Compound Identification
SMILES
C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4CC[C@H]5C[C@@H](N)CC[C@]5(C)[C@H]4CC[C@]23C)N2C[C@H](C)C[C@H](O)[C@H]12
InChIKey
InChIKey=RTCXOPGJLHDJMS-FOWFDDMESA-N
Formula
C27H46N2O
Mass
414.678
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
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Class
Steroids and steroid derivatives
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Subclass
Steroidal alkaloids
- Level 5 Solanidines and derivatives
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Subclass
Steroidal alkaloids
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Class
Steroids and steroid derivatives
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Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Steroidal alkaloids
Intermediate Tree Nodes
Not available
Direct Parent
Solanidines and derivatives
Alternative Parents
Hydroxysteroids Azasteroids and derivatives Indolizidines Alkaloids and derivatives Piperidines N-alkylpyrrolidines Trialkylamines Secondary alcohols 1,2-aminoalcohols Azacyclic compounds Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Solanidane skeleton - 23-hydroxysteroid - Hydroxysteroid - Azasteroid - Indolizidine - Alkaloid or derivatives - Piperidine - N-alkylpyrrolidine - Pyrrolidine - Tertiary amine - Secondary alcohol - Tertiary aliphatic amine - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Alcohol - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - Primary amine - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as solanidines and derivatives. These are steroids with a structure based on the solanidane skeleton. Solanidane arises from the conversion of a cholestane side-chain into a bicyclic system.
External Descriptors
Not available