Compound Identification
SMILES
OC[C@H]1O[C@@H]2O[C@@H]3[C@@H](CO)O[C@H](O[C@@H]4[C@@H](CO)O[C@H](O[C@@H]5[C@@H](CO)O[C@H](O[C@@H]6[C@@H](CNC(=O)C7=CC(=NO7)C7=CC=CC=C7)O[C@H](O[C@@H]7[C@@H](CO)O[C@H](O[C@@H]8[C@@H](CO)O[C@H](O[C@H]1[C@H](O)[C@H]2O)[C@H](O)[C@H]8O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O
InChIKey
InChIKey=QSBIRPOHYBBXBD-VUJXYQPRSA-N
Formula
C52H76N2O36
Mass
1305.158
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
- Level 5 Oligosaccharides
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Not available
Direct Parent
Oligosaccharides
Alternative Parents
2-heteroaryl carboxamides Benzene and substituted derivatives Oxanes Heteroaromatic compounds Isoxazoles Secondary carboxylic acid amides Secondary alcohols Acetals Azacyclic compounds Polyols Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Organopnictogen compounds Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Oligosaccharide - 2-heteroaryl carboxamide - Monocyclic benzene moiety - Oxane - Benzenoid - Azole - Isoxazole - Heteroaromatic compound - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Polyol - Organoheterocyclic compound - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Primary alcohol - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
External Descriptors
Not available