Compound Identification
SMILES
CC(=O)NC1=C(Cl)C=CC(CO[C@@H]2O[C@H](COCC3=CC=CC=C3)[C@@H](O[C@H]3O[C@@H]4CO[C@H](O[C@H]4[C@H](O)[C@H]3O)C3=CC=CC=C3)[C@H](O)[C@H]2O)=C1
InChIKey
InChIKey=IUQUTXIELGBRCF-JPVNDNJISA-N
Formula
C35H40ClNO12
Mass
702.15
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Glycosyl compounds
- Level 6 O-glycosyl compounds
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Level 5
Glycosyl compounds
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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
Glycosyl compounds
Direct Parent
O-glycosyl compounds
Alternative Parents
O-haloacetanilides Disaccharides Pyranodioxins Benzylethers N-acetylarylamines Chlorobenzenes Oxanes 1,3-dioxanes Aryl chlorides Acetamides Secondary carboxylic acid amides Secondary alcohols Oxacyclic compounds Acetals Dialkyl ethers Organic oxides Organochlorides Carbonyl compounds Hydrocarbon derivatives Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
O-haloacetanilide - Haloacetanilide - Disaccharide - O-glycosyl compound - Acetanilide - Pyranodioxin - N-acetylarylamine - Anilide - Benzylether - N-arylamide - Chlorobenzene - Halobenzene - Meta-dioxane - Aryl chloride - Monocyclic benzene moiety - Aryl halide - Oxane - Benzenoid - Acetamide - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Acetal - Organoheterocyclic compound - Ether - Organic nitrogen compound - Carbonyl group - Organohalogen compound - Organochloride - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Aromatic heteropolycyclic 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