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@H](SC(=O)C3=C(C)C(I)=C(O[C@@H]4O[C@@H](C)[C@H](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#C[C@@]2(O)CC(=O)C(NC(=O)OC)=C1\C2=C/CSSSC
InChIKey
InChIKey=HXCHCVDVKSCDHU-SNTWSMTASA-N
Formula
C55H74IN3O21S4
Mass
1368.34
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 Cyclohexenones Toluenes Iodobenzenes Oxanes Ynones Aryl iodides Monosaccharides Tertiary alcohols Organic trisulfides Methylcarbamates Secondary alcohols Carbothioic S-esters Organic carbonic acids and derivatives Thioesters Dialkylamines Dialkyl ethers Sulfenyl compounds Acetals Oxacyclic compounds N-organohydroxylamines Organic oxides Organoiodides Hydrocarbon derivatives 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 - Halobenzene - Alkyl aryl ether - Iodobenzene - Aryl halide - Aryl iodide - 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 - Dialkyl ether - N-organohydroxylamine - Carboxylic acid derivative - Thiocarboxylic acid or derivatives - Secondary aliphatic amine - Secondary amine - Ether - Acetal - Sulfenyl compound - Oxacycle - Organoheterocyclic compound - Organosulfur compound - Organic oxide - Organopnictogen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Amine - Organohalogen compound - Organoiodide - 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