Compound Identification
SMILES
COC1=C(O)C=C(CN(CCC2=CC(Br)=C(O)C=C2)C=O)C(Br)=C1
InChIKey
InChIKey=CKEYUZMSEQUVIP-UHFFFAOYSA-N
Formula
C17H17Br2NO4
Mass
459.134
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Amaryllidaceae alkaloids
Subclass
Norbelladine-type amaryllidaceae alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Norbelladine-type amaryllidaceae alkaloids
Alternative Parents
Methoxyphenols Anisoles Phenoxy compounds P-bromophenols Methoxybenzenes O-bromophenols 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Bromobenzenes Aryl bromides Tertiary carboxylic acid amides Hydrocarbon derivatives Carbonyl compounds Organonitrogen compounds Organobromides Organic oxides
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Norbelladine skeleton - Methoxyphenol - Phenoxy compound - Anisole - 2-halophenol - Methoxybenzene - 2-bromophenol - 4-halophenol - Phenol ether - 4-bromophenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Halobenzene - Bromobenzene - Aryl bromide - Monocyclic benzene moiety - Benzenoid - Aryl halide - Tertiary carboxylic acid amide - Carboxamide group - Ether - Carboxylic acid derivative - Organobromide - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as norbelladine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids compounds containing the norbelladine skeleton. They are derived initially from the condensation of tyramine and protocatechuic aldehyde or its derivatives in plants.
External Descriptors
Not available