Compound Identification
SMILES
[2H]C([2H])(OC1=CC=C(C=C1)C(=O)C1=C(SC2=C1C=CC(O[C@@H]1OC([C@@H](O)[C@H](O)[C@@H]1O)C(O)=O)=C2)C1=CC=C(O)C=C1)C([2H])([2H])N1CCCCC1
InChIKey
InChIKey=MZPMSLSINDGEPM-YLCXKQQRSA-N
Formula
C34H35NO10S
Mass
653.74
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
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Subclass
Carbohydrates and carbohydrate conjugates
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Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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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
Phenolic glycosides
Alternative Parents
O-glucuronides Aryl-phenylketones 3-aroylthiophenes O-glycosyl compounds 1-benzothiophenes Thiophene carboxylic acids and derivatives Benzoyl derivatives Phenol ethers Phenoxy compounds Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Beta hydroxy acids and derivatives Pyrans Monosaccharides Piperidines Oxanes Heteroaromatic compounds Trialkylamines Secondary alcohols Amino acids Polyols Monocarboxylic acids and derivatives Oxacyclic compounds Carboxylic acids Acetals Azacyclic compounds Aldehydes Organic oxides Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Aryl-phenylketone - 3-aroylthiophene - O-glycosyl compound - 1-benzothiophene - Benzothiophene - Phenoxy compound - Phenol ether - Thiophene carboxylic acid or derivatives - Aryl ketone - Benzoyl - Beta-hydroxy acid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Benzenoid - Oxane - Monosaccharide - Piperidine - Hydroxy acid - Pyran - Monocyclic benzene moiety - Heteroaromatic compound - Thiophene - Tertiary aliphatic amine - Amino acid - Amino acid or derivatives - Secondary alcohol - Tertiary amine - Ketone - Acetal - Oxacycle - Azacycle - Carboxylic acid derivative - Carboxylic acid - Ether - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Alcohol - Aldehyde - Carbonyl group - Organic nitrogen compound - Amine - Organopnictogen compound - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
External Descriptors
Not available