Structure Information
Structure

Compound Identification

SMILES

C\C(\C=C\CC(C)(C)OC1OC(CO)C(O)C(O)C1O)=C/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(C)C(=O)CCC1(C)C

InChIKey

InChIKey=ALUKCTZWAURVJZ-SORTXIFMSA-N

Formula

C46H64O7

Mass

729.011

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Tetraterpenoids

Intermediate Tree Nodes

Carotenoids

Direct Parent

Xanthophylls

Alternative Parents

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Xanthophyll - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Cyclohexenone - Fatty acyl - Monosaccharide - Oxane - Ketone - Secondary alcohol - Cyclic ketone - Polyol - Organoheterocyclic compound - Acetal - Oxacycle - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Primary alcohol - Aliphatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as xanthophylls. These are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone.

External Descriptors

Not available

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