Structure Information
Structure

Compound Identification

SMILES

CC1OC(=O)CC2CC(=O)N(CCC3CN(C4=C3C=C(CC3=CC5=C(C=C3)N(CC5CCN3CC5C(C)OC(=O)CC5CC3=O)S(=O)(=O)C(F)(F)F)C=C4)S(=O)(=O)C(F)(F)F)CC12

InChIKey

InChIKey=ATCFRYKEXJDPKB-UHFFFAOYSA-N

Formula

C41H46F6N4O10S2

Mass

932.95

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Alkaloids and derivatives

Class

Yohimbine alkaloids

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Yohimbine alkaloids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Yohimban skeleton - Yohimbine alkaloid - Indole or derivatives - Delta-lactam - Delta valerolactone - Delta_valerolactone - Piperidinone - Dicarboxylic acid or derivatives - Oxane - Piperidine - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Sulfonyl - Tertiary carboxylic acid amide - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Trihalomethane - Lactone - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Organic oxide - Alkyl fluoride - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alkyl halide - Halomethane - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.

External Descriptors

Not available

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