Compound Identification
SMILES
C[C@@H]1CC[C@H]2[C@@H](C)[C@@H](OCCCCCCCCCCOC(=O)CCC(O)=O)O[C@@H]3O[C@@]4(C)CC[C@@H]1[C@@]23OO4
InChIKey
InChIKey=OOLUMZMWJKYDTC-WNBMRRHZSA-N
Formula
C29H48O9
Mass
540.694
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Sesquiterpenoids
- Level 5 Artemisinins
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Subclass
Sesquiterpenoids
-
Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Sesquiterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Artemisinins
Alternative Parents
Oxepanes Heterocyclic fatty acids Fatty acid esters Trioxanes Oxanes Dicarboxylic acids and derivatives Dialkyl peroxides Carboxylic acid esters Oxacyclic compounds Carboxylic acids Acetals Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Artemisinin skeleton - Fatty acid ester - Heterocyclic fatty acid - Oxepane - Dicarboxylic acid or derivatives - Oxane - Fatty acyl - 1,2,4-trioxane - Carboxylic acid ester - Dialkyl peroxide - Oxacycle - Carboxylic acid - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as artemisinins. These are sesquiterpenoids originally isolated from the herb Artemisia annua. Their structure is based on artemisinin, a tetracyclic compound that contains a 1,2-dioxepane fused to an octahydrobenzopyran moiety. The internal peroxide bridge is believed to be a key to the mode of action of artemisinins.
External Descriptors
Not available