Compound Identification
SMILES
COC1=NC2=C(C(CO)CN3CCC(C(F)C3)N(CC3=CC=CC=C3)C(O)=O)C(F)=CN=C2C=C1
InChIKey
InChIKey=WPXADJXGEVYMJS-UHFFFAOYSA-N
Formula
C25H28F2N4O4
Mass
486.52
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
Alkyl aryl ethers Aralkylamines Pyridines and derivatives Piperidines Aryl fluorides Benzene and substituted derivatives 1,3-aminoalcohols Heteroaromatic compounds Trialkylamines Carbamic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Alkyl fluorides Organofluorides Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - Alkyl aryl ether - Aralkylamine - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Piperidine - Pyridine - Benzenoid - Heteroaromatic compound - 1,3-aminoalcohol - Tertiary amine - Tertiary aliphatic amine - Carbamic acid - Carbamic acid derivative - Azacycle - Ether - Primary alcohol - Organic oxygen compound - Organohalogen compound - Carbonyl group - Organic oxide - Organofluoride - Organic nitrogen compound - Alcohol - Alkyl halide - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Alkyl fluoride - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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