Compound Identification
SMILES
CCNC1COC(CC1OC)OC1C(O)C(NOC2CC(O)C(SC(=O)c3c(C)c(Br)c(OC4OC(C)C(O)C(OC)C4O)c(OC)c3OC)C(C)O2)C(C)OC1O[C@@H]1C#C\C=C/C#C[C@]2(O)CC(=O)C(NC(=O)OC)=C1\C2=C\CSSSC
InChIKey
InChIKey=LLGKJKZUFNKSPS-RBNIQKAQSA-N
Formula
C55H74BrN3O21S4
Mass
1321.34
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 Alkyl aryl ethers Bromobenzenes Cyclohexenones Toluenes Oxanes Aryl bromides Ynones Monosaccharides Tertiary alcohols Organic trisulfides Methylcarbamates Secondary alcohols Carbothioic S-esters Organic carbonic acids and derivatives Thioesters Oxacyclic compounds Acetals Dialkylamines Dialkyl ethers Sulfenyl compounds N-organohydroxylamines Hydrocarbon derivatives Organic oxides Organobromides Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - O-glycosyl compound - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Dimethoxybenzene - O-dimethoxybenzene - Thiobenzoic acid or derivatives - Benzoic acid or derivatives - Anisole - Phenoxy compound - Phenol ether - Benzoyl - Methoxybenzene - Toluene - Cyclohexenone - Bromobenzene - Alkyl aryl ether - Halobenzene - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Oxane - Ynone - Benzenoid - Methylcarbamate - Tertiary alcohol - Organic trisulfide - Carbamic acid ester - Ketone - Thiocarboxylic acid ester - Carbonic acid derivative - Carbothioic s-ester - Secondary alcohol - Cyclic ketone - Amino acid or derivatives - Carboxylic acid derivative - N-organohydroxylamine - Acetal - Thiocarboxylic acid or derivatives - Dialkyl ether - Secondary amine - Secondary aliphatic amine - Ether - Sulfenyl compound - Oxacycle - Organoheterocyclic compound - Organosulfur compound - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Amine - Organohalogen compound - Organobromide - Organic nitrogen compound - Organonitrogen 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