Compound Identification
SMILES
C[C@@H]1C2CC[C@H](C)CN2C2CC3C4CC=C5C[C@H](CC[C@]5(C)C4CC[C@]3(C)C12)OCCCN=[N+]=[N-]
InChIKey
InChIKey=BUOQFFJTOKRHAD-UUWPDJQVSA-N
Formula
C30H48N4O
Mass
480.741
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
-
Subclass
Steroidal alkaloids
- Level 5 Solanidines and derivatives
-
Subclass
Steroidal alkaloids
-
Class
Steroids and steroid derivatives
-
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
Delta-5-steroids Azasteroids and derivatives Indolizidines Alkaloids and derivatives Piperidines N-alkylpyrrolidines Trialkylamines Azo imides Azo compounds Dialkyl ethers Azacyclic compounds Organic salts Hydrocarbon derivatives Organic cations
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Solanidane skeleton - Azasteroid - Delta-5-steroid - Alkaloid or derivatives - Indolizidine - Piperidine - N-alkylpyrrolidine - Pyrrolidine - Azo compound - Azo imide - Tertiary aliphatic amine - Tertiary amine - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic salt - Organic cation - 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