Structure Information
Structure

Compound Identification

SMILES

[H][C@](C)(C1=NC[C@]([H])(C)CC1)[C@]1([H])CC[C@]2([H])[C@@]3([H])CC=C4C[C@@]([H])(O)CC[C@@]4(C)[C@]3([H])CC[C@]12C

InChIKey

InChIKey=VRBNGKPRTHBEIQ-IBSFYWHXSA-N

Formula

C27H43NO

Mass

397.647

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Subclass

Steroidal alkaloids

Intermediate Tree Nodes

Not available

Direct Parent

22,26-epiminocholestanes

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

22,26-epiminocholestane skeleton - Progestogin-skeleton - Pregnane-skeleton - 3-hydroxy-delta-5-steroid - 3-hydroxysteroid - Hydroxysteroid - 3-beta-hydroxysteroid - 3-beta-hydroxy-delta-5-steroid - Delta-5-steroid - Tetrahydropyridine - Hydropyridine - Cyclic alcohol - Secondary alcohol - Ketimine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Imine - Organooxygen compound - Organonitrogen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 22,26-epiminocholestanes. These are steroid alkaloids obtained by reduction of spirosolane through opening of the E-ring.

External Descriptors

Not available

Previous Back Next