Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@H](O)[C@@H](COP(=O)(NCCCN(C)C)O[C@H]2C[C@@H](O[C@@H]2CO)N2C=NC3=C2NC(N)=NC3=O)O[C@H]1N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=XCYQDMPSBPYXIY-NQEQPODVSA-N

Formula

C26H39N12O9P

Mass

694.647

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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-aminopurine - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Phosphoric diester monoamide - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Organic phosphoric acid derivative - Monosaccharide - Phosphoric acid ester - Imidolactam - Pyrimidine - Organic phosphoric acid amide - Azole - Oxolane - Imidazole - Heteroaromatic compound - Vinylogous amide - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Oxacycle - Amine - Alcohol - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organic nitrogen compound - 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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