Structure Information
Structure

Compound Identification

SMILES

CC1OC(=O)CC2CC(=O)N(CCC3CN(C4=CC=CC=C34)S(=O)(=O)C(F)(F)F)CC12

InChIKey

InChIKey=PGMSSMPOZWHEEP-UHFFFAOYSA-N

Formula

C20H23F3N2O5S

Mass

460.47

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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 - Oxane - Piperidine - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Tertiary carboxylic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxamide group - Carboxylic acid ester - Lactam - Trihalomethane - Lactone - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carbonyl group - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Alkyl fluoride - Hydrocarbon derivative - 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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