Compound Identification
SMILES
CC1=CC=C(C=C1)C(=O)CNC(=O)[C@@H]1C2CCC3=CC4=C(C[C@]3(C)C2=CC[C@H]1C(F)(F)F)C=NN4C1=CC=C(F)C=C1
InChIKey
InChIKey=GLPMFFLLKAOAPD-SCORHKQPSA-N
Formula
C33H31F4N3O2
Mass
577.624
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Steroids and steroid derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Steroids and steroid derivatives
Alternative Parents
Alkyl-phenylketones Phenylpyrazoles Benzoyl derivatives Aryl alkyl ketones Toluenes Fluorobenzenes Aryl fluorides Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Steroid - Alkyl-phenylketone - Phenylpyrazole - Phenylketone - Benzoyl - Aryl ketone - Aryl alkyl ketone - Halobenzene - Fluorobenzene - Toluene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyrazole - Azole - Heteroaromatic compound - Secondary carboxylic acid amide - Ketone - Carboxamide group - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Alkyl fluoride - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alkyl halide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as steroids and steroid derivatives. These are compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred.
External Descriptors
Not available