Structure Information
Structure

Compound Identification

SMILES

CCCC(=O)N1CCC(CC1)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)C1=CC(=NO1)C(C)(C)C.CC(C)OC(=O)N1CCC(CC1)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)C1=CC(=NO1)C(C)(C)C

InChIKey

InChIKey=HCHOOCGWCZCZIS-ORZVOOTDSA-N

Formula

C50H70N14O11

Mass

1043.197

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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

Not available

Substituents

N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - N-acyl-piperidine - Piperidinecarboxylic acid - Purine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Piperidine - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Isoxazole - Oxolane - Carbamic acid ester - Tertiary carboxylic acid amide - Carboxamide group - Secondary alcohol - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxide - Amine - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - 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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