Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1C[C@H](O[13C@@H]2C3=[13C](O)C4=[13C](C(O)=[13C]3O[C@@]22OC3=[13C](C[13C@H]2O)C=[13C]2C=[13C](O[13C](=O)C2=[13C]3O)C(=O)OC)C(=O)[13C](OC)=C[13C]4=O)O[C@@H](C)[C@@H]1O

InChIKey

InChIKey=MLFZQFHGXSVTGX-UVXCSRACSA-N

Formula

C33H30O17

Mass

710.494

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Benzopyrans

Subclass

1-benzopyrans

Intermediate Tree Nodes

Not available

Direct Parent

Pyranochromenes

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranochromene - Naphthofuran - Hexose monosaccharide - Naphthoquinone - Glycosyl compound - Isocoumarin - O-glycosyl compound - Naphthalene - 2-benzopyran - Coumaran - Quinone - Aryl ketone - Pyranone - 1-hydroxy-4-unsubstituted benzenoid - Ketal - Benzenoid - Pyran - Oxane - Monosaccharide - Vinylogous acid - Methyl ester - Vinylogous ester - Heteroaromatic compound - Secondary alcohol - Carboxylic acid ester - Ketone - Lactone - Acetal - Carboxylic acid derivative - Polyol - Dialkyl ether - Ether - Oxacycle - Monocarboxylic acid or derivatives - Alcohol - Organooxygen compound - Organic oxygen compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyranochromenes. These are organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.

External Descriptors

Not available

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