Structure Information
Structure

Compound Identification

SMILES

C[N+]1=CC=C(C=C1)C1=C2C=CC(=N2)C(=C2NC(C=C2)=C(C2=NC(C=C2)=C(C2=CC=C1N2)C1=CC=[N+](CCCCC(=O)NCCCNCCCCNCCCNC(=O)CCCC[N+]2=CC=C(C=C2)C2=C3C=CC(=N3)C(=C3NC(C=C3)=C(C3=NC(C=C3)=C(C3=CC=C2N3)C2=CC=[N+](C)C=C2)C2=CC=[N+](C)C=C2)C2=CC=[N+](C)C=C2)C=C1)C1=CC=[N+](C)C=C1)C1=CC=[N+](C)C=C1

InChIKey

InChIKey=DWLMIAGVNOFMMA-UHFFFAOYSA-R

Formula

C106H110N20O2

Mass

1696.18

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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 - N-methylpyridinium - Fatty amide - N-acyl-amine - Fatty acyl - Pyridine - Pyridinium - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Secondary aliphatic amine - Azacycle - Secondary amine - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Amine - Organic oxygen compound - Organooxygen compound - Carbonyl group - 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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