Structure Information
Structure

Compound Identification

SMILES

[H][C@](O)(C[C@]1([H])CCC[C@@]([H])(O1)C(C)(C)C(O)=O)C[C@@]1([H])OC(=O)C2=C(CCC[C@@]3([H])CCC[C@@]([H])(CC[C@]([H])(C)[C@@]([H])(C[C@@]([H])(O)C[C@]4([H])CCC[C@@]([H])(O4)C(C)(C)C(O)=O)OC(=O)C4=C(CCC[C@@]5([H])CCC[C@@]([H])(CC[C@]1([H])C)O5)C=CC=C4[O-])O3)C=CC=C2O

InChIKey

InChIKey=CLRJANNDAMZRHN-NDUBEVKVSA-M

Formula

C64H95O16

Mass

1120.449

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolides and analogues

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macrolide - Tetracarboxylic acid or derivatives - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenoxide - Oxane - Benzenoid - Vinylogous acid - Carboxylic acid ester - Lactone - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

External Descriptors

Not available

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