2-diols Lactams Secondary alcohols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic oxides Organophosphorus compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N-glycosyl compound - Pentose monosaccharide - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Hydropyrimidine - Monosaccharide - N-alkylpyrrolidine - Phosphonic acid ester - Pyrimidine - Heteroaromatic compound - Organophosphonic acid derivative - Vinylogous amide - Oxolane - Pyrrolidine - Lactam - Urea - 1,2-aminoalcohol - Tertiary aliphatic amine - Tertiary amine - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Alcohol - Organic oxide - Organophosphorus compound - Hydrocarbon derivative - Amine - Organic nitrogen compound - Aromatic heteromonocyclic 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