Compound Identification
SMILES
CCN[C@H]1CO[C@H](C[C@@H]1OC)O[C@@H]1[C@@H](O)[C@H](NO[C@H]2C[C@H](O)C(SC(=O)C3=C(C)C(Br)=C(O[C@@H]4O[C@@H](C)C(O)[C@@H](OC)[C@H]4O)C(OC)=C3OC)[C@@H](C)O2)[C@@H](C)O[C@H]1O[C@H]1C#C\C=C/C#CC2(O)CC(=O)C(NC(=O)OC)=C1\C2=C/CSC(C)=O
InChIKey
InChIKey=RKRBFCZGVGVDEA-WNEFSKBWSA-N
Formula
C56H74BrN3O22S2
Mass
1285.23
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
-
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-glycosyl compounds 3-halobenzoic acids and derivatives Dimethoxybenzenes Thiobenzoic acids and derivatives Anisoles Benzoyl derivatives Phenoxy compounds Toluenes Alkyl aryl ethers Bromobenzenes Cyclohexenones Ynones Aryl bromides Oxanes Monosaccharides Methylcarbamates Tertiary alcohols Thioesters Carbothioic S-esters Secondary alcohols Oxacyclic compounds Dialkylamines Dialkyl ethers Sulfenyl compounds Acetals N-organohydroxylamines Hydrocarbon derivatives Aldehydes Organopnictogen compounds Organic oxides Organobromides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - O-glycosyl compound - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Dimethoxybenzene - O-dimethoxybenzene - Thiobenzoic acid or derivatives - Benzoic acid or derivatives - Phenol ether - Methoxybenzene - Phenoxy compound - Anisole - Benzoyl - Toluene - Alkyl aryl ether - Halobenzene - Bromobenzene - Cyclohexenone - Aryl bromide - Oxane - Monosaccharide - Aryl halide - Benzenoid - Ynone - Monocyclic benzene moiety - Methylcarbamate - Carbamic acid ester - Tertiary alcohol - Amino acid or derivatives - Carbothioic s-ester - Cyclic ketone - Ketone - Thiocarboxylic acid ester - Secondary alcohol - Acetal - Secondary amine - Thiocarboxylic acid or derivatives - Oxacycle - N-organohydroxylamine - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Sulfenyl compound - Organobromide - Organonitrogen compound - Alcohol - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aldehyde - Organic nitrogen compound - Organosulfur compound - Amine - Organohalogen compound - 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