Compound Identification
SMILES
C[C@H]1C[C@]2(O[C@H]3C[C@H]4[C@@H]5CC[C@H]6C[C@H](O)CC[C@]6(C)[C@H]5C(=O)C[C@]4(C)[C@H]3[C@@]2(C)O)OC1(C)C
InChIKey
InChIKey=PYYCTSSONOEHSO-GORAVFDGSA-N
Formula
C28H44O5
Mass
460.655
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Steroids and steroid derivatives
- Subclass Furospirostanes and derivatives
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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
Furospirostanes and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Furospirostanes and derivatives
Alternative Parents
Triterpenoids Spirostanes and derivatives 3-alpha-hydroxysteroids 11-oxosteroids Ketals Monosaccharides Tetrahydrofurans Tertiary alcohols Secondary alcohols Ketones Cyclic alcohols and derivatives Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Furospirostane-skeleton - Triterpenoid - Spirostane skeleton - 20-hydroxysteroid - 3-hydroxysteroid - Hydroxysteroid - 11-oxosteroid - Oxosteroid - 3-alpha-hydroxysteroid - Ketal - Monosaccharide - Tertiary alcohol - Tetrahydrofuran - Cyclic alcohol - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Organooxygen compound - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as furospirostanes and derivatives. These are heterocyclic steroids containing a furospirostane moiety, which a skeleton characterized by the presence of a 1,6-dioxaspiro[4.4]nonane ring system and an androstane moiety.
External Descriptors
Not available