Compound Identification
SMILES
CCC(CC)NC1=NC(NCCC2=CC(OC)=C(OC)C=C2)=NC2=C1N=CN2[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)C1=CC(CC)=NO1
InChIKey
InChIKey=IMMDARQMXLEGDL-XVOBZGQLSA-N
Formula
C29H39N7O6
Mass
581.674
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 Dimethoxybenzenes Phenoxy compounds Anisoles Secondary alkylarylamines Alkyl aryl ethers Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Oxolanes Isoxazoles Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - O-dimethoxybenzene - Dimethoxybenzene - Imidazopyrimidine - Purine - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Heteroaromatic compound - Isoxazole - Azole - Imidazole - Secondary alcohol - 1,2-diol - Secondary amine - Oxacycle - Organoheterocyclic compound - Azacycle - Ether - Organic nitrogen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Alcohol - 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