Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](OCC2=CN(CC3=C(CN4C=C(CO[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)N=N4)C(CN4C=C(CO[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)N=N4)=C(CN4C=C(CO[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)N=N4)C(CN4C=C(CO[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)N=N4)=C3CN3C=C(CO[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)N=N3)N=N2)[C@@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=HYHDQHGODVNHDE-SNTQDKTISA-N

Formula

C66H96N18O36

Mass

1717.584

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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

O-glycosyl compounds

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

O-glycosyl compound - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Azole - Heteroaromatic compound - 1,2,3-triazole - Secondary alcohol - Acetal - Oxacycle - Azacycle - Polyol - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Primary alcohol - Organopnictogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

External Descriptors

Not available

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