Compound Identification
SMILES
CC(C)C[C@@H]([C@H]1[C@H](C)C[C@H](NC(C)=O)C1=O)C(=O)N\C(C=O)=C(/C)CCCN=C(N)N
InChIKey
InChIKey=YZKDHRYXGZUGOH-RCQTWUSBSA-N
Formula
C22H37N5O4
Mass
435.569
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Monoterpenoids
- Level 5 Iridoids and derivatives
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Subclass
Monoterpenoids
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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
Monoterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Iridoids and derivatives
Alternative Parents
Monocyclic monoterpenoids N-acyl amines Enals Acetamides Secondary carboxylic acid amides Guanidines Cyclic ketones Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organic oxides Hydrocarbon derivatives Aldehydes
Molecular Framework
Aliphatic homomonocyclic compounds
Substituents
11-noriridane monoterpenoid - Monocyclic monoterpenoid - Fatty amide - Fatty acyl - N-acyl-amine - Alpha,beta-unsaturated aldehyde - Enal - Acetamide - Carboxamide group - Guanidine - Cyclic ketone - Ketone - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Hydrocarbon derivative - Organic oxide - Aldehyde - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Aliphatic 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