Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CC2=C3NC(=C2C=C1C(=O)OC)C(=C1N=C(C2=CC(C(=O)OC)=C(C=C12)C(=O)OC)C(=C1NC(C2=CC(C(=O)OC)=C(C=C12)C(=O)OC)=C(C1=NC(C2=CC(C(=O)OC)=C(C=C12)C(=O)OC)=C3C1=CC=C(C=C1)[N+]([O-])=O)C1=CC=C(C=C1)[N+]([O-])=O)C1=CC=C(C=C1)[N+]([O-])=O)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=YGBRNXDFMWQHIE-UHFFFAOYSA-N

Formula

C76H50N8O24

Mass

1459.268

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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 - Isoindole - Isoindole or derivatives - Nitrobenzene - Nitroaromatic compound - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrrole - Methyl ester - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - 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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