Compound Identification
SMILES
CCCCCCCCCCC\C=C\C(=O)OC\C(=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@@]1(O)C(C)=CC(O)CC1(C)C)C(=O)CC1=C(C)C[C@@H](O)CC1(C)C
InChIKey
InChIKey=JNRJSCDJBBSKSU-ZNLKMTGZSA-N
Formula
C54H80O6
Mass
825.228
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
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Subclass
Tetraterpenoids
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Level 5
Carotenoids
- Level 6 Xanthophylls
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Level 5
Carotenoids
-
Subclass
Tetraterpenoids
-
Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Tetraterpenoids
Intermediate Tree Nodes
Carotenoids
Direct Parent
Xanthophylls
Alternative Parents
Fatty alcohol esters Fatty acid esters Alpha-branched alpha,beta-unsaturated ketones Tertiary alcohols Enones Enoate esters Acryloyl compounds Secondary alcohols Ketones Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homomonocyclic compounds
Substituents
Xanthophyll - Fatty alcohol ester - Fatty acid ester - Fatty acyl - Alpha-branched alpha,beta-unsaturated-ketone - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tertiary alcohol - Carboxylic acid ester - Secondary alcohol - Ketone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organooxygen compound - Aliphatic homomonocyclic 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