Structure Information
Structure

Compound Identification

SMILES

CC[C@H](C)[C@H]1O[C@@]2(C[C@@H]3C[C@@H](C\C=C(C)\[C@@H](O[C@H]4C[C@H](OC)[C@@H](OCOC)[C@H](C)O4)[C@@H](C)\C=C\C=C4/CO[C@@H]5[C@H](O[Si](C)(C)CBr)C(C)=C[C@@H](C(=O)O3)[C@]45O)O2)C=C[C@@H]1C

InChIKey

InChIKey=LHLPFBLUHLBWQP-TVUDEEHTSA-N

Formula

C46H71BrO12Si

Mass

924.051

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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

Aliphatic heteropolycyclic compounds

Substituents

Macrolide - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Ketal - Monosaccharide - Oxane - Pyran - Trialkylheterosilane - Tertiary alcohol - Oxolane - Carboxylic acid ester - Lactone - Silyl ether - Acetal - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterosilane - Oxacycle - Monocarboxylic acid or derivatives - Organic metalloid salt - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Alkyl halide - Alkyl bromide - Carbonyl group - Alcohol - Organic oxygen compound - Organohalogen compound - Organic metalloid moeity - Organobromide - Organooxygen compound - Organosilicon compound - Aliphatic 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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