Structure Information
Structure

Compound Identification

SMILES

[NH-]C1C(O)C(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(O)C(O)C6[NH-])C(O)C(O)C5[NH-])C(O)C(O)C4[NH-])C(O)C(O)C3[NH-])C(O)C(O)C2[NH-])O[C@H]1CO

InChIKey

InChIKey=OQANUBRXSOQJOA-CDHUKCIOSA-N

Formula

C42H79N6O40P5

Mass

1462.968

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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 - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Alkyl phosphate - Secondary alcohol - Oxacycle - Ether - Dialkyl ether - Organoheterocyclic compound - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic anion - 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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