Structure Information
Structure

Compound Identification

SMILES

CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](COP(O)(=O)OC[C@@H]2O[C@H](COP(O)(=O)OC[C@@H]3O[C@H](COP(O)(=O)OC[C@@H]4O[C@H](COP(O)(=O)OC[C@@H]5O[C@H](COP(O)(=O)OC[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@@H](O)[C@H](O)[C@H]5NC(C)=O)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3NC(C)=O)[C@@H](O)[C@H](O)[C@H]2O)O[C@H]1CO

InChIKey

InChIKey=NEZRXFPGGZRKIC-AOHZQNJXSA-N

Formula

C48H88N3O46P5

Mass

1598.076

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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

Not available

Direct Parent

Carbonucleotoids

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Carbonucleotoid backbone - Hexose phosphate - C-glycosyl compound - Glycosyl compound - Monosaccharide phosphate - Dialkyl phosphate - Alkyl phosphate - Phosphoric acid ester - Oxane - Monosaccharide - Organic phosphoric acid derivative - Acetamide - 1,2-diol - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Polyol - Alcohol - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Organonitrogen compound - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as carbonucleotoids. These are organic peptide derivatives with monosaccharide units linked through Phosphate diester bonds.

External Descriptors

Not available

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