Compound Identification
SMILES
COC1=C(OCC2=CC=CC=C2)C=C(C[C@@H]([C@@H](CC2=C(C)C(O[Si](C)(C)C(C)(C)C)=C(OC)C=C2C)O[Si](C)(C)C(C)(C)C)[N+]([O-])=O)C=C1
InChIKey
InChIKey=KNPGENDJXVSVFA-UZNNEEJFSA-N
Formula
C39H59NO7Si2
Mass
710.071
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Lignans, neolignans and related compounds
Kingdom
Organic compounds
Superclass
Lignans, neolignans and related compounds
Class
Not available
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Lignans, neolignans and related compounds
Alternative Parents
Amphetamines and derivatives m-Xylenes Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Trialkylheterosilanes Silyl ethers C-nitro compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic metalloid salts Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic zwitterions
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Norlignan skeleton - Amphetamine or derivatives - Phenol ether - Methoxybenzene - Xylene - M-xylene - Anisole - Phenoxy compound - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Trialkylheterosilane - Organic nitro compound - C-nitro compound - Silyl ether - Organic oxoazanium - Organic metalloid salt - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organoheterosilane - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic metalloid moeity - Organosilicon compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.
External Descriptors
Not available