Compound Identification
SMILES
COC(=O)CC1C(C)(C)C(=O)C2CC3=C4CC(=O)OC(C5=COC=C5)C4(C)CCC3C1(C)C2=O
InChIKey
InChIKey=DNFJSIPZGYBGON-UHFFFAOYSA-N
Formula
C27H32O7
Mass
468.546
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Triterpenoids
- Level 5 Limonoids
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Subclass
Triterpenoids
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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
Triterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Limonoids
Alternative Parents
Naphthopyrans Naphthalenes Delta valerolactones Beta-diketones Pyrans Oxanes Dicarboxylic acids and derivatives Methyl esters Heteroaromatic compounds Furans Ketones Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Limonoid skeleton - Mexicanolide - Naphthopyran - Naphthalene - Delta valerolactone - Delta_valerolactone - 1,3-diketone - Dicarboxylic acid or derivatives - 1,3-dicarbonyl compound - Pyran - Oxane - Furan - Heteroaromatic compound - Methyl ester - Lactone - Ketone - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.
External Descriptors
Not available