Structure Information
Structure

Compound Identification

SMILES

C[C@@]12CC[C@@H]3[C@@]4(C)CCC(=O)C(C)(C)C4=C(O)C(=O)[C@@]3(C)[C@]11O[C@@H]1C[C@H]2C1=COC=C1

InChIKey

InChIKey=JGJQSOSULPIILA-BWLMZZBKSA-N

Formula

C26H32O5

Mass

424.537

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Triterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Limonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Limonoid skeleton - 17-furanylsteroid skeleton - 3-oxo-delta-5-steroid - 7-oxosteroid - Oxosteroid - Delta-5-steroid - Steroid - Naphthopyran - Naphthalene - Cyclohexenone - Pyran - Oxane - Heteroaromatic compound - Furan - Ketone - Cyclic ketone - Dialkyl ether - Enol - Oxirane - Ether - Oxacycle - Organoheterocyclic compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - 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

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