Structure Information
Structure

Compound Identification

SMILES

CC(=O)OC[C@H]1O[C@H](O[C@@H]2[C@@H](COC(C)=O)O[C@H]([C@H](OC(C)=O)[C@H]2OC(C)=O)N2C=C(N=N2)C2=CC=C(C=C2)S(N)(=O)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChIKey

InChIKey=ZPJZSTKOPDWFIV-CCHDLNLLSA-N

Formula

C34H42N4O19S

Mass

842.78

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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

Disaccharide - N-glycosyl compound - O-glycosyl compound - Phenyltriazole - Phenyl-1,2,3-triazole - Benzenesulfonamide - Benzenesulfonyl group - Monocyclic benzene moiety - Oxane - Organosulfonic acid amide - Benzenoid - Heteroaromatic compound - Aminosulfonyl compound - 1,2,3-triazole - Triazole - Sulfonyl - Azole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Acetal - Oxacycle - Carboxylic acid derivative - Organosulfur compound - Organopnictogen compound - Organic oxide - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen 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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