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
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Alkaloids and derivatives
- Class Yohimbine alkaloids
-
Superclass
Alkaloids and derivatives
Kingdom
Organic compounds
Superclass
Alkaloids and derivatives
Class
Yohimbine alkaloids
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Yohimbine alkaloids
Alternative Parents
Indoles and derivatives Piperidinones Delta lactams Delta valerolactones Oxanes Benzenoids Organosulfonamides Organic sulfonamides Tertiary carboxylic acid amides Sulfonyls Trihalomethanes Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Organofluorides Organonitrogen compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Alkyl fluorides
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