Compound Identification
SMILES
ON1C=CC2=C3C(=CN=C2C1=O)N(CC1=CC=C(F)C=C1)C=C3C(=O)NCC(F)(F)F
InChIKey
InChIKey=NQMJQNCOKCEILH-UHFFFAOYSA-N
Formula
C20H14F4N4O3
Mass
434.351
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazanaphthalenes
- Subclass Naphthyridines
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Class
Diazanaphthalenes
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Naphthyridines
Intermediate Tree Nodes
Not available
Direct Parent
Naphthyridines
Alternative Parents
Pyrrole carboxamides Fluorobenzenes Pyridinones Aryl fluorides Substituted pyrroles Vinylogous amides Heteroaromatic compounds Lactams Secondary carboxylic acid amides Azacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Organonitrogen compounds Organooxygen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Halobenzene - Pyridinone - Fluorobenzene - Aryl fluoride - Aryl halide - Pyridine - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Vinylogous amide - Secondary carboxylic acid amide - Lactam - Carboxamide group - Carboxylic acid derivative - Azacycle - Organonitrogen compound - Organooxygen compound - Alkyl halide - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organofluoride - Organohalogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
External Descriptors
Not available