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(OC)C=CC(Cl)=C1

InChIKey

InChIKey=OBUJENSIVMMWJQ-OUFKLWKOSA-N

Formula

C19H22ClN7O4

Mass

447.88

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