Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1CC(=O)[C@@H](CC(=O)OCC(=O)NC2=CC(C)=C(C)C=C2)[C@H]1C[N+]([O-])=O

InChIKey

InChIKey=LLSGMLPDLGNXQI-KBMXLJTQSA-N

Formula

C19H24N2O6

Mass

376.409

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Monoterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Iridoids and derivatives

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Aromatic monoterpenoid - 11-noriridane monoterpenoid - Monocyclic monoterpenoid - Anilide - N-arylamide - O-xylene - Xylene - Monocyclic benzene moiety - Benzenoid - Organic nitro compound - Carboxamide group - Carboxylic acid ester - Ketone - C-nitro compound - Cyclic ketone - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic salt - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic cation - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

External Descriptors

Not available

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