Compound Identification
SMILES
CC(C)[Si](OCC[C@H]1O[C@@H]2OC3(C)CCC4[C@H](C)CCC([C@H]1C)[C@@]24OO3)(OCC[C@H]1O[C@@H]2OC3(C)CCC4[C@H](C)CCC([C@H]1C)[C@@]24OO3)C(C)C
InChIKey
InChIKey=CQHKRBRJWMFKJO-IZPJPVGFSA-N
Formula
C40H68O10Si
Mass
737.059
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
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Class
Prenol lipids
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Subclass
Sesquiterpenoids
- Level 5 Artemisinins
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Subclass
Sesquiterpenoids
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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 Trioxanes Oxanes Alkoxysilanes Silyl ethers Dialkyl peroxides Oxacyclic compounds Organoheterosilanes Organic metalloid salts Acetals Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Artemisinin skeleton - Oxepane - Oxane - 1,2,4-trioxane - Alkoxysilane - Silyl ether - Dialkyl peroxide - Acetal - Organoheterosilane - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organosilicon compound - Organic metalloid moeity - Organooxygen 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