Structure Information
Structure

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

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Subclass

Porphyrins

Intermediate Tree Nodes

Not available

Direct Parent

Porphyrins

Alternative Parents

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

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