Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](SCCOCCOC2=CC=C(C=C2)C2=C3NC(C=C3)=C(C3=CC=C(N3)C(=C3C=CC(=N3)C(=C3C=CC2=N3)C2=CC=C(OCCOCCS[C@@H]3O[C@H](CO)[C@H](O)[C@@H](O)[C@H]3O)C=C2)C2=CC=C(OCCOCCS[C@@H]3O[C@H](CO)[C@H](O)[C@@H](O)[C@H]3O)C=C2)C2=CC=CC=C2)[C@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=DLBDPOGAWVBXIE-QKVBWJDKSA-N

Formula

C74H84N4O21S3

Mass

1461.67

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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 - Glycosyl compound - S-glycosyl compound - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Pyrrole - Heteroaromatic compound - Monothioacetal - Secondary alcohol - 1,2-diol - Azacycle - Sulfenyl compound - Oxacycle - Dialkyl ether - Ether - Polyol - Alcohol - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - 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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