Structure Information
Structure

Compound Identification

SMILES

C[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(OC(C)=O)C(=O)COP(O)(O)=O

InChIKey

InChIKey=LZQYVDLGJYEPOX-QZIXMDIESA-N

Formula

C24H32FO9P

Mass

514.483

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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

Aliphatic homopolycyclic compounds

Substituents

Progestogin-skeleton - 20-oxosteroid - Steroid ester - Hydroxysteroid - Halo-steroid - 3-oxo-delta-1,4-steroid - Oxosteroid - 9-halo-steroid - 3-oxosteroid - 11-beta-hydroxysteroid - 11-hydroxysteroid - Delta-1,4-steroid - O-acylglycerone-phosphate - Glycerone phosphate - Monoalkyl phosphate - Alpha-acyloxy ketone - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Cyclic alcohol - Ketone - Halohydrin - Carboxylic acid ester - Secondary alcohol - Cyclic ketone - Fluorohydrin - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organohalogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organofluoride - Carbonyl group - Alkyl halide - Alkyl fluoride - Alcohol - Organic oxide - Aliphatic homopolycyclic 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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