Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CO[C@@H]2[C@@H](C)[C@@H]3O[C@H](CCO[Si](C4=CC=CC=C4)(C4=CC=CC=C4)C(C)(C)C)[C@@H](C[C@@H]3O[C@H]2C[C@@H](O)C(=C)[C@H](C)C\C=C(/C[C@@H]2O[C@@H](CCCOC(=O)C(C)(C)C)CC2=C)C(=O)O[C@H]2[C@H](SC3=CC=CC=C3)C3=CC=CC=C3C3=CC=CC=C23)O[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)C=C1

InChIKey

InChIKey=DVTAKAQDCJRWMQ-MULMDQRTSA-N

Formula

C95H114O12SSi2

Mass

1536.18

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Terpene glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Terpene glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Terpene glycoside - Phenanthrene - Hydrophenanthrene - Glycosyl compound - C-glycosyl compound - Monoterpenoid - Naphthalene - Aromatic monoterpenoid - Benzylether - Thiophenol ether - Methoxybenzene - Aryl thioether - Phenol ether - Phenoxy compound - Anisole - Fatty acid ester - Alkylarylsilane - Alkyl aryl ether - Alkylarylthioether - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Fatty acyl - Monosaccharide - Benzenoid - Oxane - Oxolane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Silyl ether - Secondary alcohol - Carboxylic acid ester - Thioether - Sulfenyl compound - Oxacycle - Organoheterocyclic compound - Organoheterosilane - Organic metalloid salt - Ether - Carboxylic acid derivative - Dialkyl ether - Organosilicon compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic metalloid moeity - Organooxygen compound - Organosulfur compound - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

External Descriptors

Not available

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