Compound Identification
SMILES
CCN1CCN(CC1)C(=O)C1=CSC(CN(CCC2=CC(OC)=C(OC)C=C2)CC2=CC=C(OCC3=CC=CC=C3)C=C2)=N1
InChIKey
InChIKey=SOENFJAHEGMSRB-UHFFFAOYSA-N
Formula
C35H42N4O4S
Mass
614.81
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
Dimethoxybenzenes Phenethylamines 2-heteroaryl carboxamides Anisoles Benzylamines Thiazolecarboxamides Phenoxy compounds Phenylmethylamines Alkyl aryl ethers N-alkylpiperazines 2,4-disubstituted thiazoles Aralkylamines Heteroaromatic compounds Tertiary carboxylic acid amides Trialkylamines Amino acids and derivatives Azacyclic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Norbelladine skeleton - O-dimethoxybenzene - Dimethoxybenzene - Phenethylamine - 2-heteroaryl carboxamide - Thiazolecarboxamide - Phenoxy compound - Thiazolecarboxylic acid or derivatives - Anisole - Phenylmethylamine - Benzylamine - Phenol ether - Methoxybenzene - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - N-alkylpiperazine - Aralkylamine - 1,4-diazinane - Piperazine - Benzenoid - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Thiazole - Tertiary carboxylic acid amide - Carboxamide group - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Organoheterocyclic compound - Ether - Azacycle - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Amine - Aromatic heteromonocyclic 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