Compound Identification
SMILES
OC[C@H](CC1=CC=CC=C1)NC1=NC(=NC2=C1N=CN2[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)C1=CC(CO)=NO1)N1CC[C@H](C1)NC(=O)NC1=CN=CC=C1
InChIKey
InChIKey=SUKNWPHRFRXRFU-FZCPYLNPSA-N
Formula
C32H36N10O7
Mass
672.703
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
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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
6-alkylaminopurines Amphetamines and derivatives Dialkylarylamines Aminopyrimidines and derivatives Pyridines and derivatives N-substituted imidazoles Imidolactams Pyrrolidines Oxolanes Isoxazoles Heteroaromatic compounds Ureas Secondary alcohols Oxacyclic compounds Azacyclic compounds Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Amphetamine or derivatives - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Pyridine - Pyrimidine - Benzenoid - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Isoxazole - Oxolane - Pyrrolidine - Urea - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Alcohol - Aromatic alcohol - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Primary alcohol - Amine - Organic oxide - 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