Structure Information
Structure

Compound Identification

SMILES

CC1=CN(C2CC(N=[N+]=[N-])C(COC(=O)C(O)C3(O)CCC4C5CCC6=CC(=O)C=CC6(C)C5C(O)CC34C)O2)C(=O)NC1=O

InChIKey

InChIKey=IJOGJLMIAFYWOM-UHFFFAOYSA-N

Formula

C31H39N5O9

Mass

625.679

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Subclass

Pregnane steroids

Intermediate Tree Nodes

Not available

Direct Parent

Gluco/mineralocorticoids, progestogins and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Progestogin-skeleton - 20-hydroxysteroid - 3-oxo-delta-1,4-steroid - 3-oxosteroid - Hydroxysteroid - Oxosteroid - 11-beta-hydroxysteroid - 11-alpha-hydroxysteroid - 11-hydroxysteroid - 17-hydroxysteroid - Delta-1,4-steroid - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - Pyrimidone - Hydropyrimidine - Pyrimidine - Vinylogous amide - Cyclic alcohol - Heteroaromatic compound - Tetrahydrofuran - Tertiary alcohol - Cyclic ketone - Azo compound - Azo imide - Carboxylic acid ester - Urea - Ketone - Lactam - Secondary alcohol - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Alcohol - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety.

External Descriptors

Not available

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