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(OCC(=O)N2CCCCC2)C=CC(Cl)=C1

InChIKey

InChIKey=PMUBSXLLCRCEPC-BINBFKAUSA-N

Formula

C25H31ClN8O5

Mass

559.02

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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

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