Compound Identification
SMILES
Cl.Cl.COC1=NC2=C(CCN3CCC(NCC4=NC=C5OCCOC5=C4)C(O)C3)C(Cl)=CN=C2C=C1
InChIKey
InChIKey=GFVOBHSOIOSFJJ-UHFFFAOYSA-N
Formula
C24H30Cl3N5O4
Mass
558.89
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
2-pyridylmethylamines Alkyl aryl ethers Aminopiperidines Aralkylamines Para dioxins Aryl chlorides Heteroaromatic compounds 1,2-aminoalcohols Secondary alcohols Trialkylamines Dialkylamines Azacyclic compounds Oxacyclic compounds Hydrochlorides Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthyridine - 2-pyridylmethylamine - Alkyl aryl ether - 4-aminopiperidine - Aralkylamine - Aryl chloride - Aryl halide - Para-dioxin - Piperidine - Pyridine - Heteroaromatic compound - Tertiary amine - Secondary alcohol - Tertiary aliphatic amine - 1,2-aminoalcohol - Secondary amine - Oxacycle - Azacycle - Secondary aliphatic amine - Ether - Organic oxygen compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Alcohol - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrochloride - Amine - 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 These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings.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