Compound Identification
SMILES
C[C@@H]1[C@H]2CC[C@@H](C)CN2[C@H]2C[C@H]3[C@@H]4CC[C@H]5CC(=O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12
InChIKey
InChIKey=DCQBOIHKCBTVFH-OWBFZDFVSA-N
Formula
C27H43NO
Mass
397.647
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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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
3-oxo-5-alpha-steroids Azasteroids and derivatives Indolizidines Alkaloids and derivatives Piperidines N-alkylpyrrolidines Trialkylamines Cyclic ketones Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Solanidane skeleton - 3-oxosteroid - Oxosteroid - 3-oxo-5-alpha-steroid - Azasteroid - Indolizidine - Alkaloid or derivatives - Piperidine - N-alkylpyrrolidine - Pyrrolidine - Ketone - Cyclic ketone - Tertiary amine - Tertiary aliphatic amine - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Amine - Organic oxygen compound - 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