Structure Information
Structure

Compound Identification

SMILES

CNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1N)N1C=NC2=C1N=CN=C2NCC1=C(OCC2=CC=CO2)C=CC(Cl)=C1

InChIKey

InChIKey=XZNLUSYUSJIGHK-QYUDBREXSA-N

Formula

C23H24ClN7O5

Mass

513.94

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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

Beta amino acid or derivatives - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Benzylamine - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidolactam - Benzenoid - N-substituted imidazole - Pyrimidine - Oxolane - Imidazole - Azole - Furan - Heteroaromatic compound - Secondary alcohol - Amino acid or derivatives - Secondary carboxylic acid amide - 1,2-aminoalcohol - Carboxamide group - Organoheterocyclic compound - Ether - Oxacycle - Azacycle - Carboxylic acid derivative - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organochloride - Organonitrogen compound - Organohalogen compound - Primary amine - Carbonyl group - Primary aliphatic amine - Amine - 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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