Compound Identification
SMILES
O[C@@H]1[C@H](O)[C@H](O[C@H]1N1C=CC(=O)NC1=O)C(=O)N1CCN(CC2=CC=CC=N2)CC1
InChIKey
InChIKey=AQWWCVDCLXZVNX-UIBIWLFHSA-N
Formula
C19H23N5O6
Mass
417.422
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
2-pyridylmethylamines Aralkylamines Pyrimidones N-alkylpiperazines Hydropyrimidines Vinylogous amides Tertiary carboxylic acid amides Heteroaromatic compounds Oxolanes 1,2-diols Ureas Amino acids and derivatives Trialkylamines Secondary alcohols Lactams Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N-glycosyl compound - 2-pyridylmethylamine - Pyrimidone - N-alkylpiperazine - Aralkylamine - 1,4-diazinane - Hydropyrimidine - Piperazine - Pyridine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Oxolane - Tertiary carboxylic acid amide - Urea - Carboxamide group - 1,2-diol - Lactam - Tertiary aliphatic amine - Amino acid or derivatives - Secondary alcohol - Tertiary amine - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Carbonyl group - Organic oxide - 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