Structure Information
Structure

Compound Identification

SMILES

COC(=O)[C@H](CCCCN)N=C(O)[C@H](CC1=CC=C(O)C=C1)NC(=O)C1=CC=C(C=C1)C1=C2C=CC(=N2)C(=C2NC(C=C2)=C(C2=NC(C=C2)=C(C2=CC=C1N2)C1=CC=C(C=C1)C(=O)N[C@@H](CCCCN)C(O)=NCCCCCN)C1=CC=C(C=C1)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=N[C@@H](CCCCN)C(=O)OC)C1=CC=C(C=C1)C(=O)N[C@@H](CCCCN)C(O)=NCCCCCN

InChIKey

InChIKey=OIGDZNFLQYPANR-IGTRIQHTSA-N

Formula

C102H124N18O14

Mass

1826.226

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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 - Alpha peptide - Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Amphetamine or derivatives - Benzamide - Benzoic acid or derivatives - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Fatty acid ester - Phenol - Dicarboxylic acid or derivatives - Fatty acyl - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Methyl ester - Pyrrole - Amino acid or derivatives - Carboxylic acid ester - Carboxamide group - Secondary carboxylic acid amide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - 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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