Compound Identification
SMILES
COC1=CC2=C(C=C1)N(C)C(C)=C2C1=CSC(N=C(O)C(C)C2=CC=C(CC(C)C)C=C2)=N1
InChIKey
InChIKey=JGYHMEVFOSFVET-UHFFFAOYSA-N
Formula
C27H31N3O2S
Mass
461.62
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Monoterpenoids
- Level 5 Bicyclic monoterpenoids
-
Subclass
Monoterpenoids
-
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
Bicyclic monoterpenoids
Alternative Parents
N-alkylindoles Aromatic monoterpenoids Phenylpropanes Indoles Anisoles Alkyl aryl ethers 2,4-disubstituted thiazoles N-methylpyrroles Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-alkylindole - Bicyclic monoterpenoid - P-cymene - Aromatic monoterpenoid - Indole or derivatives - Indole - Phenylpropane - Anisole - Phenol ether - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - Benzenoid - Substituted pyrrole - N-methylpyrrole - Monocyclic benzene moiety - Thiazole - Pyrrole - Heteroaromatic compound - Azole - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidic acid - Carboximidic acid derivative - Ether - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
External Descriptors
Not available