Compound Identification
SMILES
CCCCCCCCCCCCN1C=CC(C=C1)=C(O)NC1=CC=C(C=C1)C1=C2C=CC(=N2)C(=C2C=CC(=N2)C(=C2C=CC(=N2)C(=C2C=CC1=N2)C1=CC=C(NC(=O)C2=CC=[N+](CCCCCCCCCCCC)C=C2)C=C1)C1=CC=C(NC(=O)C2=CC=[N+](CCCCCCCCCCCC)C=C2)C=C1)C1=CC=C(NC(=O)C2=CC=[N+](CCCCCCCCCCCC)C=C2)C=C1
InChIKey
InChIKey=XVYPEORDNAFJDG-UHFFFAOYSA-Q
Formula
C116H145N12O4
Mass
1771.514
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Tetrapyrroles and derivatives
- Subclass Porphyrins
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Class
Tetrapyrroles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Tetrapyrroles and derivatives
Subclass
Porphyrins
Intermediate Tree Nodes
Not available
Direct Parent
Porphyrins
Alternative Parents
Aromatic anilides Pyridinecarboxylic acids and derivatives Dihydropyridines Pyridinium derivatives Pyrroles Heteroaromatic compounds Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Ketene acetals Alkanolamines Allylamines Azacyclic compounds Enamines Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Porphyrin - Aromatic anilide - Pyridine carboxylic acid or derivatives - Dihydropyridine - Monocyclic benzene moiety - Hydropyridine - Pyridine - Pyridinium - Benzenoid - Pyrrole - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Ketene acetal or derivatives - Allylamine - Azacycle - Alkanolamine - Carboxylic acid derivative - Enamine - Hydrocarbon derivative - Organic oxide - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic cation - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as porphyrins. These are compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure.
External Descriptors
Not available