Compound Identification
SMILES
CCCC(=O)C1=C(O)C([C@H]2C=C3CCC[C@@H](C)[C@]3(C)[C@H]3[C@@H]2C3(C)C)=C(O)C(CC2=C(O)C(C)(C)C(=O)C(C(C)=O)=C2O)=C1O
InChIKey
InChIKey=YJNHLYUPQQDOHX-MOBFWXDPSA-N
Formula
C36H46O8
Mass
606.756
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Lipids and lipid-like molecules
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Class
Prenol lipids
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Subclass
Sesquiterpenoids
- Level 5 Aristolane sesquiterpenoids
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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
Aristolane sesquiterpenoids
Alternative Parents
Alkyl-phenylketones Butyrophenones Acylphloroglucinols and derivatives Benzoyl derivatives Aryl alkyl ketones Vinylogous acids Cyclic ketones Polyols Enols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Aristolane sesquiterpenoid - Alkyl-phenylketone - Acylphloroglucinol derivative - Butyrophenone - Phenylketone - Benzenetriol - Phloroglucinol derivative - Aryl alkyl ketone - Aryl ketone - Benzoyl - Phenol - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Cyclic ketone - Ketone - Polyol - Enol - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as aristolane sesquiterpenoids. These are sesquiterpenoids with a structure based on the aristolane skeleton. Aristolanes arise from the C6,C11 cyclization of the bicyclic eremophilane skeleton.
External Descriptors
Not available